WO2019083150A1 - Heterocyclic compound, composition comprising same, and organic electronic device comprising same - Google Patents

Abstract

The present specification relates to a heterocyclic compound in chemical formula (1), a composition comprising same, and an organic electronic device comprising same.

Description

HETEROCYCLIC COMPOUND, COMPOSITION CONTAINING SAME, AND ORGANIC ELECTRONIC DEVICE

This application claims the benefit of Korean Patent Application No. 10-2017-0137489, filed on October 23, 2017, to the Korean Intellectual Property Office, the entire contents of which are incorporated herein by reference.

The present invention relates to heterocyclic compounds, compositions comprising them, and organic electronic devices comprising the same.

An organic electronic device means an element requiring charge exchange between an electrode and an organic material using holes and / or electrons. The organic electronic device can be roughly classified into two types according to the operating principle as described below. First, an exciton is formed in an organic material layer by a photon introduced into an element from an external light source. The exciton is separated into an electron and a hole, and the electrons and holes are transferred to different electrodes to be used as a current source Type electric device. The second type is an electronic device that injects holes and / or electrons into an organic semiconductor that interfaces with an electrode by applying a voltage or current to two or more electrodes, and operates by injected electrons and holes.

Examples of the organic electronic device include an organic solar cell, an organic photoelectric device, an organic light emitting device, and an organic transistor. Hereinafter, an organic solar cell will be described in detail. However, in the organic electronic devices, Electron injection or transport materials, or luminescent materials act on a similar principle.

Organic solar cells are important to increase efficiency so that they can output as much electrical energy as possible from solar energy. In order to increase the efficiency of such an organic solar cell, it is also important to generate as much excitons as possible in the semiconductor, but it is also important to draw out generated charges without loss. One of the causes of loss of charge is that the generated electrons and holes are destroyed by recombination. Various methods have been proposed as methods for transferring generated electrons and holes to electrodes without loss, but most of them require additional processing, which may increase the manufacturing cost.

The present invention provides heterocyclic compounds, compositions containing them, and organic electronic devices comprising the same.

The present invention provides a heterocyclic compound represented by the following formula (1).

[Chemical Formula 1]

In Formula 1,

X, X 'and X1 to X6 are the same or different and each independently O, S or Se,

R1 and R2 are the same or different and each independently represents a substituted or unsubstituted straight or branched alkyl group; A substituted or unsubstituted straight or branched alkoxy group; Or a substituted or unsubstituted straight or branched thioalkoxy group,

Y1 and Y2 are the same or different from each other, and each independently hydrogen; A halogen group; A substituted or unsubstituted straight or branched alkyl group; Or a substituted or unsubstituted straight or branched chain alkoxy group,

EW1 and EW2 are the same or different and are each a group independently acting as an electron acceptor,

Ar 1 to Ar 4 are the same or different and each independently represents a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heteroaryl group,

n1 and n2 are each 0 or 1,

When n1 and n2 are 0 and R1 and R2 are the same or different and are each independently a substituted or unsubstituted linear or branched alkyl group, Y1 and Y2 are the same or different from each other, group; A substituted or unsubstituted straight or branched alkyl group; Or a substituted or unsubstituted straight-chain or branched alkoxy group.

The present invention provides a composition for an organic electronic device comprising the above heterocyclic compound.

Also, the present specification discloses a plasma display panel comprising a first electrode; A second electrode facing the first electrode; And at least one organic material layer provided between the first electrode and the second electrode, wherein at least one of the organic material layers includes the above-mentioned organic electronic device composition do.

The organic electronic device including the heterocyclic compound represented by Formula 1 according to one embodiment of the present invention has excellent photoelectric conversion efficiency.

1 is a view showing an organic electronic device according to an embodiment of the present invention.

2 is a diagram showing NMR data of Compound 1 according to one embodiment of the present invention.

3 shows NMR data of compound 2 according to one embodiment of the present invention.

4 shows NMR data of compound 3 according to one embodiment of the present invention.

5 shows NMR data of compound 4 according to one embodiment of the present invention.

6 is a diagram showing UV-vis absorption spectra in a solution state of the compounds 1 to 4 according to one embodiment of the present invention.

7 is a diagram showing UV-vis absorption spectra in the film state of the compounds 1 to 4 according to one embodiment of the present invention.

8 is a diagram showing UV-vis absorption spectra in a solution state of Compound 1 according to one embodiment of the present invention and Comparative Example Compound 2 (ITIC2).

9 is a diagram showing UV-vis absorption spectra in a solution state of Compound 3 and Comparative Compound 2 (ITIC2) according to one embodiment of the present invention.

10 is a diagram showing UV-vis absorption spectra in a solution state of Compound 5 according to one embodiment of the present invention and Comparative Example Compound 2 (ITIC2).

[Description of Symbols]

10: first electrode

20: Second electrode

30: photoactive layer

100: Organic electronic device

Hereinafter, the present specification will be described in detail.

The present invention provides a heterocyclic compound represented by the above formula (1).

According to one embodiment of the present invention, the heterocyclic compound represented by Formula 1 may have a substituent such as an alkyl group, an alkoxy group, a S-Alkyl group, and / or a fluorine, When the heterocyclic compound is used as an n-type organic compound layer (electron acceptor material) of the photoactive layer of an organic solar cell with a low open-circuit voltage and a high LUMO energy, a high open-circuit voltage (V _oc ) And has a photo-electric conversion efficiency.

According to one embodiment of the present invention, the heterocyclic compound represented by the general formula (1) is a heterocyclic compound in which R1 and R2 are alkyl groups, and Y1 and Y2 include substituents other than hydrogen, especially fluorine, Absorbed. Accordingly, the organic solar cell including the same exhibits a short circuit current higher than that of an organic solar cell including a compound in which R1 and R2 in the formula (1) are alkyl groups and Y1 and Y2 are hydrogen.

In this specification, when a part is referred to as " including " an element, it is to be understood that it may include other elements as well, without departing from the other elements unless specifically stated otherwise.

In this specification, when a member is located on another member, it includes not only the case where the member is in contact with the other member but also the case where another member exists between the two members.

Examples of such substituents are described below, but are not limited thereto.

The term " substituted " means that the hydrogen atom bonded to the carbon atom of the compound is replaced with another substituent, and the substituted position is not limited as long as the substituent is a substitutable position, , Two or more substituents may be the same or different from each other.

As used herein, the term " substituted or unsubstituted " A halogen group; An alkyl group; An alkenyl group; An alkoxy group; Thioalkoxy groups; Ester group; A carbonyl group; A carboxyl group; A hydroxy group; A cycloalkyl group; Silyl group; An arylalkenyl group; An aryloxy group; An alkyloxy group; An alkylsulfoxy group; Arylsulfoxy group; Boron group; An alkylamine group; An aralkylamine group; An arylamine group; A heterocyclic group; An arylamine group; An aryl group; A nitrile group; A nitro group; A hydroxy group; And a heteroaryl group containing at least one of N, O and S atoms, or does not have any substituent (s).

The substituents may be substituted or unsubstituted with an additional substituent.

In the present specification, the halogen group may be fluorine, chlorine, bromine or iodine.

In the present specification, the number of carbon atoms of the imide group is not particularly limited, but is preferably 1 to 25 carbon atoms. Specifically, it may be a compound having the following structure, but is not limited thereto.

In the present specification, the amide group may be mono- or di-substituted by nitrogen of the amide group with hydrogen, a straight-chain, branched-chain or cyclic alkyl group having 1 to 25 carbon atoms or an aryl group having 6 to 25 carbon atoms. Specifically, it may be a compound of the following structural formula, but is not limited thereto.

In the present specification, the alkyl group may be linear or branched, and the number of carbon atoms is not particularly limited, but is preferably 1 to 50. Specific examples include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec- N-pentyl, 3-dimethylbutyl, 2-ethylbutyl, heptyl, n-hexyl, Cyclohexylmethyl, octyl, n-octyl, tert-octyl, 1-methylheptyl, 2-ethylhexyl, 2-propylpentyl, n-nonyl, 2,2-dimethyl Heptyl, 1-ethyl-propyl, 1,1-dimethyl-propyl, isohexyl, 2-methylpentyl, 4-methylhexyl and 5-methylhexyl.

In the present specification, the cycloalkyl group is not particularly limited, but preferably has 3 to 60 carbon atoms. Specific examples thereof include cyclopropyl, cyclobutyl, cyclopentyl, 3-methylcyclopentyl, 2,3-dimethylcyclopentyl, But are not limited to, 3-methylcyclohexyl, 4-methylcyclohexyl, 2,3-dimethylcyclohexyl, 3,4,5-trimethylcyclohexyl, 4-tert- butylcyclohexyl, cycloheptyl and cyclooctyl Do not.

In the present specification, the alkoxy group may be linear, branched or cyclic. The number of carbon atoms of the alkoxy group is not particularly limited, but is preferably 1 to 20 carbon atoms. Specific examples include methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, tert-butoxy, sec-butoxy, n-pentyloxy, neopentyloxy, isopentyloxy, n Butyloxy, n-octyloxy, n-nonyloxy, n-decyloxy, benzyloxy and p-methylbenzyloxy, and the like. But is not limited thereto.

In the present specification, the thioalkoxy group can be applied to the description of the alkoxy group except that O of the alkoxy group is S.

In the present specification, the alkenyl group may be straight-chain or branched, and the number of carbon atoms is not particularly limited, but is preferably 2 to 40. Specific examples include vinyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, Butenyl, allyl, 1-phenylvinyl-1-yl, 2-phenylvinyl-1-yl, (Diphenyl-1-yl) vinyl-1-yl, stilbenyl, and styrenyl groups.

In the present specification, the silyl group specifically includes a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a vinyldimethylsilyl group, a propyldimethylsilyl group, a triphenylsilyl group, a diphenylsilyl group, But are not limited thereto.

In the present specification, the boron group may be -BRR ', wherein R and R' are the same or different and each independently hydrogen; heavy hydrogen; A halogen group; A nitrile group; A substituted or unsubstituted monocyclic or polycyclic cycloalkyl group having 3 to 30 carbon atoms; A substituted or unsubstituted, straight or branched chain alkyl group having 1 to 30 carbon atoms; A substituted or unsubstituted monocyclic or polycyclic aryl group having 6 to 30 carbon atoms; And a substituted or unsubstituted monocyclic or polycyclic heteroaryl group having 2 to 30 carbon atoms.

In the present specification, the phosphine oxide group specifically includes a diphenylphosphine oxide group, a dinaphthylphosphine oxide group, and the like, but is not limited thereto.

In the present specification, the aryl group may be a monocyclic aryl group or a polycyclic aryl group, and includes a case where an alkyl group having 1 to 25 carbon atoms or an alkoxy group having 1 to 25 carbon atoms is substituted. In addition, an aryl group in the present specification may mean an aromatic ring.

When the aryl group is a monocyclic aryl group, the number of carbon atoms is not particularly limited, but is preferably 6 to 25 carbon atoms. Specific examples of the monocyclic aryl group include phenyl group, biphenyl group, terphenyl group, and the like, but are not limited thereto.

When the aryl group is a polycyclic aryl group, the number of carbon atoms is not particularly limited. And preferably has 10 to 24 carbon atoms. Specific examples of the polycyclic aryl group include, but are not limited to, a naphthyl group, an anthracenyl group, a phenanthryl group, a pyrenyl group, a perylenyl group, a klycenyl group and a fluorenyl group.

In the present specification, a fluorenyl group is a structure in which two cyclic organic compounds are connected through one atom.

In the present specification, the fluorenyl group may be substituted, and adjacent substituents may be bonded to each other to form a ring.

등이 될 수 있다. 다만, 이에 한정되는 것은 아니다.When the fluorenyl group is substituted,

And the like. However, the present invention is not limited thereto.

In the present specification, the heteroaryl group is a heteroaryl group containing at least one of O, N and S as a hetero atom. The number of carbon atoms is not particularly limited, but is preferably 2 to 60 carbon atoms. Examples of the heteroaryl group include a selenophene group, a thiophene group, a furan group, a pyrrolyl group, an imidazole group, a thiazole group, an oxazole group, an oxadiazole group, a pyridyl group, a bipyridyl group, a pyrimidyl group, , An acridyl group, a pyridazinyl group, a pyrazinyl group, a quinolinyl group, a quinazolinyl group, a quinoxalinyl group, a phthalazinyl group, a pyridopyrimidinyl group, a pyridopyranyl group, a pyrazinopyranyl group, A benzofuranyl group, a benzofuranyl group, a phenanthroline group, an isoxazolyl group, an imidazolyl group, an indole group, a carbazole group, a benzoxazole group, a benzimidazole group, a benzothiazole group, a benzocarbazole group, a benzothiophene group, A thiadiazolyl group, a benzothiadiazolyl group, a phenothiazinyl group, a thienothiophene group, and a dibenzofuranyl group, but the present invention is not limited thereto.

In the present specification, the hydrocarbon ring may be an aromatic, aliphatic or aromatic and aliphatic condensed ring, and may be selected from the examples of the cycloalkyl group or the aryl group except the univalent hydrocarbon ring.

In this specification, the aromatic ring may be monocyclic or polycyclic and may be selected from the examples of the aryl group except that it is not monovalent.

In the present specification, the hetero ring includes one or more non-carbon atoms and hetero atoms. Specifically, the hetero atom may include one or more atoms selected from the group consisting of O, N, Se, and S, and the like. The heterocyclic ring may be monocyclic or polycyclic, and may be an aromatic, aliphatic or aromatic and aliphatic condensed ring, and examples thereof may be selected from the heteroaryl group or the heterocyclic group except that the monocyclic group is not monovalent.

In the present specification, an electron donative group (EDG) or an electron donor substance is generally a substituent or substance having a pair of negative or non-covalent electrons and means donating electrons to a portion lacking a positive charge or electron pair. Further, in the present specification, an electron donative group (EDG) or an electron donor substance may have a negative electron retaining property when the light is received in a state mixed with an electron acceptor, And a substituent capable of transferring excited electrons to an electron acceptor having a high electronegativity.

In this specification, an electron withdrawing group (EWG) or an electron acceptor material acting as an electron acceptor means a substituent or substance which accepts electrons from an electron hole excitation.

According to one embodiment of the present invention, in the above formula (1), n1 is 0.

According to one embodiment of the present invention, in the above formula (1), n1 is 1.

According to one embodiment of the present invention, in the above formula (1), n2 is 0.

According to one embodiment of the present invention, in the above formula (1), n2 is 1.

According to one embodiment of the present invention, in the above formula (1), X is O.

According to one embodiment of the present invention, in the above formula (1), X is S.

According to one embodiment of the present invention, in the above formula (1), X is Se.

According to one embodiment of the present invention, in the above formula (1), X 'is O.

According to one embodiment of the present invention, in the above formula (1), X 'is S.

According to one embodiment of the present invention, in the above formula (1), X 'is Se.

According to one embodiment of the present invention, in the above formula (1), X1 is O.

According to one embodiment of the present invention, in the above formula (1), X1 is S.

According to one embodiment of the present invention, in the above formula (1), X1 is Se.

According to one embodiment of the present invention, in the above formula (1), X2 is O.

According to one embodiment of the present disclosure, X2 in Formula 1 is S.

According to one embodiment of the present invention, in the above formula (1), X2 is Se.

According to one embodiment of the present invention, in the above formula (1), X3 is O.

According to one embodiment of the present invention, in the above formula (1), X3 is S.

According to one embodiment of the present invention, in the above formula (1), X3 is Se.

According to one embodiment of the present invention, in the above formula (1), X4 is O.

According to one embodiment of the present invention, in the above formula (1), X4 is S.

According to one embodiment of the present invention, in the above formula (1), X4 is Se.

According to one embodiment of the present invention, in the above formula (1), X5 is O.

According to one embodiment of the present invention, in the above formula (1), X5 is S.

According to one embodiment of the present invention, in the above formula (1), X5 is Se.

According to one embodiment of the present invention, in the above formula (1), X6 is O.

According to one embodiment of the present invention, in the above formula (1), X6 is S.

According to one embodiment of the present invention, in the above formula (1), X6 is Se.

According to one embodiment of the present invention, the formula (1) is represented by Formula 1-1 or Formula 1-2.

[Formula 1-1]

[Formula 1-2]

In the above formulas 1-1 and 1-2,

R1, R2, Y1, Y2, and Ar1 to Ar4 have the same meanings as defined in Formula 1,

Cy1 and Cy2 are the same or different and each independently represents an aromatic hydrocarbon ring substituted or unsubstituted with a halogen group, a linear or branched alkyl group, or a linear or branched alkoxy group; Or a halogen group, a straight chain or branched alkyl group, or a substituted or unsubstituted heterocycle with a straight or branched chain alkoxy group.

According to one embodiment of the present invention, the formula (1) is represented by any one of the following formulas (1-3) to (1-5).

[Formula 1-3]

[Formula 1-4]

[Formula 1-5]

In Formulas 1-3 to 1-5 above,

Y1, Y2 and Ar1 to Ar4 have the same meanings as defined in formula (1)

R11 and R12 are the same or different and each independently represents a substituted or unsubstituted straight or branched alkyl group,

Y11 and Y12 are the same or different and are each independently a halogen group,

Cy1 and Cy2 are the same or different and each independently represents an aromatic hydrocarbon ring substituted or unsubstituted with a halogen group, a linear or branched alkyl group, or a linear or branched alkoxy group; Or a halogen group, a straight chain or branched alkyl group, or a substituted or unsubstituted heterocycle with a straight or branched chain alkoxy group.

According to another embodiment of the present invention, R11 and R12 are the same or different and are each independently a straight chain or branched alkyl group.

According to another embodiment of the present invention, R11 and R12 are the same or different and are each independently a branched chain alkyl group.

According to another embodiment of the present invention, R11 and R12 are the same or different and are each independently a branched chain alkyl group having 3 to 20 carbon atoms.

According to another embodiment of the present invention, R11 and R12 are the same or different and are each independently a branched chain alkyl group having 3 to 10 carbon atoms.

According to another embodiment of the present invention, R11 and R12 are the same or different from each other, and each independently is a 2-ethylhexyl group.

According to another embodiment of the present disclosure, Y11 and Y12 are fluorine.

According to one embodiment of the present invention, R 1 and R 2 in the general formula (1) are the same or different and each independently represents a linear or branched alkyl group; A linear or branched alkoxy group; Or a straight or branched thioalkoxy group.

According to one embodiment of the present invention, in the general formula (1), R 1 and R 2 are the same or different and each independently represents a branched chain alkyl group; A branched chain alkoxy group; Or a branched thioalkoxy group.

According to one embodiment of the present invention, in the general formula (1), R 1 and R 2 are the same or different and each independently represents a branched chain alkyl group having 3 to 20 carbon atoms; A branched chain alkoxy group having 3 to 20 carbon atoms; Or a branched chain thioalkoxy group having 3 to 20 carbon atoms.

According to one embodiment of the present invention, in the general formula (1), R1 and R2 are the same or different and each independently represents a branched alkyl group having 3 to 10 carbon atoms; A branched chain alkoxy group having 3 to 10 carbon atoms; Or a branched thioalkoxy group having 3 to 10 carbon atoms.

According to one embodiment of the present invention, in the general formula (1), R 1 and R 2 are the same or different and are each independently a 2-ethylhexyl group; 2-ethylhexyloxy group; Or a 2-ethylhexylthio group.

According to one embodiment of the present invention, in Formula 1, Y1 and Y2 are the same or different from each other, and each independently hydrogen; Or a halogen group.

According to one embodiment of the present invention, in Formula 1, Y1 and Y2 are the same or different from each other, and each independently hydrogen; Or fluorine.

According to one embodiment of the present invention, in the general formula (1), Y1 and Y2 are hydrogen.

According to one embodiment of the present invention, in the general formula (1), Y1 and Y2 are fluorine.

According to one embodiment of the present invention, in the general formula (1), Y1 is hydrogen.

According to one embodiment of the present invention, in the general formula (1), Y2 is hydrogen.

According to one embodiment of the present invention, in the general formula (1), Y1 is fluorine.

According to one embodiment of the present invention, in the general formula (1), Y2 is fluorine.

According to one embodiment of the present invention, in the general formula (1), n1 and n2 are 0, R1 and R2 are the same or different and each independently represents a linear or branched alkyl group, Y1 and Y2 are the same Or different, and each independently represents a halogen group.

According to one embodiment of the present invention, in the general formula (1), n1 and n2 are 0, R1 and R2 are the same or different and each independently represents a branched chain alkyl group, and Y1 and Y2 are fluorine.

According to one embodiment of the present invention, in the general formula (1), n1 and n2 are 0, R1 and R2 are the same or different and each independently represents a branched alkyl group having 3 to 20 carbon atoms, Y1 and Y2 Is fluorine.

According to one embodiment of the present invention, in the general formula (1), n1 and n2 are 0, R1 and R2 are the same or different and each independently represents a branched alkyl group having 3 to 10 carbon atoms, Y1 and Y2 Is fluorine.

According to one embodiment of the present invention, in the general formula (1), n1 and n2 are 0, R1 and R2 are 2-ethylhexyl groups, and Y1 and Y2 are fluorine.

According to one embodiment of the present invention, EW1 and EW2 are the same or different and are each independently represented by the following formula (a).

(A)

In the above formula (a)

Cy1 represents an aromatic hydrocarbon ring substituted or unsubstituted with a halogen group, a linear or branched alkyl group, or a linear or branched alkoxy group; Or a halogen group, a straight chain or branched chain alkyl group, or a substituted or unsubstituted heterocycle with a straight chain or branched chain alkoxy group,

는 상기 화학식 1에 결합되는 부위이다.

Is a moiety bonded to the formula (1).

According to one embodiment of the present invention, in the formula (a), Cy1 is a benzene ring substituted or unsubstituted with a halogen group, a straight chain or branched chain alkyl group, or a straight chain or branched chain alkoxy group; Thienothiophene ring; Dibenzothiophene ring; Or a thiophene ring which is substituted or unsubstituted with a halogen group, a straight chain or branched chain alkyl group, or a straight chain or branched chain alkoxy group.

According to one embodiment of the present invention, in the formula (a), Cy1 represents a benzene ring substituted or unsubstituted with a fluorine, a methyl group, or a methoxy group; Thienothiophene ring; Dibenzothiophene ring; Or a thiophene ring substituted or unsubstituted with a methyl group.

According to one embodiment of the present disclosure, EW1 and EW2 are the same or different and independently selected from the following structures.

The structures of EW1 and EW2 control the energy level of Formula 1, that is, the absorption wavelength of light, and the organic solar cell including the EW1 and EW2 has a synergistic effect of the regulated voltage V _oc and the short-circuit current J _sc . Specifically, when Cy1 in the formula (a) is a benzene ring substituted with a halogen group, the light absorption region moves to a longer wavelength side to obtain a high short-circuit current. When Cy1 is a benzene ring substituted with an alkyl group, LUMO energy The level is increased and a high open-circuit voltage can be obtained.

According to one embodiment of the present invention, Ar 1 to Ar 4 are the same or different from each other and each independently represents a linear or branched alkyl group, a linear or branched alkoxy group, or a linear or branched thio An aryl group substituted or unsubstituted with an alkoxy group; Or a straight or branched alkyl group, a straight chain or branched alkoxy group, or a heteroaryl group substituted or unsubstituted with a linear or branched thioalkoxy group.

According to one embodiment of the present invention, Ar 1 to Ar 4 are the same or different from each other and each independently represents a linear or branched alkyl group, a linear or branched alkoxy group, or a linear or branched thio A substituted or unsubstituted phenyl group with an alkoxy group; A linear or branched alkyl group, a linear or branched alkoxy group, or a furan group substituted or unsubstituted with a linear or branched thioalkoxy group; A linear or branched alkyl group, a linear or branched alkoxy group, or a thio group substituted or unsubstituted with a linear or branched thioalkoxy group; Or a linear or branched alkyl group, a linear or branched alkoxy group, or a selenophen group substituted or unsubstituted with a linear or branched thioalkoxy group.

According to one embodiment of the present invention, Ar 1 to Ar 4 are the same or different and are each independently a phenyl group substituted or unsubstituted with a linear or branched alkyl group; A furan group substituted or unsubstituted with a linear or branched alkyl group; Thiophene groups substituted or unsubstituted with straight or branched chain alkyl groups; Or a selenophen group substituted or unsubstituted with a linear or branched alkyl group.

According to one embodiment of the present invention, Ar 1 to Ar 4 are the same or different from each other and are each independently a phenyl group substituted or unsubstituted with a linear or branched alkyl group having 1 to 30 carbon atoms; A furan group substituted or unsubstituted with a straight or branched alkyl group having 1 to 30 carbon atoms; A thiophene group substituted or unsubstituted with a straight or branched alkyl group having 1 to 30 carbon atoms; Or a selenophen group substituted or unsubstituted with a straight or branched alkyl group having 1 to 30 carbon atoms.

According to one embodiment of the present invention, in the general formula (1), Ar 1 to Ar 4 are the same or different and each independently represents a phenyl group substituted or unsubstituted with a straight or branched alkyl group having 1 to 10 carbon atoms; A furan group substituted or unsubstituted with a straight or branched alkyl group having 1 to 1 carbon atoms; A thiophene group substituted or unsubstituted with a straight or branched alkyl group having 1 to 1 carbon atoms; Or a selenophen group substituted or unsubstituted with a linear or branched alkyl group having 1 to 10 carbon atoms.

According to one embodiment of the present invention, in the general formula (1), Ar 1 to Ar 4 are the same or different and each is a phenyl group substituted with an n-hexyl group; a furan group substituted with an n-hexyl group; a thiophene group substituted with an n-hexyl group; Or a selenophen group substituted with an n-hexyl group.

According to one embodiment of the present invention, in the general formula (1), Ar1 to Ar4 are the same or different and independently selected from the following structures.

In the above structure,

X " is S, O or Se,

R 100 and R 101 are the same or different from each other and each independently represents a linear or branched alkyl group, a linear or branched alkoxy group, or a linear or branched thioalkoxy group,

는 상기 화학식 1에 결합되는 부위이다.

Is a moiety bonded to the formula (1).

According to another embodiment of the present invention, R100 and R101 are the same or different and are each independently a linear or branched alkyl group.

According to another embodiment of the present invention, R100 and R101 are the same or different and each independently is a straight or branched alkyl group having 1 to 30 carbon atoms.

According to another embodiment of the present invention, R100 and R101 are the same or different and each independently is a straight or branched alkyl group having 1 to 10 carbon atoms.

According to another embodiment of the present invention, R100 and R101 are n-hexyl groups.

According to one embodiment of the present invention, in the general formula (1), Ar1 to Ar4 are the same or different and independently selected from the following structures.

In the above structures, R100 and R101 are the same as described above.

According to one embodiment of the present invention, in the general formula (1), Ar1 to Ar4 are the same or different and independently selected from the following structures.

The structures of Ar1 to Ar4 control the extinction coefficient of Formula 1, and organic solar cells containing the same control a high short circuit current. In the above structure, it is possible to control the HOMO and LUMO energy levels according to the substitution position (para or meta) of the substituted alkyl group in the phenyl group, the thiophene and the thienothiophene, It can bring about a voltage increasing effect. In addition, the position of the substituted alkyl group in the phenyl group, thiophene and thienothiophene can induce the arrangement of molecules in the film state, which is favorable for devices of the organic solar cell, The battery exhibits high short circuit current and charge rate.

According to one embodiment of the present disclosure, Formula 1 is selected from the following compounds.

The present invention provides a composition for an organic electronic device comprising the heterocyclic compound represented by the above formula (1).

According to one embodiment of the present invention, the composition for organic electronic devices includes an electron donor material and an electron acceptor material, and the electron acceptor material includes the heterocyclic compound.

In addition, most of electron donor substances having the maximum absorption wavelength in the visible light region can be applied to the electron donor substance in the organic electronic device composition, but the present invention is not limited thereto.

According to one embodiment of the present invention, the electron donor material may be a material used in the art, for example, poly-3-hexyl thiophene (P3HT), poly [N- 2'-heptadecanyl-2,7-carbazole-alt-5,5- (4'-7'-di-2-thienyl-2 ', 1', 3'- benzothiadiazole)], PCPDTBT (poly [ Cyclopenta [2,1-b; 3,4-b '] dithiophene) -tallow-4,7- (2,1,3-benzothiadiazole) ), PFO-DBT (poly [2,7- (9,9-dioctyl-fluorene) -alt-5,5- (4,7-di 2-thienyl-2,1,3-benzothiadiazole) (PTB7-Th) (Poly [[4,8-bis [(2-ethylhexyl) oxy] benzo [1,2- b: 4,5- b '] dithiophene-2,6- 2- [(2-ethylhexyl) carbonyl] thieno [3,4-b] thiophenediyl]]), PSiF-DBT (Poly [2,7- (9,9-dioctyldibenzosilole) -bis (thiophen-2-yl) benzo-2,1,3-thiadiazole] and poly (benzodithiophene-benzotriazole) (PBDB-T).

According to an embodiment of the present invention, the composition for organic electronic devices includes an electron donor material and an electron acceptor material, and is contained in a weight ratio of 1:99 to 99: 1.

According to one embodiment of the specification, the photoactive layer comprises an electron donor material and an electron acceptor material, and is included in a weight ratio of 1: 5 to 5: 1.

According to one embodiment of the present disclosure, the electron donor and the electron acceptor constitute a bulk heterojunction (BHJ).

According to one embodiment of the present invention, the composition for organic electronic devices may further comprise a solvent.

In one embodiment of the present invention, the composition for organic electronic devices may be a liquid. The " liquid phase " means that the liquid phase is at normal temperature and pressure.

In one embodiment of the present invention, the solvent includes, for example, chlorinated solvents such as chloroform, methylene chloride, 1,2-dichloroethane, 1,1,2-trichloroethane, chlorobenzene and o-dichlorobenzene; Ether solvents such as tetrahydrofuran and dioxane; Aromatic hydrocarbon solvents such as toluene, xylene, trimethylbenzene and mesitylene; Aliphatic hydrocarbon solvents such as cyclohexane, methylcyclohexane, n-pentane, n-hexane, n-heptane, n-octane, n-nonane and n-decane; Ketone solvents such as acetone, methyl ethyl ketone, and cyclohexanone; Ester solvents such as ethyl acetate, butyl acetate and ethyl cellosolve acetate; Examples of polyhydric alcohols such as ethylene glycol, ethylene glycol monobutyl ether, ethylene glycol monoethyl ether, ethylene glycol monomethyl ether, dimethoxyethane, propylene glycol, diethoxymethane, triethylene glycol monoethyl ether, glycerin, Alcohols and their derivatives; Alcohol solvents such as methanol, ethanol, propanol, isopropanol, and cyclohexanol; Sulfoxide-based solvents such as dimethylsulfoxide; And amide solvents such as N-methyl-2-pyrrolidone and N, N-dimethylformamide; Benzoate solvents such as methyl benzoate, butyl benzoate and 3-phenoxy benzoate; A solvent such as tetralin is exemplified, but a solvent capable of dissolving or dispersing the compound according to one embodiment of the present specification is sufficient, and the solvent is not limited thereto.

In another embodiment, the solvents may be used alone or in combination of two or more solvents.

In another embodiment, the boiling point of the solvent is preferably 40 ° C to 250 ° C, more preferably 60 ° C to 230 ° C, but is not limited thereto.

In another embodiment, the viscosity of the single or mixed solvent is preferably 1 CP to 10 CP, more preferably 3 CP to 8 CP, but is not limited thereto.

In another embodiment, the concentration of the composition for organic electronic devices is preferably 0.1 wt / v% to 20 wt / v%, more preferably 0.5 wt / v% to 5 wt / v% It is not limited.

According to one embodiment of the present invention, the composition for organic electronic devices further comprises an additive.

According to one embodiment of the present disclosure, the molecular weight of the additive is from 50 g / mol to 1000 g / mol.

According to one embodiment of the present invention, the additive is included in an amount of 0.1 to 10 parts by weight based on the composition for organic electronics.

In another embodiment, the boiling point of the additive is an organic matter of 30 占 폚 to 300 占 폚.

In this specification, an organic substance means a substance containing at least one carbon atom.

In one embodiment, the additive is selected from the group consisting of 1,8-diiodooctane (DIO), 1-chloronaphthalene (1-CN), diphenylether One or two additives among additives selected from the group consisting of octane dithiol, tetrabromothiophene, and the like.

The present invention provides an organic electronic device formed using the composition for an organic electronic device.

The present disclosure relates to a plasma display panel comprising a first electrode; A second electrode facing the first electrode; And at least one organic compound layer disposed between the first electrode and the second electrode, wherein at least one of the organic compound layers includes the composition for the organic electronic device.

According to one embodiment of the present invention, the organic electronic device is selected from the group consisting of an organic photoelectric device, an organic transistor, an organic solar cell, and an organic light emitting device.

According to one embodiment of the present invention, the organic electronic device may be an organic solar cell.

According to one embodiment of the present disclosure, there is provided a liquid crystal display comprising: a first electrode; A second electrode facing the first electrode; And at least one organic compound layer disposed between the first electrode and the second electrode, wherein at least one of the organic compound layers includes the organic electronic device composition.

According to one embodiment of the present invention, the organic layer includes a photoactive layer, and the photoactive layer includes the composition for the organic electronic device.

According to one embodiment of the present invention, the photoactive layer includes the composition for organic electronic devices, the composition for the organic electronic device includes the above-mentioned heterocyclic compound, and the band gap of the heterocyclic compound is 1 eV to 3 eV, specifically 1 eV to 2 eV, and even more specifically 1 eV to 1.6 eV.

The bandgap measured the HOMO and LUMO energy levels through cyclic voltammetry (CV), and the difference between the HOMO and LUMO energy levels is the bandgap. Cyclic voltammetry (CV) measures 0.1 M [nBu ₄ N] ⁺ [PF ₆ ] ^- using glassy carbon as a working electrode through an acetonitrile solution, It is not.

An organic solar cell according to an embodiment of the present invention includes a first electrode, a photoactive layer, and a second electrode. The organic solar cell may further include a substrate, a hole transporting layer, and / or an electron transporting layer.

According to one embodiment of the present invention, when the organic solar cell receives photons from an external light source, electrons and holes are generated between the electron beams and the electron acceptors. The generated holes are transported to the anode through the electron donor layer.

FIG. 1 is a view illustrating an organic electronic device according to an embodiment of the present invention. The first electrode 10, the photoactive layer 30, and the second electrode 20 are stacked in this order. And an additional organic material layer may be provided between the first electrode 10 and the second electrode 20.

According to one embodiment of the present disclosure, the organic solar cell may further include an additional organic layer. The organic solar cell can reduce the number of organic layers by using organic materials having various functions at the same time.

According to one embodiment of the present disclosure, the first electrode is an anode and the second electrode is a cathode. In another embodiment, the first electrode is a cathode and the second electrode is an anode.

According to one embodiment of the present disclosure, the organic solar cell may be arranged in the order of the cathode, the photoactive layer, and the anode, and may be arranged in the order of the anode, the photoactive layer, and the cathode.

In another embodiment, the organic solar cell may be arranged in the order of an anode, a hole transporting layer, a photoactive layer, an electron transporting layer and a cathode, and may be arranged in the order of a cathode, an electron transporting layer, a photoactive layer, a hole transporting layer, , But is not limited thereto.

According to one embodiment of the present invention, the organic solar cell has a normal structure. In the normal structure, the substrate, the anode, the organic material layer including the photoactive layer, and the cathode may be stacked in this order.

According to one embodiment of the present invention, the organic solar cell is an inverted structure. In the inverted structure, the substrate, the cathode, the organic material layer including the photoactive layer, and the anode may be stacked in this order.

According to one embodiment of the present invention, the organic solar cell is a tandem structure.

The organic solar cell according to one embodiment of the present disclosure may have one photoactive layer or two or more layers. In the tandem structure, two or more photoactive layers may be included.

In another embodiment, a buffer layer may be provided between the photoactive layer and the hole transporting layer or between the photoactive layer and the electron transporting layer. At this time, a hole injection layer may be further provided between the anode and the hole transport layer. Further, an electron injecting layer may be further provided between the cathode and the electron transporting layer.

In this specification, the substrate may be a glass substrate or a transparent plastic substrate having excellent transparency, surface smoothness, ease of handling, and waterproofness, but is not limited thereto, and is not limited as long as it is a substrate commonly used in organic solar cells. Specific examples include glass or polyethylene terephthalate, polyethylene naphthalate (PEN), polypropylene (PP), polyimide (PI), and triacetyl cellulose (TAC) But is not limited thereto.

The anode electrode may be a transparent material having excellent conductivity, but is not limited thereto. Metals such as vanadium, chromium, copper, zinc, and gold, or alloys thereof; Metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO); ZnO: Al or SnO _2: a combination of a metal and an oxide such as Sb; And conductive polymers such as poly (3-methylthiophene), poly [3,4- (ethylene-1,2-dioxy) thiophene] (PEDOT), polypyrrole and polyaniline, but are not limited thereto .

The method of forming the anode electrode is not particularly limited and may be applied to one surface of the substrate or may be coated in a film form using, for example, sputtering, E-beam, thermal evaporation, spin coating, screen printing, inkjet printing, doctor blade or gravure printing . ≪ / RTI >

When the anode electrode is formed on a substrate, it may undergo cleaning, moisture removal and hydrophilic reforming processes.

For example, the patterned ITO substrate is sequentially washed with a cleaning agent, acetone, and isopropyl alcohol (IPA), and then dried on a heating plate at 100 ° C to 150 ° C for 1 to 30 minutes, preferably 120 ° C for 10 minutes And when the substrate is completely cleaned, the surface of the substrate is hydrophilically modified.

Through such surface modification, the junction surface potential can be maintained at a level suitable for the surface potential of the photoactive layer. Further, in the modification, the formation of the polymer thin film on the anode electrode is facilitated, and the quality of the thin film may be improved.

Pretreatment techniques for the anode electrode include a) surface oxidation using a parallel plate discharge, b) a method of oxidizing the surface through ozone generated using UV ultraviolet radiation in vacuum, and c) oxygen radicals generated by the plasma And the like.

One of the above methods can be selected depending on the state of the anode electrode or the substrate. However, whichever method is used, it is preferable to prevent oxygen from escaping from the surface of the anode electrode or the substrate and to suppress the residual of moisture and organic matter as much as possible. At this time, the substantial effect of the pretreatment can be maximized.

As a specific example, a method of oxidizing the surface through ozone generated using UV can be used. At this time, the ITO substrate patterned after the ultrasonic cleaning is baked on a hot plate, dried well, then put into a chamber, and is irradiated with ozone generated by reaction of oxygen gas with UV light by operating a UV lamp The patterned ITO substrate can be cleaned.

However, the method of modifying the surface of the patterned ITO substrate in the present specification is not particularly limited, and any method may be used as long as it is a method of oxidizing the substrate.

The cathode electrode may be a metal having a small work function, but is not limited thereto. Specifically, metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin and lead or alloys thereof; Or a multilayer structure material such as LiF / Al, LiO ₂ / Al, LiF / Fe, Al: Li, Al: BaF ₂ and Al: BaF ₂ : Ba.

The cathode may be deposited in a thermal evaporator having a degree of vacuum of 5 x 10 ^{< -7} > torr or less, but the method is not limited thereto.

The hole transporting layer and / or the electron transporting layer material efficiently transfer electrons and holes separated from the photoactive layer to the electrode, and the material is not particularly limited.

The hole transport layer material may include poly (3,4-ethylenediocythiophene) doped with poly (styrenesulfonic acid) (PEDOT: PSS), molybdenum oxide (MoO _x ); Vanadium oxide (V ₂ O ₅ ); Nickel oxide (NiO); And tungsten oxide (WO _x ), but the present invention is not limited thereto.

The electron transport layer material may be electron-extracting metal oxides, specifically a metal complex of 8-hydroxyquinoline; Complexes containing Alq ₃ ; Metal complexes including Liq; LiF; Ca; Titanium oxide (TiO _x ); Zinc oxide (ZnO); And cesium carbonate (Cs ₂ CO ₃ ), but the present invention is not limited thereto.

The photoactive layer may be formed by applying the composition for an organic electronic device on a substrate by spin coating, dip coating, screen printing, spray coating, doctor blade, brush painting, roll to roll printing, inkjet printing, nozzle printing, offset printing, Screen printing, or the like. However, the present invention is not limited to these methods.

The composition for an organic electronic device according to one embodiment of the present invention is advantageous in terms of time and cost in manufacturing a device because a solution process is suitable for its structural characteristics.

Since the composition for organic electronic devices includes the heterocyclic compound of Formula 1, the photoactive layer has a uniform photoelectric conversion efficiency within a thickness range of 50 nm to 150 nm.

According to one embodiment of the present disclosure, the thickness of the photoactive layer is 50 nm to 150 nm, specifically 100 nm to 150 nm.

In one embodiment of the present disclosure, the organic electronic device may be an organic transistor.

According to one embodiment of the present disclosure, an organic transistor including a source, a drain, a gate, and one or more organic layers, wherein at least one of the organic layers includes the heterocyclic compound.

According to one embodiment of the present invention, the organic layer includes an n-type semiconductor layer and a p-type semiconductor layer, and the n-type semiconductor layer includes the heterocyclic compound.

The production method of the heterocyclic compound and the production of the organic electronic device including the same will be described in detail in the following Production Examples and Examples. However, the following examples are intended to illustrate the present specification, and the scope of the present specification is not limited thereto.

PREPARATION EXAMPLE 1 Preparation of Compound 1

1) Preparation of Compound A-1

(4,8-bis (5 - ((2-ethylhexyl) thio) thiophen-2-yl) benzo [1,2- b: 4,5- b '] dithiophene- 6-diyl) bis (trimethylstannane) ) 6 g, ethyl 2-bromo-thiophene-3-carboxylate 3.28g (2.5eq), Pd 2 (dba) 3 0.27g (0.05eq) , and tri (o-tolyl) phosphine 0.30 g (0.1 eq) was dissolved in toluene and refluxed for 12 hours. The reaction was terminated through dichloromethane, extracted with distilled water, and then purified by column chromatography to obtain Compound A-1.

2) Preparation of Compound A-2

7.28 g (5.3 eq) of 1-bromo-4-hexyl-benzene was dissolved in tetrahydrofuran, and 12.08 mL (1.0 eq) of n-butyllithium was slowly added to the flask and stirred at the same temperature for 1 hour Respectively. Thereafter, Compound A-1 (5.3 g) was dissolved in tetrahydrofuran and slowly injected. After stirring for 12 hours at room temperature, the reaction was completed through distilled water, extracted with dichloromethane, purified by column chromatography, and refluxed under acetic acid / HCl (40 mL / 0.5 mL) A-2 was obtained.

3) Preparation of Compound A-3

Compound A-2 (2.6 g) was dissolved in tetrahydrofuran in a round-bottomed flask, and 2.0 mL (2.5 eq) of n-butyllithium was slowly added thereto at -78 ° C. and stirred at the same temperature for 1 hour. Then 0.39 mL of dimethylformamide was slowly added. After stirring for 12 hours at room temperature, the reaction was completed through distilled water and purified by column chromatography to obtain Compound A-3.

4) Preparation of compound 1

Compound A-3 (0.4 g) and 3- (Dicyanomethylidene) indan-1-one (0.2 g, 5 eq) were dissolved in chloroform in a round flask equipped with a condenser and refluxed at 65 ° C after the addition of 1 ml of pyridine. After 12 hours, the solid produced by methanol was purified by column chromatography to give compound 1.

Fig. 2 shows NMR data of the above compound 1. Fig.

PREPARATION EXAMPLE 2 Preparation of Compound 2

Compound A-3 (0.4 g) and 0.23 g (5 eq) of 2- (5,6-difluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene) malononitrile were added to a round- After dissolving in chloroform, 1 mL of pyridine was added and refluxed at 65 ° C. After 12 h, the solid produced by methanol was purified by column chromatography to give compound 2. < 1 >

Fig. 3 is a diagram showing NMR data of the compound 2. Fig.

PREPARATION EXAMPLE 3 Preparation of Compound 3

1) Preparation of compound B-1

To a round bottomed flask equipped with a condenser was added (4,8-bis (5- (2-ethylhexyl) -4-fluorothiophen-2-yl) benzo [1,2- b: 4,5- b '] dithiophene -2,6-diyl) bis (trimethylstannane) ((4,8-bis (5- (2-ethylhexyl) -4-fluorothiophen- b '] dithiophene-2,6-diyl ) bis (trimethylstannane)) 6 g, ethyl 2-bromo-thiophene-3-carboxylate 3.28g (2.5eq), Pd 2 (dba) 3 0.27g (0.05eq), and 0.30 g (0.1 eq) of tri (o-tolyl) phosphine was dissolved in toluene and refluxed for 12 hours. The reaction was terminated through dichloromethane, extracted with distilled water, and then purified by column chromatography to obtain Compound B-1.

2) Preparation of compound B-2

8.12 g (5.3 eq) of 1-bromo-4-hexyl-benzene was dissolved in tetrahydrofuran and 12.08 mL (1.0 eq) of n-butyllithium was slowly injected into a round flask and stirred at the same temperature for 1 hour Respectively. Compound B-1 (5.3 g) was then dissolved in tetrahydrofuran and slowly injected. After stirring for 12 hours at room temperature, the reaction was terminated through distilled water, extracted with dichloromethane, purified by column chromatography, and refluxed for 4 hours under acetic acid / HCl (40 mL / 0.5 mL) to obtain compound B-2 .

3) Preparation of compound B-3

Compound B-2 (2.0 g) was dissolved in tetrahydrofuran in a round-bottomed flask, and 2.0 mL (2.5 eq) of n-butyllithium was slowly added thereto at -78 ° C. and stirred at the same temperature for 1 hour. Then 0.45 mL of dimethylformamide was slowly added. After stirring for 12 hours at room temperature, the reaction was completed through distilled water and purified by column chromatography to obtain Compound B-3

4) Preparation of Compound 3

Compound B-3 (0.4 g) and 3- (Dicyanomethylidene) indan-1-one (0.2 g, 5 eq) were dissolved in chloroform in a round flask equipped with a condenser and refluxed at 65 ° C after the addition of 1 ml of pyridine. After 12 h, the solid produced by methanol was purified by column chromatography to give compound 3.

4 is a diagram showing NMR data of the compound 3.

Preparation Example 4 Preparation of Compound 4

(0.4 g) and 0.23 g (5 eq) of 2- (5,6-difluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene) malononitrile were added to a round- After dissolving in chloroform, 1 mL of pyridine was added and refluxed at 65 ° C. After 12 hours, the solid produced by methanol was purified by column chromatography to give compound 4.

5 is a graph showing NMR data of the above-mentioned compound 4. FIG.

FIG. 6 is a diagram showing UV-vis absorption spectra of the compounds 1 to 4 in the solution state, and FIG. 7 is a diagram showing UV-vis absorption spectra of the compounds 1 to 4 in the film state.

6 shows data obtained by measuring the UV-vis absorption spectrum of each of the compounds 1 to 4 after dissolving the compounds 1 to 4 in chlorobenzene. FIG. 7 shows the data obtained by dissolving each of the compounds 1 to 4 in chlorobenzene and spin- And UV-vis absorption spectrum after the preparation.

PREPARATION EXAMPLE 5 Preparation of Compound 5

2-yl) benzo [1,2-b: 4,5-b '] dithiophene-2,6-diyl (prepared as described in Preparation Example 1 bis (5 - ((2-ethylhexyl) oxy) thiophen-2-yl) benzo [1,2- b: 4,5- b '] dithiophene- diyl) bis (trimethylstannane) was used instead of bis (trimethylstannane).

≪ Comparative Example Compound 1 (BT-IC) >

≪ Comparative Example Compound 2 (ITIC2) >

Comparative Examples 1 and 2 were purchased from Solarmer materials Inc. and used.

Table 1 below shows the physical properties of the compounds 1 to 4 and the comparative compounds 1 and 2. 6 and 7, and the physical properties of the comparative compounds 1 and 2 were measured using the comparative compounds 1 and 2 in place of the compound 1, respectively, as shown in FIGS. 6 and 7, The UV-vis spectra of the solution and film states were measured and the following results were obtained.

Solution Film OpticalE _g ^opt (eV) ? _{max , abs} (nm) ? _max (nm) lambda _edge (nm) Compound 1 670 704 794 1.56 Compound 2 683 711 809 1.53 Compound 3 678 579 779 1.59 Compound 4 691 623 786 1.57 Comparative Example Compound 1 700 711 800 1.55 Comparative Example Compound 2 714 738 810 1.53

In Table 1, Solution λ _max denotes the maximum absorption wavelength in the solution state, Film λ _max denotes the maximum absorption wavelength in the film state, Film λ _edge denotes the absorption _edge in the film state, and Optical E _g ^opt denotes the optical band gap do. As shown in Table 1, the compounds 1 to 4 are excellent in the ability to attract electrons, and thus can absorb light in the longer wavelength regions of Comparative Examples 1 and 2.

Comparative Example 1-1. Manufacture of organic solar cell

A composite solution was prepared by dissolving the following compound PBDB-T and Comparative Example Compound 1 (BT-IC) in 1: 2 in chlorobenzene (CB). At this time, the concentration was adjusted to 2 wt / vol%, stirred at 700 rpm overnight, and 0.25% of diphenylether (DPE) was added to the complex solution and annealed at 100 ° C to 120 ° C. The organic solar cell has an inverted structure of ITO / ZnO NP / photoactive layer / MoO ₃ / Ag.

The glass substrate (11.5 Ω / □) coated with a 1.5 cm × 1.5 cm bar type ITO was ultrasonically cleaned using distilled water, acetone, and 2-propanol, and the ITO surface was subjected to ozone treatment for 10 minutes ZnO NP (ZnO nanograde N-10 2.5 wt% in 1-butanol, filtered to 0.45 μm PTFE) was spin coated on the ZnO NP solution at 4000 rpm for 40 seconds, The remaining solvent was removed by heat treatment to complete the electron transport layer. For the coating of the photoactive layer, the annealed composite solution was spin-coated at 1500 rpm for 15 seconds. In the thermal evaporator, MoO ₃ was thermally deposited at a rate of 0.2 Å / s at 10 ^-7 Torr to a thickness of 10 nm to prepare a hole transport layer. In this order, Ag was deposited in a thermal evaporator at a rate of 1 Å / s to form a 100 nm organic solar cell.

[PBDB-T]

Comparative Example 1-2. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Comparative Example 1-1, except that the composite solution was spin-coated at 1700 rpm instead of 1500 rpm for coating the photoactive layer in Comparative Example 1-1.

Comparative Examples 1-3. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Comparative Example 1-1, except that the composite solution was spin-coated at 1900 rpm instead of 1500 rpm for coating the photoactive layer in Comparative Example 1-1.

Comparative Examples 1-4. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Comparative Example 1-1, except that the composite solution was spin-coated at 2200 rpm instead of 1500 rpm for coating the photoactive layer in Comparative Example 1-1.

The light-to-electricity conversion characteristics of the organic solar cells prepared in Comparative Examples 1-1 to 1-4 were measured under the conditions of 100 mW / cm ² (AM 1.5), and the results are shown in Table 2 below.

Spin-speed (rpm) V _oc (V) J _sc (mA / cm ² ) FF 侶 (%) Mean η (%) Comparative Example 1-1 1500 1.027 13.289 0.550 7.50 7.44 1.023 13.140 0.549 7.37 Comparative Example 1-2 1700 1.030 13.286 0.567 7.75 7.75 - - - - Comparative Example 1-3 1900 1.030 13.539 0.592 8.26 8.19 1.028 13.220 0.597 8.11 Comparative Example 1-4 2200 1.030 13.340 0.610 8.38 8.41 1.026 13.620 0.603 8.43

Comparative Example 2-1. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Comparative Example 1-1, except that the compound of Comparative Example 2 (ITIC2) was used instead of the compound of Comparative Example 1 in Comparative Example 1-1.

Comparative Example 2-2. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Comparative Example 1-2, except that the compound of Comparative Example 2 (ITIC2) was used instead of the compound of Comparative Example 1 in Comparative Example 1-2.

Comparative Example 2-3. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Comparative Example 1-3, except that the compound of Comparative Example 2 (ITIC2) was used instead of the compound of Comparative Example 1 in Comparative Example 1-3.

Comparative Example 2-4. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Comparative Example 1-4, except that the compound of Comparative Example 2 (ITIC2) was used instead of the compound of Comparative Example 1 in Comparative Example 1-4.

The light-to-electricity conversion characteristics of the organic solar cells prepared in Comparative Examples 2-1 to 2-4 were measured under the conditions of 100 mW / cm ² (AM 1.5), and the results are shown in Table 3 below.

Spin-speed (rpm) V _oc (V) J _sc (mA / cm ² ) FF (%) η (%) Mean η (%) Comparative Example 2-1 1500 1.021 13.870 0.586 8.30 8.19 1.017 14.232 0.557 8.07 Comparative Example 2-2 1700 1.024 13.775 0.582 8.22 8.59 1.018 14.853 0.592 8.95 Comparative Example 2-3 1900 1.028 14.635 0.602 9.07 9.18 1.024 14.720 0.616 9.29 Comparative Example 2-4 2200 1.023 13.914 0.620 8.83 8.87 1.021 14.230 0.613 8.91

Example 1-1. Manufacture of organic solar cell

In Comparative Example 1-1, the compound 1 was used instead of the Comparative Example Compound 1, and the compound solution prepared by using Compound 1 instead of the Comparative Example Compound 1 was spin-coated at 1000 rpm instead of 1500 rpm. An organic solar cell was prepared in the same manner as in 1-1.

Examples 1-2. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 1-1, except that the composite solution was spin-coated at 1200 rpm instead of 1000 rpm in Example 1-1.

Examples 1-3. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 1-1, except that the composite solution was spin-coated at 1400 rpm instead of 1000 rpm in Example 1-1.

Examples 1-4. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 1-1, except that the composite solution was spin-coated at 1600 rpm instead of 1000 rpm in Example 1-1.

Examples 1-5. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 1-1, except that the composite solution was spin-coated at 1800 rpm instead of 1000 rpm in Example 1-1.

Examples 1-6. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 1-1, except that the composite solution was spin-coated at 2000 rpm instead of 1000 rpm in Example 1-1.

The light-to-electricity conversion characteristics of the organic solar cells prepared in Examples 1-1 to 1-6 were measured under the conditions of 100 mW / cm ² (AM 1.5), and the results are shown in Table 4 below.

Spin-speed (rpm) V _oc (V) J _sc (mA / cm ² ) FF (%) η (%) Mean η (%) Example 1-1 1000 0.917 15.654 0.739 10.60 10.41 0.916 15.163 0.736 10.22 Examples 1-2 1200 0.912 15.198 0.726 10.06 9.90 0.907 14.647 0.733 9.73 Example 1-3 1400 0.914 13.305 0.737 8.97 9.22 0.911 13.933 0.746 9.47 Examples 1-4 1600 0.913 13.379 0.746 9.11 9.09 0.910 13.383 0.745 9.07 Examples 1-5 1800 0.910 13.132 0.744 8.89 9.09 0.907 13.772 0.744 9.29 Examples 1-6 2000 0.898 12.880 0.724 8.37 8.29 0.902 12.235 0.743 8.21

Example 2-1. Manufacture of organic solar cell

In Comparative Example 1-1, the compound 2 was used in place of the Comparative Example Compound 1, and the compound solution prepared by using Compound 2 instead of the Comparative Example Compound 1 was spin-coated at 800 rpm instead of 1500 rpm. An organic solar cell was prepared in the same manner as in 1-1.

Example 2-2. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 2-1 except that the complex solution was spin-coated at 1000 rpm instead of 800 rpm in Example 2-1.

Examples 2-3. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 2-1 except that the composite solution was spin-coated at 1200 rpm instead of 800 rpm in Example 2-1.

Examples 2-4. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 2-1, except that the composite solution was spin-coated at 1400 rpm instead of 800 rpm in Example 2-1.

Examples 2-5. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 2-1 except that the composite solution was spin-coated at 1600 rpm instead of 800 rpm in Example 2-1.

The light-to-electricity conversion characteristics of the organic solar cells prepared in Examples 2-1 to 2-5 were measured under the conditions of 100 mW / cm ² (AM 1.5), and the results are shown in Table 5 below

Spin-speed (rpm) V _oc (V) J _sc (mA / cm ² ) FF (%) η (%) Mean η (%) Example 2-1 800 0.896 16.173 0.681 9.87 9.78 0.885 16.248 0.673 9.68 Example 2-2 1000 0.889 16.464 0.703 10.29 10.38 0.890 16.796 0.700 10.46 Example 2-3 1200 0.887 16.080 0.708 10.10 10.39 0.885 17.294 0.698 10.68 Examples 2-4 1400 0.891 15.483 0.711 9.81 9.90 0.887 15.981 0.705 9.99 Example 2-5 1600 0.884 15.481 0.717 9.82 9.82 0.887 15.467 0.716 9.82

Example 3-1. Manufacture of organic solar cell

In Comparative Example 1-1, the compound 3 was used in place of the Comparative Example Compound 1, and the compound solution prepared by using Compound 3 instead of the Comparative Example Compound 1 was spin-coated at 800 rpm instead of 1500 rpm. An organic solar cell was prepared in the same manner as in 1-1.

Example 3-2. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 3-1 except that the composite solution was spin-coated at 1000 rpm instead of 800 rpm in Example 3-1.

Example 3-3. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 3-1, except that the composite solution was spin-coated at 1200 rpm instead of 800 rpm in Example 3-1.

Example 3-4. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 3-1, except that the composite solution was spin-coated at 1400 rpm instead of 800 rpm in Example 3-1.

Examples 3-5. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 3-1, except that the composite solution was spin-coated at 1600 rpm instead of 800 rpm in Example 3-1.

The light-to-electricity conversion characteristics of the organic solar cells prepared in Examples 3-1 to 3-5 were measured at 100 mW / cm ² (AM 1.5), and the results are shown in Table 6 below.

Spin-speed (rpm) V _oc (V) J _sc (mA / cm ² ) FF (%) 侶 (%) Mean η (%) Example 3-1 800 0.853 16.132 0.669 9.20 9.23 0.851 16.508 0.659 9.26 Example 3-2 1000 0.856 15.895 0.680 9.24 9.32 0.856 15.843 0.693 9.39 Example 3-3 1200 0.849 15.137 0.697 8.96 9.04 0.845 15.487 0.696 9.11 Example 3-4 1400 0.849 15.018 0.699 8.92 8.91 0.847 14.925 0.705 8.90 Example 3-5 1600 0.849 14.443 0.706 8.65 8.73 0.846 14.574 0.714 8.81

Example 4-1. Manufacture of organic solar cell

In Comparative Example 1-1, the compound 4 was used instead of the Comparative Example Compound 1, and the compound solution prepared by using Compound 4 instead of the Comparative Example Compound 1 was spin-coated at 1000 rpm instead of 1500 rpm. An organic solar cell was prepared in the same manner as in 1-1.

Example 4-2. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 4-1 except that the composite solution was spin-coated at 1200 rpm instead of 1000 rpm in Example 4-1.

Example 4-3. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 4-1 except that the complex solution was spin-coated at 1400 rpm instead of 1000 rpm in Example 4-1.

Example 4-4. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 4-1, except that the composite solution was spin-coated at 1600 rpm instead of 1000 rpm in Example 4-1.

The light-to-electricity conversion characteristics of the organic solar cell prepared in Examples 4-1 to 4-4 were measured under the conditions of 100 mW / cm ² (AM 1.5), and the results are shown in Table 7 below.

Spin-speed (rpm) V _oc (V) J _sc (mA / cm ² ) FF (%) η (%) Mean η (%) Example 4-1 1000 0.893 15.852 0.705 9.97 9.97 - - - - Example 4-2 1200 0.895 15.829 0.704 9.98 9.99 0.889 15.778 0.713 10.00 Example 4-3 1400 0.894 15.318 0.696 9.53 9.83 0.886 16.118 0.710 10.13 Example 4-4 1600 0.893 15.519 0.713 9.89 9.97 0.891 15.714 0.718 10.04

As a result of Tables 2 to 7, the organic solar cell including the heterocyclic compound represented by Formula 1 according to one embodiment of the present invention has an open circuit voltage, a charge rate And the light-to-electricity conversion efficiency is excellent.

Comparative Example 3-1. Manufacture of organic solar cell

The compound PBDB-T and the comparative compound 2 (ITIC2) were dissolved in chlorobenzene (CB) at a ratio of 1: 2 to prepare a composite solution. At this time, the concentration was adjusted to 2 wt / vol%, stirred at 700 rpm overnight, and 0.5% of 1,8-diiodooctane (DIO: 1,8-diiodooctane) 0.0 > 120 C < / RTI > The organic solar cell has an inverted structure of ITO / ZnO NP / photoactive layer / MoO ₃ / Ag.

The glass substrate (11.5 Ω / □) coated with a 1.5 cm × 1.5 cm bar type ITO was ultrasonically cleaned using distilled water, acetone, and 2-propanol, and the ITO surface was subjected to ozone treatment for 10 minutes ZnO NP (ZnO nanograde N-10 2.5 wt% in 1-butanol, filtered to 0.45 μm PTFE) was spin coated on the ZnO NP solution at 4000 rpm for 40 seconds, The remaining solvent was removed by heat treatment to complete the electron transport layer. For the coating of the photoactive layer, the annealed composite solution was spin-coated at 800 rpm for 15 seconds. In the thermal evaporator, MoO ₃ was thermally deposited at a rate of 0.2 Å / s at 10 ^-7 Torr to a thickness of 10 nm to prepare a hole transport layer. In this order, Ag was deposited in a thermal evaporator at a rate of 1 Å / s to form a 100 nm organic solar cell.

Comparative Example 3-2. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Comparative Example 3-1, except that the composite solution was spin-coated at 1000 rpm instead of 800 rpm for coating the photoactive layer in Comparative Example 3-1.

Comparative Example 3-3. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Comparative Example 3-1, except that the composite solution was spin-coated at 1200 rpm instead of 800 rpm for coating the photoactive layer in Comparative Example 3-1.

Comparative Example 3-4. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Comparative Example 3-1, except that the composite solution was spin-coated at 1400 rpm instead of 800 rpm for coating the photoactive layer in Comparative Example 3-1.

Example 5-1. Manufacture of organic solar cell

In Comparative Example 3-1, the compound 1 was used in place of the Comparative Example Compound 2, and the compound solution prepared by using the compound 1 instead of the Comparative Example Compound 2 was spin-coated at 900 rpm instead of 800 rpm. An organic solar cell was prepared in the same manner as in 3-1.

Example 5-2. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 5-1 except that the composite solution was spin-coated at 1000 rpm instead of 900 rpm for coating the photoactive layer in Example 5-1.

Example 5-3. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 5-1 except that the composite solution was spin-coated at 1100 rpm instead of 900 rpm for coating the photoactive layer in Example 5-1.

Example 5-4. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 5-1, except that the composite solution was spin-coated at 1200 rpm instead of 900 rpm for coating the photoactive layer in Example 5-1.

8 is a diagram showing the UV-vis absorption spectrum in the solution state of the compound 1 and the comparative compound 2 (ITIC2).

Specifically, FIG. 8 is data obtained by dissolving each of the compound 1 and the comparative compound 2 (ITIC2) in chlorobenzene and measuring the UV-vis absorption spectrum.

In FIG. 8, it was confirmed that the UV-Vis absorption region of Compound 1 was shifted toward longer wavelength than that of Comparative Example Compound 2 by the introduction of thioalkoxy. In FIG. 8, the 720 nm shoulder peak in the UV-Vis absorption spectrum of the compound 1 can be seen as evidence that it is superior to the compound of the comparative example 2 by π-π stacking, and that the hole / electron mobility of the molecule itself is excellent This can be indirect evidence. This is an important factor for high short circuit current in organic solar cells.

The light-to-electricity conversion characteristics of the organic solar cells prepared in Comparative Examples 3-1 to 3-4 and Examples 5-1 to 5-4 were measured under the conditions of 100 mW / cm ² (AM 1.5) 8 shows the results.

Spin-speed (rpm) V _oc (V) J _sc (mA / cm ² ) FF 侶 (%) Mean η (%) Comparative Example 3-1 800 0.941 12.427 0.613 7.17 7.47 0.943 13.388 0.614 7.76 Comparative Example 3-2 1000 0.953 13.422 0.628 8.04 8.01 0.948 13.140 0.641 7.98 Comparative Example 3-3 1200 0.953 12.747 0.642 7.80 7.69 0.898 12.250 0.688 7.58 Comparative Example 3-4 1400 0.951 12.124 0.654 7.54 7.41 0.940 11.910 0.649 7.27 Example 5-1 900 0.903 15.876 0.648 9.28 9.18 0.901 15.765 0.639 9.08 Example 5-2 1000 0.897 16.246 0.630 9.18 9.31 0.895 16.520 0.638 9.43 Example 5-3 1100 0.902 16.189 0.662 9.67 9.56 0.898 16.193 0.649 9.44 Examples 5-4 1200 0.892 15.891 0.650 9.21 9.35 0.891 16.078 0.663 9.49

In Table 8, the compound 1 containing the thioalkoxy group absorbs light of a longer wavelength region than that of the compound of the Comparative Example 2, so that the organic solar cell to which it is applied has a high short-circuit current of 15.5 mA / cm ² or more, Conversion efficiency.

Example 6-1. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Comparative Example 3-1, except that the compound 3 was used instead of the compound 2 (ITIC2) in Comparative Example 3-1.

Example 6-2. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 6-1, except that the composite solution was spin-coated at 1000 rpm instead of 800 rpm for coating the photoactive layer in Example 6-1.

Example 6-3. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 6-1, except that the composite solution was spin-coated at 1200 rpm instead of 800 rpm for coating the photoactive layer in Example 6-1.

Example 6-4. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 6-1, except that the composite solution was spin-coated at 1400 rpm instead of 800 rpm for coating the photoactive layer in Example 6-1.

9 is a diagram showing UV-vis absorption spectra in the solution state of the compound 3 and the comparative compound 2 (ITIC2).

Specifically, FIG. 9 is data obtained by dissolving each of the compound 3 and the comparative compound 2 (ITIC2) in chlorobenzene and measuring the UV-vis absorption spectrum.

In FIG. 9, it can be seen that the introduction of the F atom in the compound 3 shown in FIG. 9 indicates that the UV-Vis absorption region is shifted to a longer wavelength side than the Comparative Compound 2, and this is an important factor for exhibiting a high short-circuit current in the organic solar cell.

The light-to-electricity conversion characteristics of the organic solar cells prepared in Comparative Examples 3-1 to 3-4 and Examples 6-1 to 6-4 were measured under the conditions of 100 mW / cm ² (AM 1.5) 9 shows the results.

Spin-speed (rpm) V _oc (V) J _sc (mA / cm ² ) FF 侶 (%) Mean η (%) Comparative Example 3-1 800 0.941 12.427 0.613 7.17 7.47 0.943 13.388 0.614 7.76 Comparative Example 3-2 1000 0.953 13.422 0.628 8.04 8.01 0.948 13.140 0.641 7.98 Comparative Example 3-3 1200 0.953 12.747 0.642 7.80 7.69 0.898 12.250 0.688 7.58 Comparative Example 3-4 1400 0.951 12.124 0.654 7.54 7.41 0.940 11.910 0.649 7.27 Example 6-1 800 0.896 15.976 0.651 9.32 9.32 Example 6-2 1000 0.890 16.125 0.658 9.44 9.32 0.884 16.258 0.640 9.20 Example 6-3 1200 0.890 15.849 0.655 9.23 9.07 0.884 15.225 0.662 8.91 Example 6-4 1400 0.891 14.998 0.672 8.98 8.43 0.872 13.914 0.649 7.88

In Table 9, the compound 3 containing F absorbs light of a longer wavelength region than that of the compound of Comparative Example 2, so that the organic solar cell to which it is applied has a high short circuit current of 13.9 mA / cm ² or more and a high light- Conversion efficiency.

Example 7-1. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 5-1, except that Compound 5 was used instead of Compound 3 in Example 5-1.

Example 7-2. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 7-1, except that the composite solution was spin-coated at 1000 rpm instead of 800 rpm for coating the photoactive layer in Example 7-1.

Example 7-3. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 7-1, except that the composite solution was spin-coated at 1200 rpm instead of 800 rpm for coating the photoactive layer in Example 7-1.

Example 7-4. Manufacture of organic solar cell

An organic solar cell was prepared in the same manner as in Example 7-1, except that the composite solution was spin-coated at 1400 rpm instead of 800 rpm for coating the photoactive layer in Example 7-1.

10 is a diagram showing the UV-vis absorption spectrum in the solution state of the compound 5 and the comparative compound 2 (ITIC2).

Specifically, FIG. 10 is data obtained by dissolving the compound 5 and the comparative compound 2 (ITIC2) in chlorobenzene and measuring the UV-vis absorption spectrum.

In FIG. 10, it was confirmed that the UV-Vis absorption region of Compound 5 was shifted toward longer wavelength than that of Comparative Example Compound 2 by the introduction of an alkoxy group.

In addition, it can be seen that oxygen atoms having excellent electron donating ability are introduced and the long wavelength shift range of the UV-Vis spectrum is large. This is an important factor for high short circuit current in organic solar cells.

The light-to-electricity conversion characteristics of the organic solar cells prepared in Comparative Examples 3-1 to 3-4 and Examples 7-1 to 7-4 were measured under the conditions of 100 mW / cm ² (AM 1.5) 10 shows the results.

Spin-speed (rpm) V _oc (V) J _sc (mA / cm ² ) FF 侶 (%) Mean η (%) Comparative Example 3-1 800 0.941 12.427 0.613 7.17 7.47 0.943 13.388 0.614 7.76 Comparative Example 3-2 1000 0.953 13.422 0.628 8.04 8.01 0.948 13.140 0.641 7.98 Comparative Example 3-3 1200 0.953 12.747 0.642 7.80 7.69 0.898 12.250 0.688 7.58 Comparative Example 3-4 1400 0.951 12.124 0.654 7.54 7.41 0.940 11.910 0.649 7.27 Example 7-1 800 0.910 16.294 0.638 9.46 9.54 0.908 16.279 0.651 9.62 Example 7-2 1000 0.896 16.082 0.649 9.34 9.34 - - - - Example 7-3 1200 0.906 16.134 0.649 9.49 9.49 - - - - Example 7-4 1400 0.878 15.819 0.616 8.55 8.74 0.878 15.998 0.636 8.93

In Table 10, the compound 5 containing the alkoxy group absorbs light of a longer wavelength region than that of the compound of the Comparative Example 2, so that the organic solar cell to which it is applied has a high short circuit current of 15.5 mA / cm ² or more and a high light- Conversion efficiency. In the Tables 2 to 10, V _oc denotes an open-circuit voltage, J _sc denotes a short-circuit current, FF denotes a fill factor, and PCE (η) denotes energy conversion efficiency. The open-circuit voltage and the short-circuit current are the X-axis and Y-axis intercepts in the fourth quadrant of the voltage-current density curve, respectively. The higher the two values, the higher the efficiency of the solar cell. The fill factor is the width of the rectangle that can be drawn inside the curve divided by the product of the short-circuit current and the open-circuit voltage. The energy conversion efficiency can be obtained by dividing these three values by the intensity of the irradiated light, and a higher value is preferable.

Claims (14)

A heterocyclic compound represented by the following formula (1): [Chemical Formula 1]

In Formula 1, X, X 'and X1 to X6 are the same or different and each independently O, S or Se, R1 and R2 are the same or different and each independently represents a substituted or unsubstituted straight or branched alkyl group; A substituted or unsubstituted straight or branched alkoxy group; Or a substituted or unsubstituted straight or branched thioalkoxy group, Y1 and Y2 are the same or different from each other, and each independently hydrogen; A halogen group; A substituted or unsubstituted straight or branched alkyl group; Or a substituted or unsubstituted straight or branched chain alkoxy group, EW1 and EW2 are the same or different and are each a group independently acting as an electron acceptor, Ar 1 to Ar 4 are the same or different and each independently represents a substituted or unsubstituted aryl group; Or a substituted or unsubstituted heteroaryl group, n1 and n2 are each 0 or 1, When n1 and n2 are 0 and R1 and R2 are the same or different and are each independently a substituted or unsubstituted linear or branched alkyl group, Y1 and Y2 are the same or different from each other, group; A substituted or unsubstituted straight or branched alkyl group; Or a substituted or unsubstituted straight-chain or branched alkoxy group. [3] The method of claim 1, wherein R1 and R2 are the same or different and each independently represents a branched alkyl group; A branched chain alkoxy group; Or a branched thioalkoxy group. 2. The compound according to claim 1, wherein Y1 and Y2 are the same or different from each other, and each independently hydrogen; Or a halogen group. The compound according to claim 1, wherein Ar 1 to Ar 4 are the same or different and each independently represents a linear or branched alkyl group, a linear or branched alkoxy group, or an aryl group substituted or unsubstituted with a linear or branched thioalkoxy group ; Or a heteroaryl group substituted or unsubstituted with a linear or branched alkyl group, a straight-chain or branched alkoxy group, or a straight-chain or branched thioalkoxy group. The heterocyclic compound according to claim 1, wherein EW1 and EW2 are the same or different and are each independently a group represented by the following formula (a): (A)

In the above formula (a) Cy1 represents an aromatic hydrocarbon ring substituted or unsubstituted with a halogen group, a linear or branched alkyl group, or a linear or branched alkoxy group; Or a halogen group, a straight chain or branched chain alkyl group, or a substituted or unsubstituted heterocycle with a straight chain or branched chain alkoxy group,

Is a moiety bonded to the formula (1). The heterocyclic compound according to claim 1, wherein the formula 1 is represented by the following formula 1-1 or 1-2: [Formula 1-1]

[Formula 1-2]

In the above formulas 1-1 and 1-2, R1, R2, Y1, Y2, and Ar1 to Ar4 have the same meanings as defined in Formula 1, Cy1 and Cy2 are the same or different and each independently represents an aromatic hydrocarbon ring substituted or unsubstituted with a halogen group, a linear or branched alkyl group, or a linear or branched alkoxy group; Or a halogen group, a straight chain or branched alkyl group, or a substituted or unsubstituted heterocycle with a straight or branched chain alkoxy group. The heterocyclic compound according to claim 1, wherein the formula (1) is selected from the following compounds:

A composition for an organic electronic device comprising the heterocyclic compound according to any one of claims 1 to 7. [Claim 9] The composition for an organic electronic device according to claim 8, wherein the composition for an organic electronic device comprises an electron donor material and an electron acceptor material, and the electron acceptor material comprises the heterocyclic compound. The composition for an organic electronic device according to claim 9, wherein the electron donor material and the electron acceptor material constitute bulk heterojunction (BHJ). A first electrode; A second electrode facing the first electrode; And And at least one organic material layer provided between the first electrode and the second electrode, Wherein at least one of the organic material layers comprises the composition for an organic electronic device according to claim 8. 12. The organic electronic device according to claim 11, wherein the organic electronic device is selected from the group consisting of an organic photoelectric device, an organic transistor, an organic solar cell, and an organic light emitting device. 12. The organic electroluminescent device according to claim 11, wherein the organic electronic device comprises: a first electrode; A second electrode facing the first electrode; And And at least one organic material layer provided between the first electrode and the second electrode, Wherein at least one of the organic material layers comprises the composition for organic electronic devices. 14. The organic electronic device according to claim 13, wherein the organic layer comprises a photoactive layer, and the photoactive layer comprises the composition for organic electronics.

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