[go: up one dir, main page]

Zhu et al., 2021 - Google Patents

Asymmetrical planar acridine-based hole-transporting materials for highly efficient perovskite solar cells

Zhu et al., 2021

Document ID
4133861911632243588
Author
Zhu X
Wu F
Peng C
Ding L
Yu Y
Jiang Z
Zhu L
Liao L
Publication year
Publication venue
Chemical Engineering Journal

External Links

Snippet

Abstract Here, the asymmetrical 8, 8-dimethyl-8H-indolo [3, 2, 1-de] acridine (ACZ) is firstly developed as central core for hole-transporting materials (HTMs) in perovskite solar cells (PeSCs). Two asymmetrical HTMs N 3, N 3, N 6, N 6, N 10, N 10-hexakis (4-methoxyphenyl) …
Continue reading at www.sciencedirect.com (other versions)

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/54Material technologies
    • Y02E10/549Material technologies organic PV cells
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/54Material technologies
    • Y02E10/542Dye sensitized solar cells
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/005Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0062Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
    • H01L51/0071Polycyclic condensed heteroaromatic hydrocarbons
    • H01L51/0072Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ringsystem, e.g. phenanthroline, carbazole
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0077Coordination compounds, e.g. porphyrin
    • H01L51/0084Transition metal complexes, e.g. Ru(II)polypyridine complexes
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/42Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for sensing infra-red radiation, light, electro-magnetic radiation of shorter wavelength or corpuscular radiation and adapted for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation using organic materials as the active part, or using a combination of organic materials with other material as the active part; Multistep processes for their manufacture
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/50Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes [OLED] or polymer light emitting devices [PLED];
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies or technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/06Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1018Heterocyclic compounds
    • C09K2211/1025Heterocyclic compounds characterised by ligands

Similar Documents

Publication Publication Date Title
Seo et al. Novel D-π-A system based on zinc porphyrin dyes for dye-sensitized solar cells: synthesis, electrochemical, and photovoltaic properties
Iqbal et al. Trilateral π-conjugation extensions of phenothiazine-based dyes enhance the photovoltaic performance of the dye-sensitized solar cells
Chen et al. Dipolar compounds containing fluorene and a heteroaromatic ring as the conjugating bridge for high‐performance dye‐sensitized solar cells
Bodedla et al. Benzimidazole-branched isomeric dyes: effect of molecular constitution on photophysical, electrochemical, and photovoltaic properties
Ortiz Triarylamine-BODIPY derivatives: A promising building block as hole transporting materials for efficient perovskite solar cells
Dai et al. Synthesis of phenothiazine-based di-anchoring dyes containing fluorene linker and their photovoltaic performance
Hong et al. Performance of dye-sensitized solar cells based on novel sensitizers bearing asymmetric double D− π− A chains with arylamines as donors
Wang et al. A new thermal-stable truxene-based hole-transporting material for perovskite solar cells
Ye et al. Effect of the acceptor and alkyl length in benzotriazole-based donor-acceptor-donor type hole transport materials on the photovoltaic performance of PSCs
Guo et al. A novel asymmetric phthalocyanine-based hole transporting material for perovskite solar cells with an open-circuit voltage above 1.0 V
Cheng et al. Organic dyes containing indolodithienopyrrole unit for dye-sensitized solar cells
Wang et al. A new carbazole-based hole-transporting material with low dopant content for perovskite solar cells
Yan et al. Ethynylene-linked planar rigid organic dyes based on indeno [1, 2-b] indole for efficient dye-sensitized solar cells
Qian et al. 6H-Indolo [2, 3-b] quinoxaline-based organic dyes containing different electron-rich conjugated linkers for highly efficient dye-sensitized solar cells
Qin et al. Panchromatic donor–acceptor–acceptor sensitizers based on 4H-cyclopenta [2, 1-b: 3, 4-b′] dithiophen-4-one as a strong acceptor for dye-sensitized solar cells
Li et al. Truxene π-expanded BODIPY star-shaped molecules as acceptors for non-fullerene solar cells with over 13% efficiency
Hong et al. Synthesis of double D–A branched organic dyes employing indole and phenoxazine as donors for efficient DSSCs
Qian et al. Indeno [1, 2-b] indole-based organic dyes with different acceptor groups for dye-sensitized solar cells
Maglione et al. Tuning optical absorption in pyran derivatives for DSSC
CN102002037B (en) Triphenylamine compound and application thereof
CN111704624A (en) Indolo[3,2,1-kl]phenoxazine compound, preparation method and application thereof, and electronic device
Pan et al. Improved Conversion efficiency in dye-sensitized solar cells based on porphyrin dyes with dithieno [3, 2-b: 2′, 3′-d] pyrrole donor
Keremane et al. Simple 3, 6‐disubstituted Carbazoles as Potential Hole Transport Materials: Photophysical, Electrochemical and Theoretical Studies
Lim et al. Organic sensitizers possessing carbazole donor and indeno [1, 2-b] thiophene spacer for efficient dye sensitized solar cells
Cheng et al. D–π–A–π–A featured dyes containing different electron-withdrawing auxiliary acceptors: The impact on photovoltaic performances