JP2007280747A - Electrode material and secondary battery and capacitor using the same - Google Patents

Abstract

（式中、ｍは０または１、ｎは２〜２００の整数である。）で表される硫黄含有芳香族ポリマーにより電極材料を構成し、これを二次電池およびキャパシタの正極材料として用いる。
【選択図】なしAn electrode material made of a sulfur-containing aromatic polymer having excellent redox activity and improved theoretical capacity and conductivity, and a secondary battery and a capacitor using the same are provided.
A tetrathionaphthalene polymer having an imino bond at a linking portion is represented by the following formula (1).
[Chemical 1]

(Wherein m is 0 or 1, and n is an integer of 2 to 200). An electrode material is constituted by a sulfur-containing aromatic polymer, and this is used as a positive electrode material for secondary batteries and capacitors.
[Selection figure] None

Description

  The present invention relates to an electrode material comprising an organic sulfur compound having reversible redox activity, and a secondary battery and a capacitor using the same.

Lithium secondary batteries have high energy density and high output, so they are used in mobile devices such as mobile phones and laptop computers, and are also being considered for applications in electric vehicles. Yes.
In a conventional lithium secondary battery, a lithium-containing metal composite oxide is mainly used as a positive electrode material. However, since its capacity is limited, organic sulfur has recently been used as an alternative material. Compounds are attracting attention.

Among the organic sulfur compounds, a derivative in which a thiol group is introduced into an acene compound has a disulfide bond serving as a redox active site in the molecule, and thus is expected as an organic electrode material.
For example, in Patent Document 1, as shown in the following formula (2), 4 electrons per molecule are obtained by a redox reaction by cleavage and cyclization of two dithiol rings of tetrathionaphthalene (hereinafter abbreviated as TTN). It is described that the theoretical capacity is as large as 425 mAh / g.

However, the redox reaction of TTN has a low operating voltage and inferior charge / discharge cycle characteristics, and is not sufficient as electrode material performance.
On the other hand, as shown in the following formula (3), by imparting a positive charge to the two dithiol rings of TTN, a two-electron reaction occurs without opening the dithiol ring. Although the capacity is 213 mAh / g, which is inferior to the above case, it is recognized that an operating voltage equivalent to that of the current lithium secondary battery can be obtained (for example, see Patent Document 2).

  As described above, TTN has been considered promising as an organic sulfur cathode material having a high energy density and exhibiting redox activity. However, since it has a relatively low molecular weight, it is eluted into an electrolyte solution by repeated potential sweeps. It has drawbacks, has problems with cycle characteristics, and is difficult to use as an electrode.

特開２００１−２７３９０１号公報 国際公開第２００５／０９６４１７号パンフレット Therefore, the present inventors have studied to suppress the elution of TTN into the electrolytic solution, and as a result, by polymerizing TTN, insolubilization in the electrolytic solution can be achieved, and further, redox active sites are formed in the connecting portion. It was proposed to improve the charge / discharge capacity with respect to the monomer by imparting.
Specifically, as shown in the following formula (4), both ends of TTN are molecularly modified, and then polymerized via a thioether bond (-S-) to form a thianthrene skeleton, whereby By suppressing the elution and further providing a redox active site to the connecting portion, a three-electron reaction per monomer unit can be achieved, and the theoretical capacity and cycle characteristics can be improved.

JP 2001-273901 A International Publication No. 2005/096417 Pamphlet

  In the TTN polymer, TTNs are linked by a thioether bond, and it is expected that the performance of the electrode material will be further improved by substituting the linked part with another group having redox activity.

  That is, the present invention has been found as a result of repeated research aimed at improving electrode material performance in the polymerization of TTN, and has been found to have excellent redox activity, further increase in theoretical capacity, and improvement in conductivity. It is an object of the present invention to provide an electrode material comprising a sulfur-containing aromatic polymer and a secondary battery and a capacitor using the same.

（式中、ｍは０または１、ｎは２〜２００の整数である。）で表される硫黄含有芳香族ポリマーからなることを特徴とする。
上記のように、イミノ基を連結部としてＴＴＮをポリマー化することにより、サイクル特性および電気容量の向上のみならず、導電性の向上も図ることができる。 The electrode material according to the present invention has the following formula (1):

(Wherein, m is 0 or 1, and n is an integer of 2 to 200).
As described above, by polymerizing TTN using an imino group as a linking portion, not only cycle characteristics and electric capacity can be improved, but also conductivity can be improved.

According to the present invention, there is also provided a secondary battery characterized in that the above electrode material is used for the positive electrode, a material capable of inserting and extracting lithium is used for the negative electrode, and the electrolyte is non-aqueous. .
As described above, the electrode material according to the present invention having excellent electrochemical characteristics can be suitably used for a lithium secondary battery.

Furthermore, according to the present invention, there is provided a capacitor characterized in that the above electrode material is used for the positive electrode, a material capable of doping and dedoping cations in the electrolytic solution is used for the negative electrode, and the electrolytic solution is non-aqueous. Provided.
The electrode material according to the present invention can exhibit its excellent electrochemical characteristics not only in secondary batteries but also in capacitors.

As described above, according to the electrode material of the present invention, cycle characteristics and electric capacity can be improved as compared with TTN by polymerizing TTN using an imino group as a connecting portion. Furthermore, even when the thioether group is used as a connecting portion, the electric capacity can be further improved and the conductivity can be improved.
In addition, the electrode material according to the present invention can be suitably used not only as a positive electrode material for secondary batteries and capacitors, but also applied to electrochromic display materials, electron donor and acceptor materials as organic semiconductors, etc. Is possible.

Hereinafter, the present invention will be described in more detail.
The electrode material according to the present invention is composed of a sulfur-containing aromatic polymer represented by the above formula (1).
That is, the compound represented by the formula (1) which is an electrode material according to the present invention contains TTN which is a redox active substance in a monomer unit, and an aromatic ring is linked using imino bond as a means for polymerizing TTN, The connecting portion is a ring structure including two imino bonds at a symmetric position, or connected by one imino bond.

電極反応としては、ジスルフィド結合を含む５員環でそれぞれ１電子反応、イミノ結合による連結部を構成するＨ−フェナジン骨格で１電子反応が起きるため、モノマーユニット当たり３電子反応となると推定される。 The electrode reaction mechanism of the polymer of TTN constituting the electrode material according to the present invention is as follows. In the compound represented by the formula (1), the electrode reaction mechanism when m = 1 is shown as a representative.

As the electrode reaction, a one-electron reaction occurs in each of the five-membered rings including a disulfide bond and a one-electron reaction occurs in the H-phenazine skeleton that constitutes a connecting portion by an imino bond.

  In this way, TTN is polymerized, so that elution into the electrolyte is suppressed. In addition, electrons can be exchanged even in a cyclic connecting portion having an imino bond, and per unit of monomer than TTN1 molecule. As a result, the energy density per unit weight can be improved.

In addition, the TTN polymer constituting the electrode material according to the present invention has a thiol group (-S-) formula weight of 32 when compared with the above-described conventional TTN-linked polymer. The formula weight of the imino group (—NH—) is 15, and the formula weight (molecular weight) of the monomer unit is reduced by 34 due to the difference in the formula weight of the two bonds at the linking part.
For this reason, the theoretical capacity per monomer unit can be increased from 258 mAh / g to 289 mAh / g by reducing the molecular weight.

Furthermore, the TTN polymer according to the present invention has a structure similar to polyaniline or phenazine known as a conductive polymer having an imino group as a linking moiety, so that a similar π-conjugated electron system is formed. It is thought that it is done.
Therefore, it is possible to exhibit a conductivity close to that of a metal of 1 S / cm or more, and there is an advantage that it is possible to reduce the amount of a conductive auxiliary agent such as carbon particles added to the active material during electrode production. is doing.

The TTN polymer according to the present invention as described above can be obtained by reacting a derivative in which halogen is introduced as a substituent at positions 2, 3, 6, and 7 of TTN with an alkali amide in an organic solvent.
Specifically, for example, 2,3,6,7-tetrachloro-1,4,5,8 synthesized based on a published paper (E. Klingsberg et.al., Tetrahedron, 28, 963-965 (1972)). Using T-tetrathionaphthalene (hereinafter abbreviated as TTN-4Cl) as a raw material, as shown in the following reaction formula, by refluxing with sodium amide in an organic solvent, a polymer of TTN having an imino bond as a linking moiety (hereinafter referred to as “TTN-4Cl”) , Abbreviated as poly (TTN)).

In the polymerization reaction, the mixing ratio (molar ratio) of the reaction raw materials is preferably TTN-4Cl / sodium amide = 1/2 to 1/10.
As the organic solvent, it is preferable to use an aprotic solvent such as N, N-dimethylformamide (DMF), N, N-dimethylacetamide (DMA), N-methylpyrrolidinone (NMP), or the like.
Moreover, it is preferable that reaction temperature is 100-200 degreeC, and it can carry out in about 1-48 hours.

The poly (TTN) obtained by the above production method is obtained by applying a conductive additive such as conductive carbon particles to the powder, and further adding and mixing an appropriate amount of binder on the current collector substrate. Then, a redox active film-coated electrode can be produced by pressure molding.
The electrode can achieve a practical current density of about 0.1 to 3 mA / cm ² even in the vicinity of room temperature from the initial stage of charge and discharge.

  Examples of the conductive carbon particles used as the conductive aid include carbon black, ketjen black, acetylene black, graphite, and carbon nanotube. The addition amount of the conductive carbon fine particles is preferably about 1 to 30% by weight with respect to poly (TTN).

  In addition to the conductive carbon particles, the conductive auxiliary agent includes metals such as copper, iron, silver, nickel, palladium, gold, platinum, indium and tungsten, and metal oxides such as indium oxide and tin oxide. Metal-based conductive particles may be used.

The electrode may be composed of a composite material including a metal oxide or a metal complex in addition to poly (TTN). Thereby, the energy storage ability of both poly (TTN) and a metal oxide can be utilized.
Examples of the metal oxide include a Redox active material such as lithium cobaltate (LiCoO ₂ ), lithium nickelate (LiNiO ₂ ), lithium manganate (LiMn ₂ O ₄ ), and poly (TTN) fixed between layers. Examples thereof include vanadium pentoxide (V ₂ O ₅ ), which is a possible layered metal compound.
The metal complex may be exemplified lithium salt such as olivine-type lithium iron phosphate (LiFeO ₄₎ or the like.

  Further, in the electrode, a composite material obtained by doping poly (TTN) into an electron conductive polymer such as polythiophene may be used. Such a composite material can promote the electron transfer reaction in the electrode.

In addition, the current collector substrate that supports the electrode material needs to exhibit conductivity at least on the contact surface with the redox active film by poly (TTN). For this reason, the said board | substrate can be comprised with the metal, metal oxide, carbon, etc. which are electroconductive materials, and it is preferable that it is especially what consists of copper, carbon, gold | metal | money, aluminum, or these alloys.
The shape of the substrate is not particularly limited as long as it can form a redox active film by poly (TTN). However, a substrate having irregularities on the surface or a net-like one has a large contact area with the coating film. ,preferable.

  The redox active film covering the current collector substrate preferably has a thickness of 10 to 100 μm, and the particle diameter of each particle used in the film is preferably smaller than the film thickness.

The electrode formed as described above can be suitably used for a secondary battery in which a positive electrode is used and a material capable of inserting and extracting lithium is used for the negative electrode, and the electrolyte is a non-aqueous electrolyte.
The negative electrode can be made of a lithium alloy such as metallic lithium, lithium-aluminum, or a lithium intercalation material such as carbon. These materials are preferably used in the form of a foil from the viewpoint of reducing the weight of the battery.

In addition, as electrolyte, lithium salt such as CF ₃ SO ₃ Li, (CF ₃ SO ₂ ) ₂ NLi, (CF ₃ SO ₂ ) ₂ CLi, LiBF ₄ , LiPF ₆ , LiClO ₄ is used as a solute, which is non-aqueous. A non-aqueous electrolyte solution dissolved in a solvent can be used.
The concentration of the non-aqueous electrolyte can be appropriately determined according to the type of solute and the target level of ionic conductivity, but is about 0.1 to 3 mol / l, preferably 0.5 to 2 mol / l. It is a range.

  Examples of the non-aqueous solvent include chain carbonates, cyclic carbonates, cyclic esters, nitrile compounds, acid anhydrides, amide compounds, phosphate compounds, amine compounds, and the like. Specifically, ethylene carbonate (EC), propylene carbonate (PC), diethyl carbonate (DEC), dimethoxyethane (DME), γ-butyrolactone, N-methylpyrrolidinone, N, N′-dimethylacetamide, PC and DME And a mixture of EC and DEC, a mixture of sulfolane and tetrahydrofuran, and the like.

Furthermore, the electrolyte is preferably a gel electrolyte in which the non-aqueous electrolyte is permeated and swelled in a polymer or held in a micro-crosslinked structure of the polymer from the viewpoints of mechanical strength and leakage prevention.
Examples of the polymer include polyacrylonitrile, polymethacrylate, polymethyl methacrylate, polyvinylidene fluoride, a copolymer thereof, and a graft polymer of polyethylene and polyethylene glycol.

In addition to the secondary battery as described above, the electrode material according to the present invention is suitable for a positive electrode of a capacitor of a non-aqueous electrolyte solution using a material capable of doping and dedoping a cation in the electrolyte solution to the negative electrode. Can be used.
The electrode material can contribute to the improvement of energy density even in a capacitor.

The capacitor electrolyte includes quaternary ammonium salts such as tetramethylammonium tetrafluoroborate, tetraethylammonium hexafluorophosphate, tetrabutylammonium tetrafluoroborate, triethylmonomethylammonium tetrafluoroborate, etc. A nonaqueous electrolytic solution in which a solute is dissolved in a nonaqueous solvent is preferably used.
Moreover, as said non-aqueous solvent, ether compounds, such as ethylene glycol, propylene glycol, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, can be used individually or in mixture with another organic solvent, for example.

EXAMPLES Hereinafter, although this invention is demonstrated further more concretely based on an Example, this invention is not restrict | limited by the following Example.
(Synthesis of TTN-4Cl)
15 g of octachloronaphthalene and 6 g of sulfur were placed in a 200 ml flask and heated to 310 ° C. under a nitrogen stream. Although a large amount of sulfur dichloride was generated on the way, it was allowed to cool after being kept at 310 ° C. for about 20 minutes.
After cooling to room temperature, refluxing with carbon disulfide and washing were repeated twice.
After filtration, vacuum drying was performed to obtain TTN-4Cl with a yield of 75%.
As a result of elemental analysis of the product, C: 30.8%, H: 0.2% or less, S: 33.7%, Cl: 36.3% (weight ratio), and TTN-4Cl The values almost coincided with the theoretical values (C: 30.8%, S: 32.8%, Cl: 36.4% (weight ratio)).

(Polymerization of TTN-4Cl)
390 mg of TTN-4Cl and 156 mg of sodium amide were pulverized and mixed and put into 100 ml of DMF solvent. The reaction solution was bubbled with argon gas and replaced with inert gas.
While the bubbling was continued, the reaction solution was heated to 160 ° C. and heated to reflux for 24 hours. As a result, black powder was precipitated in the reaction solution.
The obtained black powder was repeatedly refluxed and washed with water, acetone and DMF to remove unreacted raw materials.
After filtration, vacuum drying was performed at 100 ° C. to obtain 195 mg of the target compound. Yield was about 70% assuming the product was poly (TTN).

The following various qualitative analyzes were performed on the product.
(Elemental analysis)
As a result of elemental analysis measurement of the product, C: 43.0%, H: 0.7%, N: 10.3%, S: 46.5% (weight ratio), poly (TTN) (molecular formula) : (C ₁₀ H ₂ N ₂ S ₄ ) _n ) (C: 43.2%, H: 0.72%, N: 10.1%, S: 46.0% (weight ratio)) It was almost the same.

(Infrared spectrum)
In addition, as a result of infrared spectrum measurement, the infrared spectrum of the obtained product is different from the raw material TTN-4Cl, and several relatively strong peaks are newly detected at 1100 to 1200 cm ^−1. It was done.
This is presumed to be attributable to the CN bond generated in the region of 1050 to 1250 cm ^{−1 in} the stretching vibration, and suggests that the TTN monomers are linked by the CN bond.

(Thermogravimetric analysis)
Thermogravimetric analysis was performed on TTN-4Cl, which is a raw material in polymerization, and the obtained poly (TTN).
With respect to TTN-4Cl, a rapid weight reduction was observed from around 300 ° C., but in comparison with this, the product poly (TTN) did not show a rapid weight reduction from 300 ° C.
From this, it is presumed that the product is an oligomer or polymer in which the polymerization reaction has proceeded.

  From the measurement results of the elemental analysis, infrared spectroscopic spectrum, and thermogravimetric analysis, the product was identified as poly (TTN).

  Furthermore, as for the evaluation of electrochemical characteristics, the product was measured for electric capacity by a charge / discharge test, cycle characteristics, and AC impedance measurement.

(Charge / discharge test)
70 mg of the product was dispersed using NMP as a dispersion medium, and 20 mg of carbon black powder and 10 mg of a binder polymer were added as a conductive aid to make a paste. This was applied to an aluminum foil and dried to obtain a battery positive electrode. The electrode thickness was about 30 μm.
This electrode was cut into 20 mm × 20 mm, and aluminum metal was tabbed to obtain a positive electrode.
For the battery negative electrode, metallic lithium cut to 30 mm × 30 mm was used.
As the electrolytic solution, a 1.0 M electrolytic solution was prepared by using lithium tetrafluoroborate as an electrolyte salt in a mixed solution (weight ratio 1/3) of ethylene carbonate (EC) / diethyl carbonate (DEC).

A battery was prepared using the positive electrode, the negative electrode, the electrolytic solution, and the separator, and a charge / discharge test was performed. The potential range was 3.0 to 4.3 V, and the charging and discharging current was 0.1 mA / cm ² .
The discharge capacity at that time was about 270 mAh / g, which is close to the theoretical capacity (289 mAh / g), relative to poly (TTN) as the active material.

(Cycle characteristics)
FIG. 1 shows the evaluation results of the cycle characteristics. It was confirmed that poly (TTN) exhibits good cycle characteristics with little decrease in electric capacity even when charging and discharging are repeated, as compared with TTN-4Cl which is a raw material for polymerization.

(AC impedance measurement)
Two types of poly (TTN) (thioether (-S-) linked polymer) and the product poly (TTN) (imino (-NH-) linked polymer) described in the background art were used, respectively. A battery was produced.
An AC voltage of 10 mV was applied to each battery at a voltage of 3.8 V, an AC impedance measurement was performed, and a Cole-Cole plot was analyzed to compare electrode resistance during anion doping.

FIG. 2 shows the result of the Cole-Cole plot. When each resistance component was separated and analyzed, the radius of the semicircular arc corresponding to the reaction resistance of the electrode was larger in the thioether-linked polymer electrode than in the imino-linked polymer electrode, A significant decrease in the reaction resistance of the imino-linked polymer electrode during doping (3.8 V) was observed.
This result suggests that the electroconductivity of the electrode was improved by doping the imino group linking part with an anion. That is, as with other conductive polymers (for example, polyaniline), it is considered that poly (TTN) linked by an imino group forms a π-conjugated electron system due to anion doping. It was confirmed that the conductivity was improved by connecting with NH-).

It is a graph which shows the cycle characteristic of poly (TTN) in an Example. It is a graph which shows the comparison by the difference in the connection part of the alternating current impedance measurement of poly (TTN) in an Example.

Claims (3)

Following formula (1)

(Wherein, m is 0 or 1, and n is an integer of 2 to 200).   A secondary battery characterized in that the electrode material according to claim 1 is used for the positive electrode, a material capable of inserting and extracting lithium is used for the negative electrode, and the electrolyte is non-aqueous.   A capacitor characterized in that the electrode material according to claim 1 is used for the positive electrode, a material capable of doping and dedoping cations in the electrolytic solution is used for the negative electrode, and the electrolytic solution is non-aqueous.

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