JP5863204B2 - Binder for positive electrode of lithium ion secondary battery and positive electrode material - Google Patents

Description

  The present invention relates to a binder for a positive electrode of a lithium ion secondary battery and a positive electrode material.

  In recent years, in order to meet the needs of electric vehicles, there is an urgent need to increase the output of lithium ion secondary batteries. In general, there are two important factors for increasing the output of a battery. One is that the electrode material has high electron conductivity, and the other is that lithium ion has high conductivity. When either one is inferior, the internal resistance of the battery becomes high and sufficient output characteristics cannot be obtained. The main cause of the internal resistance is the electrode material where the reaction interface between ion conduction and electron conduction is concentrated.

  In general, a positive electrode material of a lithium ion secondary battery is configured by binding a current collector and an active material with a binder. As the binder, polyvinylidene fluoride having a strong binding force is used. However, polyvinylidene fluoride does not have electronic conductivity, and a conductive additive is mixed as a countermeasure. However, the conductivity is still insufficient. Moreover, since there is no conductivity of lithium ions, it is an obstacle to high output.

  It has been proposed to use a conductive polymer compound such as polyaniline as a conductive aid for improving the conductivity of the binder (for example, Patent Document 1). However, an electrode material using polyaniline as a binder has a problem of poor electrochemical stability and insufficient storage stability and cycle characteristics. Cycle characteristics refer to the degree of deterioration of battery capacity when one cycle is discharged after charging and the cycle is repeated.

Further, LiCoO ₂ is currently widely used as a positive electrode material for lithium ion secondary batteries, but it is problematic from the viewpoint of safety because it decomposes while generating heat from around 160 ° C. Therefore, replacement with LiFePO ₄ having higher safety without causing exothermic decomposition even at high temperatures is being studied.
However, LiFePO ₄ is poor in electron conductivity, and has a problem that the cycle characteristics are severely deteriorated particularly when charging and discharging at high speed. Measures such as coating an active material with carbon in order to supplement conductivity are taken (for example, Patent Document 2), but the cost is high and productivity is inferior, which hinders practical use.

JP 2007-52940 A JP 2006-302671 A

  The present invention has been made in view of the above problems, and an object of the present invention is for an electrode that can increase the output of a lithium ion secondary battery and has little battery capacity deterioration even when high-speed charge / discharge is repeated. It is to provide a binder and an electrode material.

［式中、ＯＲ ¹ 及びＯＲ ⁴ はそれぞれ独立にオキシエチレン基、オキシプロピレン基又はオキシブチレン基を表し、Ｒ ² 及びＲ ⁵ はそれぞれ独立に炭素数１〜１２の直鎖又は分岐のアルキル基を表し、Ｒ ³ は炭素数１〜４の直鎖又は分岐のアルキレン基を表し、ｎ及びｍはそれぞれ独立に０〜５の整数である。］
［３］
前記チオフェン繰り返し単位（α１）が、一般式（１）におけるＯＲ ¹ がオキシエチレン基であり、ｎが０の場合にはＲ ² が炭素数３〜１２の直鎖又は分岐のアルキル基であり、ｎが１以上の場合にはＲ ² が炭素数１〜６の直鎖又は分岐のアルキル基であるものであり、前記チオフェン繰り返し単位（α２）が、一般式（２）におけるＲ ³ が炭素数１〜３のアルキレン基であって、ＯＲ ⁴ がオキシエチレン基であり、ｍが０の場合にはＲ ⁵ が炭素数３〜１２の直鎖又は分岐のアルキル基であり、ｍが１以上の場合にはＲ ⁵ が炭素数１〜６の直鎖又は分岐のアルキル基であるものである［２］記載の結着剤。
［４］
前記置換ポリチオフェン（Ｐ）における前記チオフェン繰り返し単位（α）の含有量が、置換ポリチオフェン（Ｐ）中、５０〜１００モル％である［１］〜［３］のいずれか記載の結着剤。
［５］
前記置換ポリチオフェン（Ｐ）中のヘッドｔｏテール−ヘッドｔｏテール結合の百分率で定義される立体規則性が、９０％以上である［１］〜［４］のいずれか記載の結着剤。
［６］
前記置換ポリチオフェン（Ｐ）が、前記チオフェン繰り返し単位（α１）と一般式（３）で表されるチオフェン繰り返し単位（β１）とを有する置換ポリチオフェン（Ｐ２１）、又は前記チオフェン繰り返し単位（α２）と一般式（４）で表されるチオフェン繰り返し単位（β２）とを有する置換ポリチオフェン（Ｐ２２）である［１］〜［４］のいずれか記載の結着剤。

［式中、ＯＲ ¹ 及びＯＲ ⁴ はそれぞれ独立にオキシエチレン基又はオキシプロピレン基を表し、Ｒ ² 及びＲ ⁵ はそれぞれ独立に炭素数１〜１２の直鎖又は分岐のアルキル基を表し、Ｒ ³ は炭素数１〜４の直鎖又は分岐のアルキレン基を表し、Ｍ ⁺ はアルカリ金属カチオン又はプロトンを表し、ｎ及びｍはそれぞれ独立に０〜５の整数である。］
［７］
［１］〜［６］のいずれか記載の結着剤によって、活物質（Ｂ）を集電体（Ｃ）に結着してなるリチウムイオン二次電池用正極材料。
［８］
前記活物質（Ｂ）が、リチウム遷移金属複合酸化物である［７］記載の正極材料。
The inventors of the present invention have reached the present invention as a result of studies to achieve the above object. That is, the present invention
At least some of the thiophene repeat units are
(A) a polyether group having 1 to 9 repeating units composed of an oxyalkylene group having 2 to 4 carbon atoms, one end of which is an alkoxy group having 1 to 15 carbon atoms,
(B) an alkoxy group,
(C) an alkoxyalkyl group or (d) a substituted polythiophene (α) that is a thiophene repeating unit (α) substituted at the 3-position and / or 4-position of the thiophene ring by an alkyl group substituted with the polyether group (a) Lithium ion secondary battery positive electrode binder (A) characterized by containing P); and lithium formed by binding the active material (B) to the current collector (C) by the binder It is a positive electrode material for an ion secondary battery.
The basic features and various aspects of the present invention are listed below.
[1]
At least some of the thiophene repeat units are
(A) a polyether group having 1 to 9 repeating units composed of an oxyalkylene group having 2 to 4 carbon atoms, one end of which is an alkoxy group having 1 to 15 carbon atoms,
(B) an alkoxy group,
(C) an alkoxyalkyl group or
(D) containing a substituted polythiophene (P) which is a thiophene repeating unit (α) substituted at the 3-position and / or 4-position of the thiophene ring by an alkyl group substituted with the polyether group (a). A binder for a positive electrode of a lithium ion secondary battery (A).
[2]
The thiophene repeating unit (α) is the thiophene repeating unit (α1) represented by the general formula (1) and / or the thiophene repeating unit (α2) represented by the general formula (2). Dressing.

[ Wherein , OR ¹ and OR ⁴ each independently represents an oxyethylene group, an oxypropylene group or an oxybutylene group, and R ² and R ⁵ each independently represents a linear or branched alkyl group having 1 to 12 carbon atoms. R ³ represents a linear or branched alkylene group having 1 to 4 carbon atoms, and n and m are each independently an integer of 0 to 5. ]
[3]
In the thiophene repeating unit (α1), OR ¹ in the general formula (1) is an oxyethylene group, and when n is 0, R ² is a linear or branched alkyl group having 3 to 12 carbon atoms, when n is 1 or more are those wherein R ² is a linear or branched alkyl group having 1 to 6 carbon atoms, wherein the thiophene repeating unit ([alpha] 2) is, R ³ carbon atoms in the general formula (2) 1 to 3 alkylene groups, OR ⁴ is an oxyethylene group, and when m is 0, R ⁵ is a linear or branched alkyl group having 3 to 12 carbon atoms, and m is 1 or more. In some cases, the binder according to [2], wherein R ⁵ is a linear or branched alkyl group having 1 to 6 carbon atoms.
[4]
The binder according to any one of [1] to [3], wherein a content of the thiophene repeating unit (α) in the substituted polythiophene (P) is 50 to 100 mol% in the substituted polythiophene (P).
[5]
The binder according to any one of [1] to [4], wherein the stereoregularity defined by the percentage of head-to-tail-head-to-tail bonds in the substituted polythiophene (P) is 90% or more.
[6]
The substituted polythiophene (P) is a substituted polythiophene (P21) having the thiophene repeating unit (α1) and the thiophene repeating unit (β1) represented by the general formula (3), or the thiophene repeating unit (α2) and the general The binder according to any one of [1] to [4], which is a substituted polythiophene (P22) having a thiophene repeating unit (β2) represented by the formula (4).

[ Wherein , OR ¹ and OR ⁴ each independently represent an oxyethylene group or an oxypropylene group, R ² and R ⁵ each independently represent a linear or branched alkyl group having 1 to 12 carbon atoms, R ³ Represents a linear or branched alkylene group having 1 to 4 carbon atoms, M ⁺ represents an alkali metal cation or a proton, and n and m are each independently an integer of 0 to 5. ]
[7]
A positive electrode material for a lithium ion secondary battery obtained by binding the active material (B) to the current collector (C) with the binder according to any one of [1] to [6].
[8]
The positive electrode material according to [7], wherein the active material (B) is a lithium transition metal composite oxide.

  The binder for the positive electrode of the lithium ion secondary battery of the present invention has the effects of greatly improving the output characteristics of the battery and further greatly improving the cycle characteristics during high-speed charging.

The binder (A) for a lithium ion secondary battery positive electrode of the present invention comprises 1 to 9 repeating units in which at least a part of the thiophene repeating units is (a) an oxyalkylene group having 2 to 4 carbon atoms. A polyether group whose one end is an alkoxy group having 1 to 15 carbon atoms, (b) an alkoxy group, (c) an alkoxyalkyl group, or (d) an alkyl group substituted with the polyether group (a). And substituted polythiophene (P) which is a thiophene repeating unit (α) substituted at the 3-position and / or 4-position of the thiophene ring (also referred to as “thiophene repeating unit (α)” in the present specification).
In addition, each element enumerated with the symbols (a), (b), (c) and (d) is referred to as a polyether group (a), an alkoxy group (b), Also referred to as an alkoxyalkyl group (c) and an alkyl group (d) substituted with the polyether group (a).

The binder (A) for a lithium ion secondary battery positive electrode according to the present invention has conventionally been obtained by using a substituted polythiophene (P) having both electron conductivity and lithium ion conductivity as an essential component. Electron conduction that has been performed through the contact point can be performed throughout the binder.
Further, the positive electrode binder (A) of the present invention comprises a polyether group (a), an alkoxy group (b), an alkoxyalkyl group (c) and an alkyl group (d) substituted with the polyether group (a). ) Substituted thiophene repeating unit (α), the lithium ion conductivity is improved compared to conventional binders, and as a result, the internal resistance and electrical resistance are greatly improved, resulting in output Improved characteristics and cycle characteristics during high speed charge / discharge.

As said polyether group (a), it has a repeating unit consisting of a C2-C4 oxyalkylene group, the repeating unit number is 1-9, and one terminal is a C1-C15 alkoxy group. Some polyether groups are mentioned.
Examples of the oxyalkylene group having 2 to 4 carbon atoms include an oxyethylene group, an oxypropylene group, and oxybutylene.

  Examples of the terminal alkoxy group having 1 to 15 carbon atoms include methoxy group, ethoxy group, propoxy group, isopropoxy group, n-, iso-, sec- or tert-butoxy group, pentyloxy group, hexyloxy group, heptyloxy Group, octyloxy group, 2-ethylhexyloxy group, nonyloxy group, decyloxy group, undecyloxy group, dodecyloxy group, tridecyloxy group, tetradecyloxy group and pentadecyloxy group.

  As said alkoxy group (b), the C1-C15 alkoxy group similar to what was illustrated by the said polyether group (a) is mentioned.

As said alkoxyalkyl group (c), the C1-C4 alkyl group substituted by the C1-C15 alkoxy group is mentioned.
Examples of the alkoxy group having 1 to 15 carbon atoms include those exemplified in the polyether group (a). Examples of the alkyl group having 1 to 4 carbon atoms include a methyl group, an ethyl group, n- or Examples thereof include an iso-propyl group and an n-, sec-, iso- or tert-butyl group.

  Examples of the alkyl group in the alkyl group (d) substituted with the polyether group (a) of the thiophene repeating unit (α) include a methyl group, an ethyl group, an n- or iso-propyl group, and n-, sec-, Examples include iso- or tert-butyl group.

  The substituted polythiophene (P) in the present invention is preferably represented by the thiophene repeating unit (α1) and / or the general formula (2) represented by the following general formula (1) from the viewpoint of conductivity and solvent solubility. The substituted polythiophene (P1) having a thiophene repeating unit (α2). The substituted polythiophene (P1) becomes soluble in a solvent by having the thiophene repeating unit (α1) or (α2).

OR ¹ and OR ⁴ in the general formula (1) or (2) each independently represent an oxyethylene group, an oxypropylene group or an oxybutylene group, and an oxyethylene group is preferred from the viewpoint of conductivity.

R ² and R ⁵ in the general formula (1) or (2) are each independently a linear or branched alkyl group having 1 to 12 carbon atoms (for example, methyl group, n- or iso-propyl group, n- , Iso-, sec- or tert-butyl group, n- or iso-pentyl group, cyclopentyl group, n- or iso-hexyl group, cyclohexyl group, n- or iso-heptyl group, n- or iso-octyl group, 2-ethylhexyl group, n- or iso-nonyl group, n- or iso-decyl group, n- or iso-undecyl group and n- or iso-dodecyl group).

When n described later is 1 or more, R ² is preferably a linear or branched alkyl group having 1 to 6 carbon atoms, more preferably a linear or branched chain having 1 to 4 carbon atoms, from the viewpoint of conductivity. It is an alkyl group.
When n is 0, R ² is preferably a linear or branched alkyl group having 3 to 12 carbon atoms, more preferably a linear or branched alkyl group having 6 to 12 carbon atoms, from the viewpoint of conductivity. It is.

When m described later is 1 or more, R ⁵ is preferably a linear or branched alkyl group having 1 to 6 carbon atoms, more preferably a linear or branched group having 1 to 4 carbon atoms, from the viewpoint of conductivity. It is an alkyl group.
When m is 0, R ⁵ is preferably a linear or branched alkyl group having 3 to 12 carbon atoms, more preferably a linear or branched alkyl group having 6 to 12 carbon atoms, from the viewpoint of conductivity. It is.

R ³ in the general formula (2) is a linear or branched alkylene group having 1 to 4 carbon atoms (for example, a methylene group, 1,2- or 1,3-propylene group, and 1,2-, 1,3- , 2,3- or 1,4-butylene group), preferably from the viewpoint of solvent solubility and conductivity, a linear or branched alkylene group having 1 to 3 carbon atoms, more preferably a carbon number. 1 or 2 alkylene group.

  N and m in the general formula (1) or (2) are each independently an integer of 0 to 5. n is preferably 1 to 5 and more preferably 2 to 5 from the viewpoints of solvent solubility and conductivity. m is preferably 0 to 4 and more preferably 0 to 3 from the viewpoints of solvent solubility and conductivity.

  The substituted polythiophene (P) in the present invention may consist of only the thiophene repeating unit (α) or may contain an unsubstituted thiophene repeating unit.

  The content of the thiophene repeating unit (α) in the substituted polythiophene (P) is preferably 50 to 100 mol%, more preferably 60 to 100 mol%, particularly preferably 70 to 100 mol, from the viewpoint of solvent solubility. %.

  The substituted polythiophene (P) in the present invention can be synthesized by a known method such as anionic polymerization or oxidation polymerization of a monomer corresponding to each thiophene repeating unit.

  As the monomer corresponding to the substituted thiophene repeating unit (α), the 3-position and / or 4-position of the thiophene ring is a polyether group (a), an alkoxy group (b), an alkoxyalkyl group (c) or the polyether. Examples include thiophene substituted with an alkyl group (d) substituted with the group (a) and substituted with a halogen atom at the 2nd and 5th positions.

  Specific examples of the monomer in which the 3-position of the thiophene ring is substituted with a polyether group (a) include 3- (1,3-dioxopentyl) thiophene and 3- (1,4,7-trioxaoctyl) thiophene. 3- (1,4,7,10-tetraoxaundecyl) thiophene, 3- (1,4,7,10,13-pentaoxahexadecyl) thiophene, 3- (1,4,7,10, 13,16-hexaoxypentadecyl) thiophene, 3- (1,5-dioxahexyl) thiophene, 3- (1,5,9-trioxadecyl) thiophene, 3- (1,5,9,13- Tetraoxatetradecyl) thiophene, 3- (1,4-dioxahexyl) thiophene, 3- (1,4,7-trioxanonyl) thiophene or 3- (1,4,7,10-tetraoxadodecyl) 2-position and 5-position of the thiophene and the like thiophene substituted with a halogen atom.

  Specific examples of the monomer in which the 3-position of the thiophene ring is substituted with an alkoxy group (b) include 3-methoxythiophene, 3-ethoxythiophene, 3-butoxythiophene, 3-pentyloxythiophene, 3-hexyloxythiophene, 3 -Heptyloxythiophene, 3-octyloxythiophene, 3-nonyloxythiophene, 3-decyloxythiophene, 3-undecyloxythiophene, thiophene in which 2- and 5-positions of 3-dodecyloxythiophene are substituted with halogen atoms, etc. Is mentioned.

  Specific examples of the monomer substituted with the alkoxyalkyl group (c) include 3- (2-oxapropyl) thiophene, 3- (2-oxabutyl) thiophene, 3- (2-oxapentyl) thiophene, 3- (2 -Oxahexyl) thiophene, 3- (2-oxaheptyl) thiophene, 3- (2-oxaoctyl) thiophene, 3- (2-oxanonyl) thiophene, 3- (2-oxadecyl) thiophene, 3- (2-oxaundecyl) ) Thiophene, 3- (2-oxadodecyl) thiophene, 3- (2-oxatridecyl) thiophene, 3- (2-oxatetradecyl) thiophene, 3- (2-oxapentadecyl) thiophene, 3- (2 -Oxahexadecyl) thiophene, 3- (2-oxaheptadecyl) thiophene, 3- (3-oxono Le) thiophene, 3- (4-oxodecyl) thiophene or 3- (5-hexadodecyl) thiophene and the like.

  Specific examples of the monomer substituted with the alkyl group (d) substituted with the polyether group (a) include 3- (2,5-dioxahexyl) thiophene and 3- (2,5-dioxaheptyl). ) Thiophene, 3- (2,5,8-trioxanonyl) thiophene or thiophene in which 2- and 5-positions of 3- (2,5,8-trioxadecyl) thiophene are substituted with halogen atoms. .

  Examples of the monomer corresponding to the unsubstituted thiophene repeating unit include thiophene.

  The stereoregularity (RR) of the substituted polythiophene (P) in the present invention is usually 50% or more, preferably 80% or more, more preferably 90% or more from the viewpoint of conductivity.

The definition of stereoregularity (RR) in the present invention will be described below.
As shown in the following general formulas B1 to B4, the substituted polythiophene (P) has HT-HT bond (B1), TT-HT bond (B2), HT-HH bond (B3), and TT-HH bond. There are four types (B4). Here, HT is an abbreviation for head to tail, TT is an abbreviation for tail to tail, and HH is an abbreviation for head to head.

  R in the chemical formulas of the four bond types represents a polyether group (a), an alkoxy group (b), an alkoxyalkyl group (c), or an alkyl group (d) substituted with the polyether group (a). .

The stereoregularity (RR) in the present invention is defined by the ratio (%) of HT-HT bonds (head-to-tail-head-to-tail bonds) in the substituted polythiophene (P), and is calculated by the following formula (1). .
Stereoregularity (RR) = B1 × 100 / (B1 + B2 + B3 + B4) (1)
Where B1: HT-HT bond number, B2: TT-HT bond number, B3: HT-HH bond number, B4: TT-HH bond number.

Specifically, the protons that these bonds have have specific chemical shifts (δ) by nuclear magnetic resonance ( ¹ H-NMR), so they are calculated from the integrated values of chemical shifts corresponding to the four types of bonds. can do.
In the case of the substituted polythiophene having the thiophene repeating unit (α1) represented by the general formula (1), specifically, B1: δ = 6.98, B2: δ = 7.00, B3: δ = 7.02 , B4: δ = 7.05. Therefore, the integral values S1, S2, S3, S4 in the chemical shifts unique to B1, B2, B3, B4 are calculated, and the stereoregulation rule is calculated from the ratio (%) of the integral value S1 in the chemical shift unique to B1 to the sum of the integral values. The property (RR) is calculated using the following mathematical formula (2).
Stereoregularity (RR) = S1 × 100 / (S1 + S2 + S3 + S4) (2)

  As described above, the substituted polythiophene (P) becomes soluble in the solvent when it has the thiophene repeating unit (α1) or (α2), but is further dispersed in water by introducing a structural unit having an ionic hydrophilic group. Sex substituted polythiophene (P2). Preferred as such a substituted polythiophene is a substituted polythiophene (P21) having a thiophene repeating unit (α1) and a thiophene repeating unit (β1) represented by the general formula (3), and a thiophene repeating unit (α2) And substituted polythiophene (P22) having a thiophene repeating unit (β2) represented by the formula (4).

OR ^1, R ² and n in the general formula (3) is the same as OR ^1, R ² and n in formula respectively (1). Further, R ³ in the general formula ^{(4), OR 4, R} 5 is and ^{m, R 3, OR 4, R} 5 are the same as and m in each of the general formula (2).
M ⁺ in the general formulas (3) and (4) represents an alkali metal cation (such as a lithium ion, a sodium ion, or a potassium ion) or a proton.
M ⁺ is preferably an alkali metal cation from the viewpoint of dispersibility in water, and more preferably lithium ion from the viewpoint of stability to the electrolyte.

The substituted polythiophene (P21) having the thiophene repeating unit (α1) and the thiophene repeating unit (β1) is obtained by sulfonating the substituted polythiophene (P11) having only the thiophene repeating unit (α1) as the substituted thiophene repeating unit. Can be manufactured.
The substituted polythiophene (P22) having a thiophene repeating unit (α2) and a thiophene repeating unit (β2) is a sulfonation reagent obtained by replacing the substituted polythiophene (P12) having only the thiophene repeating unit (α2) as a substituted thiophene repeating unit. Can be produced by sulfonation.
Examples of the sulfonation reagent include, but are not limited to, monochlorosulfuric acid, fuming sulfuric acid, and concentrated sulfuric acid.

The content of the thiophene repeating unit (β1) in the substituted polythiophene (P21) is usually 5 to 70 mol%, preferably 30 to 60 mol%, from the viewpoints of water dispersibility, conductivity, and ease of synthesis. More preferably, it is 50-60 mol%.
The content of the thiophene repeating unit (α1) in the substituted polythiophene (P21) is usually 30 to 95 mol%, preferably 40 to 70 mol%, more preferably from the viewpoints of water dispersibility, conductivity, and ease of synthesis. Is 40 to 50 mol%.
The contents of the thiophene repeating units (β2) and (α2) in the substituted polythiophene (P22) are the same as the contents of the thiophene repeating units (β1) and (α1) in (P21), respectively. It is the same.

  As the substituted polythiophene (P) in the present invention, the substituted polythiophene (P11) or (P12) is preferable from the viewpoint of conductivity, and the substituted polythiophene (P21) is preferable from the viewpoint of environmental load that does not use an organic solvent. ) Or (P22).

The binder (A) in the present invention may be mixed with a polymer compound or a conductive aid that assists the binding force as necessary.
When using a polymer compound that assists the binding force when the substituted polythiophene (P) is dissolved in an organic solvent to be described later, a polymer compound that is soluble in the organic solvent can be mixed. When polythiophene (P) is used by dispersing in water, a water-soluble polymer compound can be mixed.

Examples of the polymer compound soluble in the organic solvent include polyethylene, polypropylene, polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF), tetrafluoroethylene-hexafluoroethylene copolymer, tetrafluoroethylene-hexafluoropropylene. Copolymer (FEP), tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (PFA), vinylidene fluoride-hexafluoropropylene copolymer, vinylidene fluoride-chlorotrifluoroethylene copolymer, ethylene-tetrafluoroethylene Copolymer (ETFE resin), polychlorotrifluoroethylene (PCTFE), vinylidene fluoride-pentafluoropropylene copolymer, propylene-tetrafluoroethylene copolymer, ethylene - chlorotrifluoroethylene copolymer (ECTFE), vinylidene fluoride - hexafluoropropylene - tetrafluoroethylene copolymer, vinylidene fluoride - can be exemplified tetrafluoroethylene copolymer - perfluoromethyl vinyl ether.
Among these, polyvinylidene fluoride (PVDF) and polytetrafluoroethylene (PTFE) are particularly preferable.

  Examples of the water-soluble polymer compound include carboxymethyl celluloses, poly (meth) acrylic acids, polyvinyl alcohol, polyvinyl sulfonic acid, polyvinylidene fluoride, polyvinyl pyrrolidone, polyethylene oxide, polyacrylamide, poly-N-isopropylacrylamide, poly -N, N-dimethylacrylamide, polyoxyethylene, polyerylenimine and the like.

In particular, carboxymethyl celluloses include carboxymethyl cellulose (including Li salt, Na salt, K salt or NH ₄ salt), methyl cellulose, ethyl cellulose, hydroxymethyl cellulose, hydroxyethyl cellulose, cellulose acetate petrate, oxidized starch, and phosphorylated starch. .
Poly (meth) acrylic acids include (meth) acrylic acid homopolymers, copolymers of (meth) acrylic acid and itaconic acid and / or maleic acid, and their Li salts, Na salts, K Salt or NH ₄ salt.
Among these, preferred are celluloses, more preferred are carboxymethylcelluloses, and particularly preferred is carboxymethylcellulose.

  Content of the high molecular compound which assists the binding force in a binder (A) is 0 to 80 weight% normally, Preferably it is 1 to 50 weight%. If the content of the polymer compound is too large, the output is reduced, which is not preferable.

The conductive auxiliary agent that can be mixed with the binder (A) of the present invention is not particularly limited as long as it is an electron conductive material that does not cause a chemical change at the charge / discharge potential of the positive electrode material used.
Examples of the conductive assistant include graphites such as natural graphite (flaky graphite etc.) and artificial graphite, carbon blacks such as acetylene black, ketjen black, channel black, furnace black, lamp black and thermal black, carbon fiber And conductive fibers such as metal fibers, metal powders such as carbon fluoride, copper, nickel, aluminum and silver, conductive whiskers such as zinc oxide and potassium titanate, conductive metal oxides such as titanium oxide, Examples thereof include organic conductive materials such as polyphenylene derivatives, and mixtures thereof. Of these conductive agents, artificial graphite, acetylene black and nickel powder are particularly preferred.

  Although content of the conductive support agent in a binder (A) is not specifically limited, 1 to 50 weight% is preferable, More preferably, it is 1 to 30 weight%. In the case of carbon or graphite, 2 to 15% by weight is particularly preferable.

  The positive electrode material of the present invention can be obtained by kneading the binder (A), active material (B), and solvent, and then drying the kneaded product.

Specifically, the binder (A) and the active material (B) are mixed at a desired ratio, and a solvent is added thereto to obtain a slurry-like kneaded product. The obtained kneaded material is applied to a current collector such as an aluminum foil and dried, and further pressed at a predetermined pressure as necessary to obtain an electrode material.
In addition, it is preferable that the drying temperature at the time of drying a kneaded material shall be 100-150 degreeC, and it is still more preferable to set it as 120-140 degreeC. When the drying temperature is less than 100 ° C., the amount of the solvent remaining in the electrode material may increase, which may adversely affect the characteristics of the battery. On the other hand, when the temperature exceeds 150 ° C., the binder is likely to be decomposed (carbonized), which may adversely affect the characteristics of the battery.

The active material (B), can be used lithium-transition metal composite oxide, for _{example, Li x FePO 4, Li x} CoO 2, Li x NiO 2, Li x MnO 2, Li x Co y Ni 1-y O ₂ , Li _x Co _y M _1-y O _z , Li _x Ni _{1- y My} O _z , Li _x Mn ₂ O ₄ , Li _x Mn _{2- y My} O ₄ (where M is Na, Mg, Sc, Y, Mn, Fe, Co, Ni, Cu, Zn, Al, Cr, Pb, Sb and B. At least one atom selected from x, x is a number from 0 to 1.2, y is 0 to 0 0.9, and z is a number from 2.0 to 2.3).
Here, the value of x described above is a value before the start of charge / discharge, and increases or decreases due to charge / discharge. Among these, preferably Li _x FePO _4, or Li _x CoO ₂ in terms of cost, further Li _x FePO ₄ are preferable in view of safety of not exothermic decomposition even at a high temperature of over 160 degrees.

  The amount of the binder (A) relative to the active material (B) in the present invention is usually 1 to 20% by weight, preferably 3 to 10% by weight, and more preferably 3 to 5% by weight. If the amount of the binder is too small, the active material cannot be sufficiently bonded, and if the amount is too large, the energy density of the battery is lowered, which is not preferable.

  In the solvent for kneading the binder (A) and active material (B) of the present invention, the substituted polythiophene (P) contained in the binder (A) is substituted polythiophene (P11) or (P12). In some cases, an organic solvent having a boiling point of less than 150 ° C. is preferred, and in the case of substituted polythiophene (P21) or (P22), water is preferred.

  The organic solvent preferably has a boiling point of less than 150 ° C. If the boiling point is 150 ° C. or higher, the amount of the solvent remaining in the electrode material in the drying process may increase, which may adversely affect the battery characteristics. Examples of such an organic solvent include 1-methyl-2-pyrrolidone, dimethylformamide, chloroform, tetrahydrofuran (hereinafter abbreviated as THF), 1,3-dioxolane, 1,4-dioxane, toluene and the like. Among these, 1-methyl-2-pyrrolidone and 1,3-dioxolane are preferable from the viewpoint of solubility of the substituted polythiophene (P).

  The amount of the solvent when producing the positive electrode material of the present invention is 50 to 300% by weight, preferably 50 to 100% by weight, based on the active material (B). If the amount of the solvent is too small, the active material (B) and the binder (A) cannot be sufficiently kneaded, and if the amount is too large, the amount of the solvent remaining in the electrode material may increase, which may contribute to battery characteristics. Since it may have an adverse effect, it is not preferable.

The current collector used in the present invention is not particularly limited as long as it is an electronic conductor that does not cause a chemical change in the charge / discharge potential of the positive electrode material to be used. For example, the material is stainless steel, aluminum, titanium, carbon, and conductive. In addition to the functional resin, the surface of aluminum or stainless steel treated with carbon or titanium is used. Of these, aluminum and aluminum alloys are particularly preferable. These materials can be used by oxidizing the surface thereof. Further, it is desirable to make the current collector surface uneven by surface treatment.
Examples of the shape of the current collector include films, sheets, nets, punched materials, lath bodies, porous bodies, foams, fiber groups, nonwoven fabric molded bodies, and the like.
The thickness of the current collector is not particularly limited, but is preferably 1 to 500 μm.

  Hereinafter, although an example and a comparative example explain the present invention further, the present invention is not limited to these. Hereinafter, a part shows a weight part.

<Production Example 1>
Synthesis of poly (3-octyloxythiophene) (P-1):
(1) Synthesis of 3-octyloxythiophene;
1.25 parts of sodium hydride was dispersed in 25 parts of N, N-dimethylformamide, and 17.65 parts of octanol was added dropwise thereto. The reaction solution foamed and became cloudy. When the foaming stopped, 5 parts of 3-bromothiophene (manufactured by Aldrich) and 0.445 parts of copper (I) bromide were sequentially added to the reaction solution.
The reaction solution was heated to 110 ° C. and reacted for 1 hour. After completion of the reaction, the mixture was allowed to cool to room temperature, 30 parts of 1M aqueous ammonium chloride solution was added, and the mixture was transferred to a separatory funnel using 30 parts of ethyl acetate, and then the aqueous layer was separated. Further, the organic layer was washed twice with 30 parts of distilled water, and then ethyl acetate was distilled off to obtain 6 parts of 3-octyloxythiophene (yield 97%).

(2) Synthesis of 2,5-dibromo-3-octyloxythiophene;
6 parts of the above 3-octyloxythiophene and 13.96 parts of N-bromosuccinimide were dissolved in THF and reacted at room temperature for 2 hours.
The precipitate was removed with a glass filter using 50 parts of ethyl acetate, and THF and ethyl acetate were distilled off. The obtained mixture was purified by a silica gel column to obtain 8.41 parts (yield 78.7%) of 2,5-dibromo-3-octyloxythiophene.

(3) Synthesis of poly (3-octyloxythiophene) (P-1);
After dissolving 8.41 parts of the above 2,5-dibromo-3-octyloxythiophene in 30 parts of THF, 25 parts of methylmagnesium bromide THF solution was added and reacted at 75 ° C. for 30 minutes. To the reaction solution, 0.127 part of [1,3-bis (diphenylphosphino) propane] -dichloronickel (II) was added, and the reaction was further continued for 2 hours at 75 ° C.
The reaction solution was allowed to cool to room temperature, and 5 parts of methanol was added. The reaction mixture was transferred to a Soxhlet extractor and washed sequentially with 150 parts of methanol and 150 parts of hexane. Finally, the residue was extracted with 150 parts of chloroform, and the solvent was distilled off to obtain 2.95 parts of poly (3-octyloxythiophene) (P-1) (63% yield, 48% overall yield). . The stereoregularity calculated by the above-mentioned method using ¹ H-NMR was 96.3%.

<Production Example 2>
Synthesis of poly (3-decyloxythiophene) (P-2):
Poly (3-deca) having a stereoregularity of 95.6% as in Production Example 1 except that 21.45 parts of decanol (manufactured by Tokyo Chemical Industry Co., Ltd.) was used instead of 17.65 parts of octanol. Noxythiophene) (P-2) (3.05 parts) was obtained (total yield: 41.7%).
When changing octanol to decanol, the operation was carried out by adjusting the amount of each raw material so that the molar ratio of the reaction components and the weight ratio of the non-reaction components (solvent, etc.) were the same as in Production Example 1. went. It carried out similarly about the following manufacture examples 3, 4, 6-9, and 11.

<Production Example 3>
Synthesis of poly (3-dodecyloxythiophene) (P-3):
Poly (3-dodecyl) having a stereoregularity of 96.6% as in Production Example 1 except that 25.26 parts of dodecanol (manufactured by Tokyo Chemical Industry Co., Ltd.) was used instead of 17.65 parts of octanol. Oxythiophene) (P-3) 3.51 parts were obtained (42.9% overall yield).

<Production Example 4>
Synthesis of poly {3- (1,4-dioxahexadecyl) thiophene} (P-4):
The stereoregularity is 96.4% in the same manner as in Production Example 1 except that 31.23 parts of ethylene glycol monododecyl ether (manufactured by Tokyo Chemical Industry Co., Ltd.) is used instead of 17.65 parts of octanol. P-4) 4.27 parts were obtained (44.8% overall yield).

<Production Example 5>
Synthesis of poly {3- (2,5-dioxaheptyl) thiophene} (P-5):
(1) Synthesis of 3-bromomethylthiophene;
3-methylthiophene [Tokyo Chemical Industry Co., Ltd.] 5 parts (50.9 mmol), N-bromosuccinimide 9.97 parts (56.0 mmol), dibenzoyl peroxide [Tokyo Chemical Industry Co., Ltd.] 0. After 12 parts (0.50 mmol) was dissolved in 30 parts of benzene, the temperature was raised to 100 ° C. and reacted for 4 hours. After completion of the reaction, the mixture was allowed to cool to room temperature, 30 parts of 1M aqueous sodium thiosulfate solution was added, and the mixture was transferred to a separatory funnel, and then the aqueous layer was separated. Further, the organic layer was washed twice with 30 parts of distilled water, and then benzene was distilled off to obtain 6.32 parts (35.7 mmol) of 3-bromomethylthiophene (yield 70.1%).

(2) Synthesis of 3- (2,5-dioxaheptyl) thiophene;
3.54 parts (39.3 mmol) of 2-ethoxyethanol was dissolved in 15 parts of THF, and sodium hydride (60% paraffin dispersion) was added thereto. 6.32 parts (35.7 mmol) of the above 3-bromomethylthiophene was dissolved in 15 parts of THF, added dropwise over 2 hours, then heated to 100 ° C. and reacted for 4 hours. After completion of the reaction, the mixture was allowed to cool to room temperature, 30 parts of distilled water was added, and the mixture was transferred to a separatory funnel, and the aqueous layer was separated. Further, the organic layer was washed twice with 30 parts of distilled water, THF was distilled off, and the resulting mixture was purified with a silica gel column to obtain 5.68 parts of 3- (2,5-dioxaheptyl) thiophene. (30.5 mmol) (yield 85.4%) was obtained.

(3) Synthesis of 2,5-dibromo-3- (2,5-dioxaheptyl) thiophene;
5.68 parts (30.5 mmol) of 3- (2,5-dioxaheptyl) thiophene and 11.9 parts (67.1 mmol) of N-bromosuccinimide were dissolved in THF and reacted at room temperature for 2 hours. .
The precipitate was removed with a glass filter using 50 parts of ethyl acetate, and THF and ethyl acetate were distilled off. The obtained mixture was purified with a silica gel column to obtain 8.11 parts (23.6 mmol) of 2,5-dibromo-3- (2,5-dioxaheptyl) thiophene (yield 77.3%). It was.

(4) Synthesis of poly {3- (2,5-dioxaheptyl) thiophene} (P-5);
After dissolving 8.11 parts (23.6 mmol) of the above 2,5-dibromo-3- (2,5-dioxaheptyl) thiophene in 30 parts of THF, 25 parts of methylmagnesium bromide THF solution was added, and the mixture was heated at 75 ° C. The reaction was performed for 30 minutes. To the reaction solution, 0.127 part of [1,3-bis (diphenylphosphino) propane] -dichloronickel (II) was added, and the reaction was further continued for 2 hours at 75 ° C. The reaction solution was allowed to cool to room temperature, and 5 parts of methanol was added. The reaction mixture was transferred to a Soxhlet extractor and washed sequentially with 150 parts of methanol and 150 parts of hexane. Finally, the residue was extracted with 150 parts of chloroform, the solvent was distilled off, and poly {3- (2,5-dioxaheptyl) thiophene} (P-5) 2 having a stereoregularity of 96.7%. 0.85 part (yield 65.5%, total yield 30.4%) was obtained.

<Production Example 6>
Synthesis of poly {3- (2,5-dioxahexyl) thiophene} (P-6):
The stereoregularity was 97.4% in the same manner as in Production Example 5 except that 2.99 parts of 2-methoxyethanol [manufactured by Tokyo Chemical Industry Co., Ltd.] was used instead of 3.54 parts of 2-ethoxyethanol. There was obtained 2.40 parts of (P-6) (total yield 27.7%).

<Production Example 7>
Synthesis of poly {3- (2,5-dioxaoctyl) thiophene} (P-7):
The stereoregularity was 95.9% in the same manner as in Production Example 5 except that 4.09 parts of 2-propoxyethanol (manufactured by Tokyo Chemical Industry Co., Ltd.) was used instead of 3.54 parts of 2-ethoxyethanol. There was obtained 2.72 parts of (P-7) (total yield: 27.0%).

<Production Example 8>
Synthesis of poly {3- (2,5,8-trioxadecyl) thiophene} (P-8):
The stereoregularity was 95.8% in the same manner as in Production Example 5 except that 5.27 parts of diethylene glycol monoethyl ether (manufactured by Tokyo Chemical Industry Co., Ltd.) was used instead of 3.54 parts of 2-ethoxyethanol. There was obtained 3.13 parts of (P-8) (total yield 26.9%).

<Production Example 9>
Synthesis of poly {3- (2-oxapentyl) thiophene} (P-9):
The stereoregularity is 96.0% in the same manner as in Production Example 5 except that 2.36 parts of n-propanol (manufactured by Tokyo Chemical Industry Co., Ltd.) are used instead of 3.54 parts of 2-ethoxyethanol. 2.14 parts of (P-9) were obtained (total yield 27.2%).

<Production Example 10>
Synthesis of sulfonated poly (3-octyloxythiophene) lithium salt (P-10):
(1) Synthesis of sulfonated poly (3-octyloxythiophene);
180 parts of fuming sulfuric acid were mixed with 6.02 parts of (P-1) obtained in Production Example 1 and reacted at 85 ° C. for 24 hours. The reaction mixture was diluted with 6000 parts of distilled water and then stirred at room temperature for 1 hour to be dispersed. The dispersion was settled using a centrifuge, the supernatant was removed, and then washed twice with 800 parts of distilled water using a centrifuge. The obtained precipitate was put into 6000 parts of distilled water and dispersed by irradiating with ultrasonic waves for 30 minutes.
The obtained dispersion was passed through a column packed with 30 parts of an ion exchange resin (Anverjet 4400, manufactured by Aldrich). After removing residual sulfonic acid, water was distilled off under reduced pressure to obtain sulfonated poly (3- 7.12 g (96% yield) of octyloxythiophene was obtained.

(2) Synthesis of sulfonated poly (3-octyloxythiophene) lithium salt (P-10);
After 7.12 parts of the sulfonated poly (3-octyloxythiophene) was dispersed in 50 parts of distilled water, 0.55 part of lithium carbonate was added and reacted at room temperature for 1 hour. The reaction mixture was depressurized and water was distilled off to obtain 7.21 parts (99% yield, 95% overall yield) of sulfonated poly (3-octyloxythiophene) lithium salt (P-10).
As a result of analyzing the obtained sulfonated poly (3-octyloxythiophene) lithium salt by NMR, the content of the thiophene repeating unit (α1) was 49 mol%, and the content of the thiophene repeating unit (β1) was 51 mol%. there were.

<Production Example 11>
Synthesis of sulfonated poly {3- (2,5-dioxaheptyl) thiophene} lithium salt (P-11):
(P-1) A sulfonated poly {3- (2,2) in the same manner as in Production Example 10 except that 5.27 parts of (P-5) obtained in Production Example 5 were used instead of 6.02 parts. 5-87 parts of 5-dioxaheptyl) thiophene} lithium salt (P-11) was obtained (91% overall yield). The obtained sulfonated poly {3- (2,5-dioxaheptyl) thiophene} lithium salt was analyzed by NMR. As a result, the content of the thiophene repeating unit (α2) was 52 mol%, and the thiophene repeating unit (β2) The content was 48 mol%.

<Production Example 12>
Production of negative electrode;
92.5 parts of graphite powder having an average particle size of about 8 to 12 μm, 7.5 parts of polyvinylidene fluoride and 200 parts of 1-methyl-2-pyrrolidone [manufactured by Tokyo Chemical Industry Co., Ltd.] are thoroughly mixed in a mortar, and slurry Got. The obtained slurry was applied to one side of a 20 μm thick copper foil, dried at 100 ° C. for 15 minutes to evaporate the solvent, punched out to 12 mmφ, and made a negative electrode with a thickness of 30 μm using a press.

<Production Example 13>
Preparation of lithium ion secondary battery electrolyte;
LiPF6 was dissolved as an electrolyte in a mixed solvent of ethylene carbonate: diethyl carbonate: vinylene carbonate = 48.5: 48.5: 3 (weight ratio) to prepare an electrolyte solution.

Examples 1-15 and Comparative Examples 1-2
<Preparation of positive electrode>
Substituted polythiophenes obtained in the above Production Examples 1 to 11, polyvinylidene fluoride (PVDF), carboxymethyl cellulose (CMC) and polyaniline sulfonic acid (PAS) as a binding force-assisting polymer compound, and acetylene black as a conductive assistant ( Nippon Denka Co., Ltd., average particle size: 1.0 μm) (AB) prepared by mixing at a weight ratio shown in Table 1, 1.0 part of a binder, LiFePO ₄ powder 9.0 parts, 7.0 parts of methyl-2-pyrrolidone [manufactured by Tokyo Chemical Industry Co., Ltd.] was sufficiently kneaded in a mortar to obtain slurries for Examples 1 to 15 and Comparative Examples 1 and 2, respectively.
The obtained slurry was applied on one surface of an aluminum electrolytic foil having a thickness of 20 μm using a wire coating bar in the atmosphere, dried at 100 ° C. for 15 minutes, and further reduced in pressure (10 mmHg) at 80 ° C. for 5 minutes. It was dried for a minute to form a layer made of an active material and a binder having a thickness of 10 μm on the aluminum electrolytic foil, and a positive electrode having a total film thickness of 30 μm was produced.

<Preparation of secondary battery evaluation cell>
A secondary battery cell in which the positive electrode for Examples 1 to 15 and Comparative Examples 1 and 2 and the negative electrode obtained in Production Example 12 are arranged at both ends in a 2032 type coin cell so that the respective coated surfaces face each other. Was made. The electrolyte solution prepared in Production Example 13 was injected into the cell to obtain an evaluation cell.

[Evaluation example]
Using the obtained positive electrode and evaluation cell, the following evaluation methods were used to evaluate the binding force, battery output, capacity retention rate, capacity retention rate during high-speed charge / discharge, and cycle characteristic deterioration rate during high-speed charge / discharge. The results are shown in Table 1.

<Evaluation of binding power>
In accordance with the cross cut test method JIS K5400, a 10 × 10 square cross cut is made on the surface of the positive electrode film, and a cellophane adhesive tape (manufactured by Nichiban Co., Ltd.) is pasted and peeled off, and then bonded to the active material. The number of squares in which the layer made of the agent remained was counted visually, the binding force was calculated from the following formula, and the determination was made based on the following evaluation criteria.
Binding power (%) = (Number of remaining squares / 100) × 100
◎: Binding force (%) is 95% or more ○: Binding force (%) is 90 to less than 95% Δ; Binding force (%) is less than 50 to 90% ×: Binding force (%) is less than 50%

<Evaluation of battery output>
Using a charge / discharge measuring device “Battery Analyzer 1470” [manufactured by Toyo Technica Co., Ltd.], charge so that SOC (State of charge: ratio of capacity in fully charged state to capacity at a predetermined time) is 60%. Then, discharge at a constant current and read the voltage after 10 seconds. This operation is performed with several current values, and the current value is plotted on the horizontal axis and the voltage value after 10 seconds is plotted on the vertical axis to create an approximate line, and the current value (I3. The battery output was calculated from the following formula.
Battery output (W) = I3.0V × 3.0

<Evaluation of capacity retention>
And a charge-discharge measuring instrument was used "Battery Analyzer 1470 model", was charged from the voltage 0V by the current 0.2 mA / cm ² until 2V, after 10 minutes of resting, the battery voltage of the current 0.2 mA / cm ² 0V This charge / discharge was repeated 50 cycles.
At this time, the battery capacity at the first charge and the battery capacity at the 50th cycle charge are measured, and the capacity retention rate is calculated from the following equation. It shows that charging / discharging cycling characteristics are so favorable that a numerical value is large.
Capacity retention rate (%) = (battery capacity at the 50th cycle charge / battery capacity at the first charge) × 100

<Evaluation of capacity retention during high-speed charge / discharge>
And a charge-discharge measuring instrument was used "Battery Analyzer 1470 model", was charged from the voltage 0V by the current 0.5 mA / cm ² until 2V, after 10 minutes of resting, the battery voltage of the current 0.5 mA / cm ² 0V This charge and discharge was repeated.
At this time, the battery capacity at the time of initial charge and the battery capacity at the time of charge in the 50th cycle are measured, and the capacity retention rate at high speed charge / discharge is calculated from the following formula. It shows that a high-speed charge / discharge cycle characteristic is so favorable that a numerical value is large.
Fast charge / discharge capacity retention ratio (%) = (battery capacity at the 50th cycle charge / battery capacity at the first charge) × 100

<Evaluation of cycle characteristics deterioration rate during high-speed charge / discharge>
The cycle characteristic deterioration rate during high-speed charge / discharge was calculated based on the following formula. The larger the value, the better the cycle characteristics at the time of high speed charge / discharge compared with the normal charge / discharge.
Cycle characteristic deterioration rate during high-speed charge / discharge (%) = (high-speed charge / discharge capacity retention ratio / capacity retention ratio) × 100
The capacity retention rate is a volume retention rate measured and calculated in the above <Evaluation of capacity retention rate>.

  From Table 1, the binder for positive electrodes of the present invention has a coating force applied to the aluminum electrolytic foil surface that can sufficiently withstand the use, and the positive electrodes produced using these positive electrode binders are It can be seen that the output characteristics are excellent and the cycle characteristics are good even during high-speed charge / discharge.

  Since the binder for a lithium ion secondary battery positive electrode of the present invention is excellent in electron conductivity and ion conductivity, it is also useful as a binder for batteries other than lithium ion secondary batteries. Moreover, since the lithium ion secondary battery using the binder of the present invention is excellent in output and safety, it is useful for electric vehicles.

Claims (6)

A binder for a positive electrode of a lithium ion secondary battery (A), comprising a substituted polythiophene (P) and a polymer compound that assists the binding force,
The substituted polythiophene (P) is
At least some of the thiophene repeat units are
(A) a polyether group having 1 to 9 repeating units composed of an oxyalkylene group having 2 to 4 carbon atoms, one end of which is an alkoxy group having 1 to 15 carbon atoms,
(B) an alkoxy group,
(C) an alkoxyalkyl group or (d) a thiophene repeating unit (α) substituted at the 3-position and / or 4-position of the thiophene ring by an alkyl group substituted with the polyether group (a) ; A substituted polythiophene (P21) having a thiophene repeating unit (α1) represented by the following general formula (1) and a thiophene repeating unit (β1) represented by the following general formula (3); A substituted polythiophene (P22) having a thiophene repeating unit (α2) represented by formula (4) and a thiophene repeating unit (β2) represented by the following general formula (4);
The polymer compound that assists the binding force is polyvinylidene fluoride or carboxymethyl cellulose,
The binder (A):

[ Wherein , OR ¹ and OR ⁴ each independently represents an oxyethylene group, an oxypropylene group or an oxybutylene group, and R ² and R ⁵ each independently represents a linear or branched alkyl group having 1 to 12 carbon atoms. R ³ represents a linear or branched alkylene group having 1 to 4 carbon atoms, and n and m are each independently an integer of 0 to 5. ];

[ Wherein , OR ¹ and OR ⁴ each independently represent an oxyethylene group or an oxypropylene group, R ² and R ⁵ each independently represent a linear or branched alkyl group having 1 to 12 carbon atoms, R ³ Represents a linear or branched alkylene group having 1 to 4 carbon atoms, M ⁺ represents an alkali metal cation or a proton, and n and m are each independently an integer of 0 to 5. ] In the thiophene repeating unit (α1), OR ¹ in the general formula (1) is an oxyethylene group, and when n is 0, R ² is a linear or branched alkyl group having 3 to 12 carbon atoms, When n is 1 or more, R ² is a linear or branched alkyl group having 1 to 6 carbon atoms, and the thiophene repeating unit (α2) is represented by R ³ in the general formula (2). 1 to 3 alkylene groups, OR ⁴ is an oxyethylene group, and when m is 0, R ⁵ is a linear or branched alkyl group having 3 to 12 carbon atoms, and m is 1 or more. binder according to claim 1, wherein R ⁵ is one that is linear or branched alkyl group having 1 to 6 carbon atoms in the case. The binder according to claim 1 or 2, wherein the content of the thiophene repeating unit (α) in the substituted polythiophene (P) is 50 to 100 mol% in the substituted polythiophene (P). The binder according to any one of claims 1 to 3 , wherein the stereoregularity defined by a percentage of head-to-tail-head-to-tail bonds in the substituted polythiophene (P) is 90% or more. A positive electrode material for a lithium ion secondary battery obtained by binding the active material (B) to the current collector (C) with the binder according to any one of claims 1 to 4 . The positive electrode material according to claim 5 , wherein the active material (B) is a lithium transition metal composite oxide.