WO2010079565A1 - 非水電解液二次電池 - Google Patents
非水電解液二次電池 Download PDFInfo
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- WO2010079565A1 WO2010079565A1 PCT/JP2009/007157 JP2009007157W WO2010079565A1 WO 2010079565 A1 WO2010079565 A1 WO 2010079565A1 JP 2009007157 W JP2009007157 W JP 2009007157W WO 2010079565 A1 WO2010079565 A1 WO 2010079565A1
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0566—Liquid materials
- H01M10/0567—Liquid materials characterised by the additives
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0566—Liquid materials
- H01M10/0568—Liquid materials characterised by the solutes
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- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Definitions
- the present invention generally relates to a non-aqueous electrolyte secondary battery provided with a non-aqueous electrolyte containing a non-aqueous solvent and an electrolyte, and more specifically, non-aqueous electrolysis with an improved composition of additives to the non-aqueous electrolyte.
- the present invention relates to a liquid secondary battery.
- a non-aqueous electrolyte secondary battery for example, a non-aqueous electrolyte obtained by dissolving a lithium salt such as lithium hexafluorophosphate as an electrolyte in a non-aqueous solvent such as dimethyl carbonate is used.
- a non-aqueous electrolyte solution obtained by dissolving a lithium salt such as lithium hexafluorophosphate as an electrolyte in a non-aqueous solvent such as dimethyl carbonate is used.
- various additives are added to such a non-aqueous electrolyte solution.
- Patent Document 1 Japanese Patent Application Laid-Open No. 2007-165125 discloses a technique for improving durability such as cycle characteristics and high-temperature storage and suppressing an increase in internal resistance so that it can be used for power applications.
- Electrolytic solutions for nonaqueous electrolyte batteries and nonaqueous electrolyte batteries have been proposed.
- This non-aqueous electrolyte battery electrolyte is a non-aqueous electrolyte battery electrolyte composed of a non-aqueous organic solvent and a solute.
- bis (oxalato) borate difluoro (oxalato) borate
- at least one compound selected from the second compound group At least one compound selected from the second compound group.
- Patent Document 1 a charge / discharge cycle test is performed at a high temperature by using one lithium salt having an oxalato complex as an anion and one fluorophosphate as an additive in an electrolyte for a non-aqueous electrolyte battery. It is described that the capacity retention rate after repeating the above can be improved, and the increase in internal resistance and the generation of gas can be suppressed.
- Patent Document 1 Even if the additive described in Patent Document 1 is used, there is a limit to improving the capacity retention rate after repeating the charge / discharge cycle at a high temperature in the nonaqueous electrolyte battery.
- Patent Document 1 does not specifically disclose an example of a non-aqueous electrolyte secondary battery using two types of lithium salts having an oxalato complex as an anion. In such an example, The capacity maintenance rate after repeating the charge / discharge cycle at a high temperature is not evaluated at all.
- an object of the present invention is to improve the capacity retention rate after repeating the charge / discharge cycle at a high temperature in a non-aqueous electrolyte secondary battery including a non-aqueous electrolyte containing a non-aqueous solvent and an electrolyte. It is providing the composition of the additive with respect to non-aqueous electrolyte solution.
- a non-aqueous electrolyte secondary battery is a non-aqueous electrolyte secondary battery including a non-aqueous electrolyte containing a non-aqueous solvent and an electrolyte, and is an oxalato complex with respect to the non-aqueous electrolyte. At least two types of lithium salt having an anion as an anion are added.
- the non-aqueous electrolyte secondary battery of the present invention at least two types of lithium salts having an oxalato complex as an anion are added to the non-aqueous electrolyte so that the charge / discharge cycle is repeated at a high temperature.
- the capacity retention ratio that is, the high temperature cycle characteristics can be improved.
- At least two types of lithium salts are Li [M (C 2 O 4 ) x R y ] (wherein M consists of P, B, Al, Si, and C).
- R is one group selected from the group consisting of a halogen group, an alkyl group and a halogenated alkyl group, x is a positive integer, and y is 0 or a positive integer) It is preferable.
- the two lithium salts are lithium bisoxalate borate (Li [B (C 2 O 4 ) 2 ]).
- the lithium bisoxalate borate is 0.3 parts by weight or more and 3.0 parts by weight or less and difluoro (bisoxalato) with respect to 100 parts by weight of the nonaqueous electrolyte. It is preferable that 0.3 to 2.0 parts by weight of lithium phosphate is added.
- the lithium bisoxalate borate is 0.5 parts by weight or more and 1.5 parts by weight or less and difluoro (bisoxalato) with respect to 100 parts by weight of the nonaqueous electrolyte. It is preferable that 0.5 to 1.0 part by weight of lithium phosphate is added.
- the high-temperature cycle characteristics can be further improved.
- a non-aqueous electrolyte secondary battery including a non-aqueous electrolyte containing a non-aqueous solvent and an electrolyte
- the capacity retention rate after repeated charge / discharge cycles at a high temperature is improved. Therefore, it is possible to provide a composition of additives for the non-aqueous electrolyte solution.
- the inventor of the present application conducted various studies on the composition of the additive to the non-aqueous electrolyte solution for improving the capacity retention rate after repeating the charge / discharge cycle at a high temperature. As a result, it has been found that if at least two types of lithium salts having an oxalato complex as an anion are used and added to a non-aqueous electrolyte, the capacity retention rate after repeated charge / discharge cycles at high temperatures can be improved.
- the present invention has been made based on such knowledge of the present inventor.
- lithium bisoxalate borate Li [B (C 2 O 4 ) 2 ]
- the lithium bisoxalate borate is 0.3 parts by weight or more and 3.0 parts by weight or less and difluoro (bisoxalato) phosphorus with respect to 100 parts by weight of the nonaqueous electrolytic solution.
- Lithium acid is added in an amount of 0.3 to 2.0 parts by weight.
- the lithium bisoxalate borate is 0.5 parts by weight or more and 1.5 parts by weight or less and the difluoro (bisoxalate) lithium phosphate is 0.5 parts by weight with respect to 100 parts by weight of the nonaqueous electrolytic solution.
- the capacity retention rate after repeating the charge / discharge cycle at a high temperature can be further improved.
- a non-aqueous electrolyte secondary battery includes a non-aqueous electrolyte obtained by dissolving an electrolyte in a non-aqueous solvent, a positive electrode, and a negative electrode.
- non-aqueous solvent dimethyl carbonate, ethyl methyl carbonate, ethylene carbonate, propylene carbonate, butylene carbonate, diethyl carbonate and the like can be used alone or in combination of two or more.
- chain ester systems such as methyl formate, ethyl formate, methyl acetate, and ethyl acetate, cyclic ester systems such as ⁇ -butyrolactone, and cyclic sulfones such as sulfolane may be included.
- LiPF 6, LiAsF 6, LiBF 4 , LiCF 3 SO 3, LiC (SO 2 CF 3) 3, LiN (SO 2 C 2 F 5) 2, LiN (SO 2 CF 3) 2 , etc. can be used alone, or two or more can be used in combination.
- the positive electrode and the negative electrode are alternately stacked via separators.
- the structure of the battery element may be composed of a stack of a plurality of strip-shaped positive electrodes, a plurality of strip-shaped separators and a plurality of strip-shaped negative electrodes, a stack of so-called single-wafer structures. It may be configured by folding and interposing a strip-shaped positive electrode and a strip-shaped negative electrode alternately.
- a winding type structure in which a long positive electrode, a long separator, and a long negative electrode are wound may be employed. In the following examples, a wound structure is adopted as the structure of the battery element.
- the positive electrode is formed by laminating a positive electrode active material on both surfaces of a positive electrode current collector.
- the positive electrode current collector is made of aluminum.
- the positive electrode active materials are lithium cobalt oxide composite oxide (LCO), lithium manganate composite oxide (LMO), lithium nickelate composite oxide (LNO), lithium-nickel-manganese-cobalt composite oxide (LNMCO), lithium A manganese-nickel composite oxide (LMNO), a lithium-manganese-cobalt composite oxide (LMCO), a lithium-nickel-cobalt composite oxide (LNCO), or the like can be used.
- the positive electrode active material may be a mixture of the above materials.
- the positive electrode active material may be an olivine-based material such as LiFePO 4 .
- the negative electrode is formed by laminating a negative electrode active material on both surfaces of a negative electrode current collector.
- the negative electrode current collector is made of copper
- the negative electrode active material is made of a carbon material.
- the carbon material of the negative electrode active material graphite, hard carbon, soft carbon, or the like is used.
- the negative electrode active material may be a mixture of the above materials.
- the negative electrode active material may be a ceramic such as lithium titanate or an alloy-based material such as Si or Sn.
- the separator is not particularly limited, and a conventionally known separator can be used.
- the separator is not limited by its name, and a solid electrolyte or gel electrolyte having a function (role) as a separator may be used instead of the separator.
- a separator containing an inorganic material such as alumina or zirconia may be used.
- the composition of the additive with respect to the non-aqueous electrolyte is changed as shown in Table 1 below, and compared with Examples 1 to 11.
- Nonaqueous electrolyte secondary batteries of Examples 1 to 7 were produced.
- Lithium-nickel-manganese-cobalt composite oxide represented by the composition formula LiNi 1/3 Mn 1/3 Co 1/3 O 2 as a positive electrode active material, carbon as a conductive additive, and as a binder
- a slurry was prepared by blending polyvinylidene fluoride (PVDF) in a weight ratio of 90: 7: 3 and kneading with N-methyl 2-pyrrolidone (NMP). This slurry was applied to both surfaces of an aluminum foil as a current collector, dried, and then rolled with a roll press to produce a positive electrode.
- PVDF polyvinylidene fluoride
- NMP N-methyl 2-pyrrolidone
- a natural graphite powder as a negative electrode active material and PVDF as a binder were blended in a weight ratio of 95: 5 and kneaded with NMP to prepare a slurry. This slurry was applied to both sides of a copper foil as a current collector, dried, and then rolled with a roll press to produce a negative electrode.
- the solvent was prepared by preparing dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), and ethylene carbonate (EC) at a volume ratio of 1: 1: 1.
- a nonaqueous electrolytic solution was prepared by dissolving lithium hexafluorophosphate (LiPF 6 ) as an electrolyte at a rate of 1 mol / L in this solvent.
- Lithium bisoxalate borate (Li [B (C 2 O 4 ) 2 ]) and difluoro (bisoxalato) lithium phosphate (Li [PF] are added to 100 parts by weight of the nonaqueous electrolyte solution in the obtained nonaqueous electrolyte solution.
- 2 (C 2 O 4 ) 2 ]) is added in parts by weight shown in Table 1 to prepare a non-aqueous electrolyte containing the additive.
- Lead tabs were provided on the positive electrode and the negative electrode produced above. What was wound in a flat shape with a porous separator interposed between the positive electrode and the negative electrode was accommodated in an outer packaging material made of a laminate film containing aluminum as an intermediate layer. Thereafter, the non-aqueous electrolyte prepared above was injected into the outer packaging material, and then the opening of the outer packaging material was sealed to produce a non-aqueous electrolyte secondary battery having a battery capacity of 260 mAh.
- the capacity retention rate after 100 charge / discharge cycles at a temperature of 60 ° C. was measured. Specifically, after charging each battery until the voltage reaches 4.2V under an atmosphere at a temperature of 60 ° C. with a charging current of 500 mA, the charging current is further reduced while the voltage is maintained at 4.2V. Each battery was charged until the current reached 12.5 mA. Then, the discharge capacity was measured when each battery was discharged until the voltage became 2.5 V with a discharge current of 500 mA. Such charge / discharge was repeated 100 cycles. The ratio of the discharge capacity measured after 100 cycles to the discharge capacity measured after 1 cycle was calculated by the following formula, and the obtained value was evaluated as the capacity retention rate (%) after 100 cycles.
- Capacity retention rate (%) ⁇ (discharge capacity after 100 cycles) / (discharge capacity after 1 cycle) ⁇ ⁇ 100
- the lithium bisoxalate borate is 0.5 parts by weight or more and 1.5 parts by weight or less and 100% by weight of the non-aqueous electrolyte solution and difluoro It can be seen that high temperature cycle characteristics can be further improved by adding 0.5 parts by weight or more and 1.0 parts by weight or less of (bisoxalato) lithium phosphate.
- a non-aqueous electrolyte secondary battery comprising a non-aqueous electrolyte containing a non-aqueous solvent and an electrolyte
- a non-aqueous system for improving the capacity retention rate after repeated charge / discharge cycles at a high temperature Since the composition of the additive with respect to the electrolytic solution can be provided, the present invention can be applied to a non-aqueous electrolyte secondary battery in which the additive is included in the non-aqueous electrolytic solution.
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Abstract
Description
正極活物質として組成式LiNi1/3Mn1/3Co1/3O2で表されるリチウム-ニッケル-マンガン-コバルト複合酸化物(LNMCO)と、導電助剤としての炭素と、バインダーとしてのポリフッ化ビニリデン(PVDF)とを重量比率で90:7:3になるように配合して、N-メチル2-ピロリドン(NMP)と混錬することにより、スラリーを作製した。このスラリーを、集電体としてのアルミニウム箔の両面に塗布し、乾燥させた後、ロールプレスにて圧延することによって正極を作製した。
負極活物質としての天然黒鉛粉末と、バインダーとしてのPVDFとを重量比率で95:5になるように配合して、NMPと混錬することにより、スラリーを作製した。このスラリーを、集電体としての銅箔の両面に塗布し、乾燥させた後、ロールプレスにて圧延することによって負極を作製した。
溶媒は、ジメチルカーボネート(DMC)とエチルメチルカーボネート(EMC)とエチレンカーボネート(EC)とを体積比率で1:1:1になるように調製することにより準備した。この溶媒に、電解質としての六フッ化リン酸リチウム(LiPF6)を1mol/Lの割合で溶解させることにより、非水系電解液を作製した。
上記で作製した正極と負極にリードタブを設けた。この正極と負極の間に多孔性セパレータを介在させて扁平状に捲回したものを、アルミニウムを中間層として含むラミネートフィルムからなる外包材の内部に収納した。その後、上記で作製した非水系電解液を外包材の内部に注入した後、外包材の開口部を封止することにより、電池容量が260mAhの非水電解液二次電池を作製した。
充電電流を75mAとして電圧が4.2Vになるまで各電池に充電した後、さらに電圧を4.2Vに維持した状態で充電電流を減少させ、充電電流が12.5mAになるまで各電池に充電した。そして、放電電流を250mAとして電圧が2.5Vになるまで各電池を放電したときの初回放電容量を測定した。
高温サイクル特性として、温度60℃で充放電サイクルを100サイクル繰り返した後の容量維持率を測定した。具体的には、温度60℃の雰囲気下において充電電流を500mAとして電圧が4.2Vになるまで各電池に充電した後、さらに電圧を4.2Vに維持した状態で充電電流を減少させ、充電電流が12.5mAになるまで各電池に充電した。そして、放電電流を500mAとして電圧が2.5Vになるまで各電池を放電したときの放電容量を測定した。このような充放電を1サイクルとして100サイクル繰り返した。1サイクル後に測定した放電容量に対する、100サイクル後に測定した放電容量の割合を次の式で算出し、得られた値を100サイクル後の容量維持率(%)として評価した。
Claims (5)
- 非水系溶媒と電解質とを含む非水系電解液を備えた非水電解液二次電池であって、
前記非水系電解液に対して、オキサラト錯体をアニオンとするリチウム塩が少なくとも2種類添加されている、非水電解液二次電池。 - 前記リチウム塩は、Li[M(C2O4)xRy](式中、MはP、B、Al、SiおよびCからなる群より選択される1種、Rはハロゲン基、アルキル基およびハロゲン化アルキル基からなる群より選択される1種の基、xは正の整数、yは0または正の整数である)である、請求項1に記載の非水電解液二次電池。
- 前記リチウム塩は、リチウムビスオキサレートボレート(Li[B(C2O4)2])とジフルオロ(ビスオキサラト)リン酸リチウム(Li[PF2(C2O4)2])である、請求項2に記載の非水電解液二次電池。
- 前記非水系電解液100重量部に対して、リチウムビスオキサレートボレートが0.3重量部以上3.0重量部以下、かつ、ジフルオロ(ビスオキサラト)リン酸リチウムが0.3重量部以上2.0重量部以下添加されている、請求項3に記載の非水電解液二次電池。
- 前記非水系電解液100重量部に対して、リチウムビスオキサレートボレートが0.5重量部以上1.5重量部以下、かつ、ジフルオロ(ビスオキサラト)リン酸リチウムが0.5重量部以上1.0重量部以下添加されている、請求項4に記載の非水電解液二次電池。
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JP2010545638A JP5278442B2 (ja) | 2009-01-06 | 2009-12-24 | 非水電解液二次電池 |
CN2009801539064A CN102273000A (zh) | 2009-01-06 | 2009-12-24 | 非水电解液二次电池 |
US13/170,652 US20110256458A1 (en) | 2009-01-06 | 2011-06-28 | Non-Aqueous Electrolyte Secondary Battery |
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US13/170,652 Continuation US20110256458A1 (en) | 2009-01-06 | 2011-06-28 | Non-Aqueous Electrolyte Secondary Battery |
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JP2012064397A (ja) * | 2010-09-15 | 2012-03-29 | Toyota Central R&D Labs Inc | リチウムイオン二次電池 |
JP2012094369A (ja) * | 2010-10-27 | 2012-05-17 | Shin Etsu Chem Co Ltd | 非水電解液二次電池 |
JPWO2012086507A1 (ja) * | 2010-12-24 | 2014-05-22 | 株式会社村田製作所 | 非水電解液二次電池 |
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JP2012182131A (ja) * | 2011-02-10 | 2012-09-20 | Mitsubishi Chemicals Corp | 二次電池用非水系電解液及びそれを用いた非水系電解液二次電池 |
US11205802B2 (en) | 2011-02-10 | 2021-12-21 | Mitsubishi Chemical Corporation | Non-aqueous electrolyte solution and non-aqueous electrolyte secondary battery employing the same |
US10476106B2 (en) | 2011-02-10 | 2019-11-12 | Mitsubishi Chemical Corporation | Non-aqueous electrolyte solution and non-aqueous electrolyte secondary battery employing the same |
US9923238B2 (en) | 2011-02-10 | 2018-03-20 | Mitsubishi Chemical Corporation | Non-aqueous electrolyte solution and non-aqueous electrolyte secondary battery employing the same |
JP2017010938A (ja) * | 2011-05-11 | 2017-01-12 | 株式会社Gsユアサ | 蓄電素子 |
US20140176074A1 (en) * | 2011-05-11 | 2014-06-26 | Gs Yuasa International Ltd. | Electric Storage Device |
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JP2012253010A (ja) * | 2011-05-11 | 2012-12-20 | Gs Yuasa Corp | 蓄電素子 |
JP2013089445A (ja) * | 2011-10-18 | 2013-05-13 | Toyota Motor Corp | 非水電解液二次電池及びその製造方法 |
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JP2014035892A (ja) * | 2012-08-09 | 2014-02-24 | Sanyo Electric Co Ltd | 非水電解質二次電池 |
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JP2014056667A (ja) * | 2012-09-11 | 2014-03-27 | Toyota Motor Corp | 非水電解質二次電池およびその製造方法 |
JP2016146341A (ja) * | 2015-02-02 | 2016-08-12 | 三菱化学株式会社 | 非水系電解液及び非水系電解液二次電池 |
JP2017004947A (ja) * | 2015-06-09 | 2017-01-05 | ステラケミファ株式会社 | 二次電池用非水電解液及びそれを備えた二次電池 |
WO2021205750A1 (ja) * | 2020-04-07 | 2021-10-14 | 太陽誘電株式会社 | 電気化学デバイス用電解液および電気化学デバイス |
JP7550562B2 (ja) | 2020-07-30 | 2024-09-13 | 三井化学株式会社 | リチウム二次電池用非水電解液、リチウム二次電池前駆体、リチウム二次電池、及びリチウム二次電池の製造方法 |
Also Published As
Publication number | Publication date |
---|---|
US20110256458A1 (en) | 2011-10-20 |
JP5278442B2 (ja) | 2013-09-04 |
CN102273000A (zh) | 2011-12-07 |
JPWO2010079565A1 (ja) | 2012-06-21 |
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