• 专利附录
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    • 专利摘要:
    The invention relates to an electrolyte composition, comprising: - a lithium bis (fluorosulfonyl) imide salt and / or a salt of lithium 2-trifluoromethyl-4,5-dicyanoimidazolate; and - a solvent of formula (I): in which: n is an integer ranging from 0 to 15, - R1, R2 and R3 independently represent a halogen atom or a linear or branched C1-C6 alkyl group, X represents either a covalent bond or a linear or branched C1 to C6 alkylene, alkenylene or alkynylene group; Y represents either a - (OCH2CH2) m - group or a - (N (CH3) CH2CH2) m - group, wherein m is an integer from 0 to 15 with the proviso that m is other than 0 when X is a covalent bond, and R4 is cyano, cyanate, isocyanate, thiocyanate or isothiocyanate.
    公开号:FR3033945A1
    申请号:FR1552122
    申请日:2015-03-16
    公开日:2016-09-23
    发明作者:Gregory Schmidt
    申请人:Arkema France SA；
    IPC主号:
    专利说明:

    [0001] FIELD OF THE INVENTION The present invention relates to an electrolyte formulation based on a particular lithium salt, namely lithium bis (fluorosulfonyl) imide (LiFSI) and / or Lithium 2-trifluoromethyl-4,5-dicarbonitrile-imidazolate (LiTDI) in combination with a silane solvent, as well as the use of this formulation in a Li-ion battery.
    [0002] TECHNICAL BACKGROUND An elementary cell of a Li-ion secondary battery (or lithium battery) comprises an anode (at the discharge), generally made of lithium metal or carbon-based, and a cathode (at the discharge), generally into a metal oxide type lithium insertion compound such as LiMn 2 O 4, LiCoO 2 or LiNiO 2. Between the anode and the cathode is interposed a conductive electrolyte lithium ions. In the case of the cathode, the metal oxide is generally deposited on an aluminum current collector. In use, that is to say during the discharge of the battery, the lithium released by oxidation at the (-) pole by the ionic anode Li, migrates through the conductive electrolyte and is inserted by a reduction reaction in the crystal lattice of the active material of the cathode at the (+) pole. The passage of each Li + ion in the internal circuit of the accumulator is exactly compensated by the passage of an electron in the external circuit, generating an electric current that can be used to power various devices in the field of portable electronics such as computers or telephones, or in the field of applications with higher power and energy density, such as electric vehicles. The electrolyte generally consists of a lithium salt dissolved in a solvent, which is generally a mixture of organic carbonates, offering a good compromise between the viscosity and the dielectric constant. Additives may be added to improve the stability of the electrolyte salts.
    [0003] The most currently used salt is LiPF6 salt; but it has many disadvantages such as limited thermal stability, instability to hydrolysis, and therefore lower battery safety. On the other hand, it has the advantage of forming a passivation layer on aluminum and of having a high ionic conductivity. Other salts, having the FSO 2 - group, have been proposed. They have demonstrated many advantages, including better ionic conductivity and resistance to hydrolysis. One of these salts, LiFSI (LiN (FSO2) 2) has shown very interesting properties that make it a good candidate for replacing LiPF6. LiFSI also forms a passivation layer, but more slowly and very sensitively to the purity of the product (see H-B Han, J. Power Sources 196, 3623-3632 (2011)). Another salt has also been proposed, namely lithium LiTDI (or 2-trifluoromethyl-4,5-dicarbonitrile-imidazolate). This salt has the advantage of having fewer fluorine atoms and having strong carbon-fluorine bonds, which makes it possible to avoid or reduce the formation of HF during the thermal or electrochemical degradation of the salt. . WO 2010/023413 shows that this salt has a conductivity of the order of 6 mS / cm, a very good dissociation between the imidazolate anion and the lithium cation, hence its use as an electrolyte salt. Li-ion batteries. On the other hand, the salt has a strong irreversible capacity without addition of additive for the formation of the solid-electrolyte interphase (SEI) on the graphite. Moreover, document US 2014/0356735 has shown the interest of silane solvents in certain electrolytes. The document illustrates in particular that the addition of the solvent in an electrolyte based on certain salts such as LiPF6 makes it possible to improve certain performances of the Li-ion battery. There is a need to provide electrolytes to further improve the performance of the Li-ion battery. In particular, there is a need to provide electrolytes to passivate (i.e., protect against corrosion) the cathode. There is also a need to provide electrolytes to reduce the irreversible capacity of the Li-ion battery. SUMMARY OF THE INVENTION The invention primarily relates to an electrolyte composition, comprising: a lithium bis (fluorosulfonyl) imide salt and / or a 2-trifluoromethyl-4,5-dicyano salt; lithium imidazolate; and a solvent of formula (I) in which: n is an integer ranging from 0 to 15, - R1, R2 and R3 independently represent a halogen atom or a hydrogen atom; C1-C6 linear or branched alkyl group; X represents either a covalent bond or a linear or branched C 1 -C 6 alkylene, alkenylene or alkynylene group; Y represents either a - (OCH 2 CH 2) - group or a group - (N (CH3) CH2CH2) m-, m being an integer from 0 to 15, with the proviso that m is different from 0 when X is a covalent bond, and 15 - R4 represents a cyano, cyanate, isocyanate, thiocyanate group or isothiocyanate. According to one embodiment, the solvent of formula (I) is more precisely of formula (II): ## STR2 ## in which: n and m are integers ranging from 1 to 15; R1, R2 and R3 independently represent a halogen atom or a C1-C6 linear or branched alkyl group, and R4 represents a cyano, cyanate, isocyanate, thiocyanate or isothiocyanate group. The solvent of formula (I) is more particularly of formula (III): ## STR2 ## in which: X represents either a covalent bond or an alkylene, alkenylene or alkenylene group; C1-C6 linear or branched alkynylene; R1, R2 and R3 independently represent a halogen atom or a linear or branched C1-C6 alkyl group; and -R4 represents a cyano, cyanate, isocyanate, thiocyanate or isothiocyanate group According to one embodiment, the solvent of formula (I) is Specifically of formula (IV): wherein X represents either a covalent bond or a linear or branched C1 to C6 alkylene, alkenylene or alkynylene group; m represents an integer equal to from 1 to 15, - R1, R2 and R3 independently represent a halogen atom or a linear or branched C1-C6 alkyl group, and - R4 represents a cyano, cyanate, isocyanate, thiocyanate or isothiocyanate group. According to one embodiment, the solvent of formula (I) is more precisely of formula (V): (V) OCH 2 CH 2) mR 4 in which: X represents either a covalent bond or a linear or branched alkylene, alkenylene or alkynylene group; at C1 to C6, m represents an integer from 1 to 15, R1, R2 and R3 independently represent a halogen atom or a linear or branched C1 to C6 alkyl group, and R4 represents a cyano, cyanate, isocyanate, thiocyanate or isothiocyanate group. According to one embodiment, the solvent of formula (I) is more precisely of formula (IIIa): ## STR2 ## According to one embodiment, the mass concentration of bis (fluorosulfonyl) imide salt Lithium and / or lithium 2-trifluoromethyl-4,5-dicyanoimidazolate salt in the composition is 0.5 to 16%.
    [0004] According to one embodiment, the mass concentration of solvent of formula (I) in the composition is 0.5 to 5%. According to one embodiment, the composition also comprises at least one additional solvent, and preferably a mixture of two or three additional solvents, chosen from carbonates, glymes, nitriles, dinitriles, fluorinated solvents, and combinations of these ; and the composition more preferably comprises a mixture of carbonates, such as a mixture of ethylene carbonate and diethyl carbonate. According to one embodiment, the composition comprises another lithium salt, preferably chosen from the salts LiPF6, LiBF4, CH3COOL1, CH3SO3Li, CF3SO3Li, CF3COOL1, Li21312F12 and LiBC408. According to one embodiment, the mass concentration of other lithium salt is less than or equal to 15.5%. The invention also relates to a battery comprising at least one cell which comprises a cathode, an anode and the electrolyte composition 25 described above, interposed between the cathode and the anode. The present invention overcomes the disadvantages of the state of the art. It more particularly provides electrolytes imparting improved performance to a Li-ion battery, particularly in terms of passivation of the cathode and in terms of reducing the irreversible capacity of the battery. This is accomplished through the use of a silane solvent in combination with LiFSI or LiTDI lithium salt. In particular, it has been found that the use of a silane solvent in combination with LiFSI makes it possible to eliminate corrosion problems due to impurities present in LiFSI; and, in the case of high purity LiFSI, to accelerate the formation of the passivation layer on the metal of the cathode. This passivation layer is essential for the proper functioning of the Li-ion battery. Indeed, without this layer, the capacity of the Li-ion battery would decrease rapidly during the time of use.
    [0005] It has also been discovered that, in the case of LiTDI, the addition of silane solvent reduces the irreversible capacity of the Li-ion battery. The SEI, mentioned above, is a polymeric layer formed at the electrolyte / electrode interface during the first cycle. This SEI is essential for the operation of the battery and the quality of this SEI directly influences the life of the battery. With the use of a silane solvent, an irreversible gain in capacity of several percent can be obtained. BRIEF DESCRIPTION OF THE FIGURES FIG. 1 represents, with reference to Example 1, the oxidation current (in ordinates, in pA) as a function of the potential with respect to the Li / Li + pair (in the abscissa, in FIG. V) in a Li-ion battery according to the invention (curves I) and in a comparative Li-ion battery (curves C). DESCRIPTION OF EMBODIMENTS OF THE INVENTION The invention is now described in more detail and in a nonlimiting manner in the description which follows. All proportions indicated in the application are mass proportions unless otherwise indicated. The electrolyte of the invention comprises one or more lithium salts and one or more solvents. Among the lithium salts is at least lithium bis (fluorosulfonyl) imide (LiFSI) or lithium 2-trifluoromethyl-4,5-dicyanoimidazolate (LiTDI). It is also possible to use a mixture of LiFSI and LiTDI. The total content of LiFSI and LiTDI is preferably from 0.5 to 16% by weight relative to the total electrolyte composition, more preferably from 1 to 12%, and especially from 2 to 8%. Other additional lithium salts may also be present. They may in particular be chosen from the salts LiPF6, LiBF4, CH3COOL1, CH3SO3Li, CF3SO3Li, CF3COOL1, Li2B12F12 and LiBC408.
    [0006] The total content of additional lithium salts is preferably less than or equal to 16% by weight relative to the total composition, preferably less than or equal to 10%, or 5%, or 2%, or 1%. .
    [0007] Preferably, LiFSI and / or LiTDI are predominant, by weight, among the total lithium salts of the electrolyte composition. According to one embodiment, the only lithium salt present in the electrolyte is LiFSI.
    [0008] According to one embodiment, the only lithium salt present in the electrolyte is LiTDI. According to one embodiment, the only lithium salts present in the electrolyte are LiFSI and LiTDI. The molar concentration of lithium salts in the electrolyte may range, for example, from 0.01 to 5 mol / L, preferably from 0.1 to 2 mol / L, more particularly from 0.5 to 1.5 mol / L. The molar concentration of LiFSi and / or LiTDI in the electrolyte may range, for example, from 0.01 to 5 mol / l, preferably from 0.1 to 2 mol / l, more particularly from 0.3 to 1.5 mol. / L.
    [0009] The electrolyte comprises one or more solvents. It comprises at least one silane solvent, and preferably also one or more solvents which may be in particular organic carbonates, glymes, nitriles and / or fluorinated solvents. The organic carbonates may be especially selected from ethylene carbonate, dimethyl carbonate, ethyl methyl carbonate, diethyl carbonate, propylene carbonate and combinations thereof. The glymes may in particular be chosen from ethylene glycol dimethyl ether, diethylene glycol t-butyl methyl ether and combinations thereof. Nitriles (including dinitrile compounds) may be selected from acetonitrile, methoxypropionitrile, propionitrile, butyronitrile, isobutyronitrile, valeronitrile, malononitrile, succinonitrile, glutaronitrile and combinations thereof. The fluorinated solvents may be carbonates, glymes or nitriles compounds described above, to which at least one hydrogen atom has been substituted by at least one fluorine atom.
    [0010] A mixture of ethylene carbonate and diethyl carbonate in a volumetric dimethyl ether ratio may advantageously be used in the electrolyte composition, the diethylene glycol dibutyl ether, the tetraethylene glycol being preferably from 0.1 to 2, more preferably from 0.2 to 1, and in particular from 0.3 to 0.5. The silane solvent has the general formula (I): ## STR1 ## In this formula: n is an integer ranging from 0 to 15, R1, R2 and R3 independently represent an atom of halogen or a linear or branched C1-C6 alkyl group; - X represents either a covalent bond or a linear or branched C1 to C6 alkylene, alkenylene or alkynylene group, - Y represents either a group - (OCH2CH2), - or - (N (CH 3) CH 2 CH 2) m -, wherein m is an integer from 0 to 15 with the proviso that m is other than 0 when X is a covalent bond, and - R 4 is a cyano group cyanate, isocyanate, thiocyanate or isothiocyanate. Preferably, n is 0 to 10, or 0 to 5, or 0 to 2, or 0 to 1. More preferably, n is 0 (i.e., R2 is connected to the Si atom by a simple covalent bond).
    [0011] Preferably, R1, R2 and R3 are independently F or CH3. Preferably, X represents a C1 to C4 alkylene group, and more preferably a C2 or a C3 alkylene group. Preferably, m is 0 to 10, or 0 to 5, or 0 to 2. More preferably, Y is a covalent bond (i.e., m = 0). Preferably, R4 represents a cyano group (-CN). Within the general formula (I), the silane solvent may have one of the more particular formulas (II) or (III) or (IV) or (V) below: R1 (OC1-12C1-12 02 rs ## STR2 ## wherein R 1 is R 1, R 1, R 1, R 1, R 1, R 1, R 1, R 1, R 1, R 1, R 1, R 1, R 3 or R 3. In these formulas (II) to (V), n, m, R 1, R 2, R 3 and R 4 have the same meanings (and the same preferred meanings) as above. Preferably, in these formulas (II) to (V), n is greater than or equal to 1 and m is greater than or equal to 1.
    [0012] Preferred compounds for the silane solvent are: 4- (trimethylsilyl) butanenitrile; 4- (fluorodimethylsilyl) butanenitrile; 4- (difluoromethylsilyl) butanenitrile; 4- (trifluorosilyl) butanenitrile; 3- (trimethylsilyl) butanenitrile; 3- (fluorodimethylsilyl) butanenitrile; 3- (difluoromethylsilyl) butanenitrile; 3- (trifluorosilyl) butanenitrile; 3- (trimethylsilyl) propanenitrile; 3- (fluorodimethylsilyl) propanenitrile; 3- (difluoromethylsilyl) propanenitrile; and 3- (trifluorosilyl) propanenitrile. 4- (Fluorodimethylsilyl) butanenitrile is most preferred. This compound has the formula (IIIa): ## STR2 ## Combinations of two or more of the above silane solvents can be used. The silane solvents above can be manufactured as described in US 2014/0356735.
    [0013] The silane solvent is preferably employed in combination with another solvent, for example a mixture of organic carbonates. Preferably, the other solvent is predominant in volume relative to the silane solvent.
    [0014] The silane solvent may for example represent from 0.5 to 5% by weight relative to the total of the composition, in particular from 1 to 4% by weight. A battery or accumulator according to the invention comprises at least one cathode, an anode, and an electrolyte interposed between the cathode and the anode. The terms cathode and anode are given with reference to the discharge mode of the battery. According to one embodiment, the battery has several cells, each comprising a cathode, an anode, and an electrolyte interposed between the cathode and the anode. In this case, preferably, all the cells are as described above in the summary of the invention. Furthermore, the invention also relates to an individual cell having a cathode, an anode and an electrolyte, the cathode and the electrolyte being as described above in the summary of the invention. The cathode comprises an active material. By "active material" is meant a material in which the lithium ions from the electrolyte are capable of being inserted, and from which the lithium ions are capable of being released into the electrolyte. In addition to the active material, the cathode may advantageously comprise: an electronic conductive additive; and / or - a polymeric binder.
    [0015] The cathode may be in the form of a composite material comprising the active material, the polymeric binder and the electronically conductive additive. The electronically conductive additive may for example be an allotropic form of carbon. As an electronic conductor, there may be mentioned carbon black, SP carbon, carbon nanotubes and carbon fibers. The polymeric binder may be, for example, a fluorinated functionalized or nonfunctional polymer, such as poly (difluorovinyl), or an aqueous-based polymer, for example carboxymethylcellulose or a styrene-butadiene latex. The cathode may comprise a metal current collector on which the composite material is deposited. This current collector can in particular be made of aluminum.
    [0016] The manufacture of the cathode can be carried out as follows. All the compounds mentioned above are dissolved in an organic or aqueous solvent to form an ink. The ink is homogenized, for example using an ultra thurax. This ink is then rolled onto the current collector, the solvent is removed by drying. The anode may for example comprise lithium metal, graphite, carbon, carbon fibers, a Li4Ti5012 alloy or a combination thereof. The composition and method of preparation are similar to those of the cathode, with the exception of the active ingredient.
    [0017] EXAMPLES The following examples illustrate the invention without limiting it. EXAMPLE 1 Electrolyte Based on LiFSI An electrolyte according to the invention is prepared by dissolving LiFSI at a room temperature of 1 mol / l in a mixture of ethylene carbonate and diethyl carbonate in volumetric proportions of 3 and 7 respectively. To this mixture, the solvent of formula (111a) above is added in a mass proportion of 2% relative to the total weight of the electrolyte. A second (comparative) electrolyte is made in the manner but without the solvent of formula (IIIa). The passivation of the aluminum of these two electrolytes is studied in a CR2032 button cell, with aluminum foil at the cathode and lithium metal as reference to the anode. A fiberglass separator is impregnated with the electrolyte of interest. A voltage sweep between 2 and 5.5 V is applied to the button cell with a scanning speed of 0.1 mV / s and the oxidation current is detected. Figure 1 illustrates the effect of the addition of the silane solvent on the corrosion of aluminum. It is found that the silane solvent reduces the corrosion of aluminum.
    [0018] Example 2 - LiTDI Electrolyte An electrolyte according to the invention was made by dissolving LiTDI at a room temperature at a concentration of 1 mol / L in a mixture of ethylene carbonate and diethyl carbonate in volumetric proportions of 3% and 3% respectively. 7. To this mixture, the solvent of formula (111a) above is added in a mass proportion of 2% relative to the total weight of the electrolyte. A second electrolyte (comparative) is made in the manner but without the solvent of formula (IIIa). The SEI formation of these two electrolytes is studied in a CR2032 button cell with a graphite electrode deposited on copper at the cathode, and lithium metal as a reference to the anode. A fiberglass separator is impregnated with the studied electrolyte. Each button cell undergoes two charge-discharge phases at a C / 24 rate (i.e. a charge or discharge in 24 hours). For this, a negative current is applied during the charging, and a positive current is applied during the discharge. The irreversible capacitance is determined by making the difference in capacitance between the first and second charges. This irreversible capacity is: - 21% with the comparative electrolyte without solvent silane; and - 15% with the electrolyte of the invention with silane solvent. As a result, the capacity of the Li-ion battery is increased by 6% by adding the silane solvent into the electrolyte.
    权利要求:
    Claims (12)
    [0001]
    REVENDICATIONS1. An electrolyte composition comprising: - a lithium bis (fluorosulfonyl) imide salt and / or a salt of
    [0002]
    2- lithium trifluoromethyl-4,5-dicyanoimidazolate; and a solvent of formula (I) in which: n is an integer ranging from 0 to 15, - R1, R2 and R3 independently represent a halogen atom or an alkyl group; linear or branched C1 to C6, - X represents either a covalent bond or a linear or branched C1 to C6 alkylene, alkenylene or alkynylene group, - Y represents either a group - (OCH2CH2), - or a group - (N (CH3) CH2CH2) m-, where m is an integer from 0 to 15 with the proviso that m is other than 0 when X is a covalent bond, and - R4 is cyano, cyanate, isocyanate, thiocyanate or isothiocyanate. 2. The composition according to claim 1, wherein the solvent of formula (I) is more precisely of formula (II): ## STR2 ## in which: n and m are integers being from 1 to 15, R 1, R 2 and R 3 independently represent a halogen atom or a linear or branched C 1 to C 6 alkyl group, and R 4 represents a cyano, cyanate, isocyanate group , thiocyanate or isothiocyanate.
    [0003]
    3. Composition according to claim 1, wherein the solvent of formula (I) is more precisely of formula (III): in which: X represents either a covalent bond or a linear or branched alkylene, alkenylene or alkynylene group at C6, - R1, R2 and R3 independently represent a halogen atom or a linear or branched C1-C6 alkyl group, and - R4 represents a cyano, cyanate, isocyanate, thiocyanate or isothiocyanate group.
    [0004]
    4. Composition according to claim 1, wherein the solvent of formula (I) is more precisely of formula (IV): (IV) CH3 NCH2CH2 D4 wherein: - X represents either a covalent bond or an alkylene, alkenylene or alkynylene group linear or branched C1 to C6, m represents an integer from 1 to 15, - R1, R2 and R3 independently represent a halogen atom or a linear or branched C1 to C6 alkyl group, and - R4 represents a cyano, cyanate, isocyanate, thiocyanate or isothiocyanate group. 3033945 15
    [0005]
    5. Composition according to claim 1, wherein the solvent of formula (1) is more precisely of formula (V): (V) OCH 2 CH 2) mR 4 in which: X represents either a covalent bond or an alkylene, alkenylene or C1-C6 linear or branched alkynylene; m is an integer from 1 to 15; R1, R2 and R3 independently represent a halogen atom or a linear or branched C1-C6 alkyl group; and R4 represents a cyano, cyanate, isocyanate, thiocyanate or isothiocyanate group.
    [0006]
    The composition according to claim 1, wherein the solvent of formula (1) is more precisely of formula (IIIa): (iiia) H3c-si-C3H6-CN
    [0007]
    7. Composition according to one of claims 1 to 6, wherein the mass concentration of lithium bis (fluorosulfonyl) imide salt and / or lithium 2-trifluoromethyl-4,5-dicyanoimidazolate salt in the composition. is from 0.5 to 16%.
    [0008]
    8. Composition according to one of claims 1 to 7, wherein the mass concentration of solvent of formula (1) in the composition is 0.5 to 5%.
    [0009]
    9. Composition according to one of claims 1 to 8, also comprising at least one additional solvent, and preferably a mixture of two or three additional solvents, chosen from carbonates, glymes, nitriles, dinitriles, fluorinated solvents, and combinations thereof; the composition more preferably comprising a mixture of carbonates, such as a mixture of ethylene carbonate and diethyl carbonate.
    [0010]
    10. Composition according to one of claims 1 to 9, comprising another lithium salt, preferably selected from the salts LiPF6, LiBF4, CH3COOLi, CH3SO3Li, CF3SO3Li, CF3COOLi, Li2B12F12 and LiBC40a.
    [0011]
    11. Composition according to one of claims 1 to 10, wherein the mass concentration of other lithium salt is less than or equal to 15.5%.
    [0012]
    12. Battery comprising at least one cell which comprises a cathode, an anode and the electrolyte composition according to one of claims 1 to 11, interposed between the cathode and the anode. 20
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    CN109935908B|2019-04-02|2022-02-08|合肥工业大学|Low-concentration lithium salt electrolyte and lithium secondary battery comprising same|
    EP3951989A1|2019-11-07|2022-02-09|Lg Energy Solution, Ltd.|Non-aqueous electrolyte solution for lithium secondary battery and lithium secondary battery comprising same|
    WO2021226483A1|2020-05-07|2021-11-11|Fastcap Systems Corporation|Wide temperature electrolyte|
    CN112271336B|2020-11-25|2021-08-27|广州天赐高新材料股份有限公司|Electrolyte and lithium secondary battery|
    法律状态:
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    优先权:
    申请号 | 申请日 | 专利标题
    FR1552122A|FR3033945B1|2015-03-16|2015-03-16|ELECTROLYTE FORMULATION FOR LITHIUM-ION BATTERIES|FR1552122A| FR3033945B1|2015-03-16|2015-03-16|ELECTROLYTE FORMULATION FOR LITHIUM-ION BATTERIES|
    PL16711883T| PL3271963T3|2015-03-16|2016-03-14|Electrolyte formulation for lithium-ion batteries|
    US15/551,446| US20180034106A1|2015-03-16|2016-03-14|Electrolyte formulation for lithium-ion batteries|
    HUE16711883A| HUE041197T2|2015-03-16|2016-03-14|Electrolyte formulation for lithium-ion batteries|
    PCT/FR2016/050559| WO2016146925A1|2015-03-16|2016-03-14|Electrolyte formulation for lithium-ion batteries|
    KR1020177022912A| KR20170128238A|2015-03-16|2016-03-14|Electrolyte formulation for lithium-ion batteries|
    JP2017548471A| JP2018508112A|2015-03-16|2016-03-14|Electrolyte blending composition for lithium ion battery|
    CN201680012839.4A| CN107408727A|2015-03-16|2016-03-14|Electrolyte formulation for lithium ion battery|
    EP16711883.5A| EP3271963B1|2015-03-16|2016-03-14|Electrolyte formulation for lithium-ion batteries|
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