Patent Application
20190296395
The present invention relates to cyclic dinitrile compounds of formula (I)
wherein X1, X2, R1, and R2 are defined as described below and to their use in electrolyte compositions and electrochemical cells.
Storing electrical energy is a subject of still growing interest. Efficient storage of electric energy would allow electric energy to be generated when it is advantageous and used when needed. Secondary electrochemical cells are well suited for this purpose due to their reversible conversion of chemical energy into electrical energy and vice versa (rechargeability). Secondary lithium batteries are of special interest for energy storage since they provide high energy density and specific energy due to the small atomic weight of the lithium ion, and the high cell voltages that can be obtained (typically 3 to 5 V) in comparison with other battery systems. For that reason, these systems have become widely used as a power source for many portable electronics such as cellular phones, laptop computers, minicameras, etc.
Secondary lithium batteries like lithium ion batteries typically comprise electrolyte compositions containing one or more organic aprotic solvents, e.g. non-aqueous solvents like organic carbonates, ethers, esters and ionic liquids, at least one conducting salt like LiPF6 and optionally one or more additives for enhancing the performance of electrolyte composition and battery. Useful additives are for example SEI additives, flame retardant additives, water scavenger, overcharge protection additives. A lot of research is ongoing in respect to additives for use in electrolyte compositions to further improve the performance of the electrochemical cell containing the electrolyte composition in many different aspects, e.g. cycle life time, high temperature characteristics, safety, etc.
WO 2015/007554 A1 discloses the use of cyclic dinitriles as additives in electrolyte compositions to obtain lithium secondary ion batteries showing improved capacity retention.
Further aspects of the performance of electrochemical cells are the internal resistance, the increase of internal resistance over the lifetime of the battery, the gas evolution over the life of the battery, and the dissolution of transition metal ions present in the electrode active materials of electrochemical cells. There is still the need for additives for electrolyte compositions leading to improved battery performance, inter alia in respect to the aforementioned aspects. It is in particular desirable if such additives combine more than one favorable property and/or at least do not have a detrimental effect on other properties of the electrochemical cells in which they are used.
It was an object of the present invention to provide compounds suited as additives for electrolyte compositions yielding secondary batteries with improved properties like low gas evolution and low transition metal dissolution from the electrode active materials. A further object of the present invention was to provide secondary batteries of high energy density and/or higher operating voltage having good performance characteristics.
These objects are achieved by compounds of formula (I)
wherein
X1 and X2 are selected independently from each other from N, P and CR3;
R1 and R2 are selected independently from each other from R4, OR4, OSi(R8)3, SR4, S(O)R4,
S(O)2R4, OS(O)2R4, S(O)2OR4, and NR5R6, and in case X1 and X2 are both CR3R1 and R2 may also be selected from F, CN, C(O)OR4, and OC(O)R4,
or R1 and R2 are combined and form together with the C—C bond a 5- to 7-membered cycle, which may be substituted by one or more groups selected from F, CN, R4, OR4, SR4, S(O)R4, S(O)2R4, OS(O)2R4, S(O)2OR4, OSiR83, and NR5R6;
R3 is selected from H, F, CN, R4, OR4, SR4, S(O)R4, S(O)2R4, OS(O)2R4, S(O)2OR4, and NR5R6;
R4 is selected from C1 to C12 alkyl, C3 to C6 (hetero)cycloalkyl, C2 to C12 alkenyl, C2 to C12 alkynyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl, wherein alkyl, (hetero)cycloalkyl, alkenyl, alkynyl, (hetero)aryl, and (hetero)aralkyl may be substituted by one or more substituents selected from F, CN, C(O)OR7, OC(O)R7, OR7, and SR7;
R5 and R6 are selected independently from each other from H, C1 to C12 alkyl, C3 to C6 (hetero)cycloalkyl, C2 to C12 alkenyl, C2 to C12 alkynyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl, wherein alkyl, (hetero)cycloalkyl, alkenyl, alkynyl, (hetero)aryl, and (hetero)aralkyl may be substituted by one or more substituents selected from F and CN;
or R5 and R6 may be combined to form together with the C- or N-atom a 5- to 7-membered heterocycle which may be substituted by one or more substituents selected from F, CN, C1 to C12 alkyl, C3 to C6 (hetero)cycloalkyl, C2 to C12 alkenyl, C2 to C12 alkynyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl, wherein alkyl, (hetero)cycloalkyl, alkenyl, alkynyl, (hetero)aryl, and (hetero)aralkyl may be substituted by one or more substituents selected from F and CN;
R7 is selected from C1 to C12 alkyl, C3 to C6 (hetero)cycloalkyl, C2 to C12 alkenyl, C2 to C12 alkynyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl which may be substituted by one or more substituents selected from F and CN; and
R8 is independently selected from R4 and OR4;
and their use in electrolyte compositions.
The problem is further solved by an electrolyte composition comprising at least one compound of formula (I) and by electrochemical cells comprising said electrolyte composition.
The addition of at least one compound of formula (I) to an electrolyte composition for rechargeable electrochemical cells leads to less gassing, comparably low impedance and may lead to a significant reduction of transition metal dissolution in electrochemical cells.
In the following the invention is described in detail.
One object of the invention are compounds of formula (I)
X1 and X2 are selected independently from each other from N, P and CR3;
R1 and R2 are selected independently from each other from R4, OR4, SR4, S(O)R4, S(O)2R4, OS(O)2R4, S(O)2OR4, OSiR83, and NR5R6, and in case X1 and X2 are both CR3R1 and R2 may also be selected from F, CN, C(O)OR4, and C(O)R4; preferably R1 and R2 are selected independently from each other from R4, OR4, SR4, and NR5R6;
or R1 and R2 are combined and form together with the C—C bond a 5- to 7-membered cycle, which may be substituted by one or more groups selected from F, CN, R4, OR4, SR4, S(O)R4, S(O)2R4, OS(O)2R4, S(O)2OR4, OSiR83, and NR5R6;
R3 is selected from H, F, CN, R4, OR4, SR4, S(O)R4, S(O)2R4, OS(O)2R4, S(O)2OR4, and NR5R6;
R4 is selected from O1 to C12 alkyl, C3 to C6 (hetero)cycloalkyl, C2 to C12 alkenyl, C2 to C12 alkynyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl, wherein alkyl, (hetero)cycloalkyl, alkenyl, alkynyl, (hetero)aryl, and (hetero)aralkyl may be substituted by one or more substituents selected from F, CN, C(O)OR7, C(O)R7, OR7, and SR7;
R5 and R6 are selected independently from each other from H, C1 to C12 alkyl, C3 to C6 (hetero)cycloalkyl, C2 to C12 alkenyl, C2 to C12 alkynyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl, wherein alkyl, (hetero)cycloalkyl, alkenyl, alkynyl, (hetero)aryl, and (hetero)aralkyl may be substituted by one or more substituents selected from F and CN;
or R5 and R6 may be combined to form together with the C- or N-atom a 5- to 7-membered heterocycle which may be substituted by one or more substituents selected from F, CN, C1 to C12 alkyl, C3 to C6 (hetero)cycloalkyl, C2 to C12 alkenyl, C2 to C12 alkynyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl, wherein alkyl, (hetero)cycloalkyl, alkenyl, alkynyl, (hetero)aryl, and (hetero)aralkyl may be substituted by one or more substituents selected from F and CN; R7 is selected from C1 to C12 alkyl, C3 to C6 (hetero)cycloalkyl, C2 to C12 alkenyl, C2 to C12 alkynyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl which may be substituted by one or more substituents selected from F and CN; and R8 is independently selected from R4 and OR4.
The term “C1 to C12 alkyl” as used herein means a straight or branched saturated hydrocarbon group with 1 to 12 carbon atoms having one free valence and wherein one or more CH2-groups may be replaced by O or S, e.g., methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, iso-pentyl, 2,2-dimethylpropyl, n-hexyl, iso-hexyl, 2-ethyl hexyl, n-heptyl, iso-heptyl, n-octyl, iso-octyl, n-nonyl, n-decyl, methoxymethyl, ethoxymethyl, methoxyethyl, and the like. Preferred are C1-C6 alkyl, more preferred are C1-C4alkyl groups and most preferred are methyl, ethyl, and n- and iso-propyl.
The term “C3 to C6 (hetero)cycloalkyl” as used herein means a saturated 3- to 6-membered hydrocarbon cycle having one free valence wherein one or more of the C— atoms of the saturated cycle may be replaced independently from each other by a heteroatom selected from N, S, O and P. Examples of C3 to C6 cycloalkyl include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl, preferred is cyclohexyl. Examples of C3 to C6 hetero cycloalkyl are oxiranyl, tetrahydrofuryl, pyrrolidyl, piperidyl and morpholinyl.
The term “C2 to C12 alkenyl” as used herein refers to an unsaturated straight or branched hydrocarbon group with 2 to 12 carbon atoms having one free valence. Unsaturated means that the alkenyl group contains at least one C═C double bond and wherein one or more CH2-groups may be replaced by O or S. C2 to C12 alkenyl includes for example ethenyl, 1-propenyl, 2-propenyl, 1-n-butenyl, 2-n-butenyl, iso-butenyl, 1-pentenyl, 1-hexenyl, 1-heptenyl, 1-octenyl, 1-nonenyl, 1-decenyl, methoxyethenyl, and the like. Preferred are C2 to C8 alkenyl groups, more preferred are C2 to C6 alkenyl groups, even more preferred are C2 to C4 alkenyl groups and in particular ethenyl and propenyl, the preferred propenyl is 1-propen-3-yl, also called allyl.
The term “C2 to C12 alkynyl” as used herein refers to an unsaturated straight or branched hydrocarbon group with 2 to 12 carbon atoms having one free valence, wherein the hydrocarbon group contains at least one C—C triple bond and wherein one or more CH2-groups may be replaced by O or S. C2 to C10 alkynyl includes for example ethynyl, 1-propynyl, 2-propynyl, 1-n-butinyl, 2-n-butynyl, 1-pentynyl, 1-hexynyl, -heptynyl, 1-octynyl, 1-nonynyl, 1-decynyl, methoxyethynyl, and the like. Preferred are C2 to C10 alkynyl, more preferred are C2 to C6 alkynyl, even more preferred are C2 to C4 alkynyl, in particular preferred are ethynyl and 1-propyn-3-yl (propargyl).
The term “C5 to C12 (hetero)aryl” as used herein denotes an aromatic 5- to 12-membered hydrocarbon cycle or condensed cycles having one free valence wherein one or more of the C— atoms of the aromatic cycle(s) may be replaced independently from each other by a heteroatom selected from N, S, O and P. Examples of C5-C12 (hetero)aryl are pyrrolyl, furanyl, thiophenyl, pyridinyl, pyranyl, thiopyranyl, phenyl, and naphtyl. Preferred is phenyl.
The term “C6 to C24 (hetero)aralkyl” as used herein denotes an aromatic 5- to 12-membered hydrocarbon cycle substituted by one or more C1 to C6 alkyl wherein one or more of the C-atoms of the aromatic cycle may be replaced independently from each other by a heteroatom selected from N, S, O and P and one or more CH2-groups of the alkyl may be substituted by O or S. The C6 to C24 (hetero)aralkyl group contains in total 6 to 24 C— and heteroatoms and has one free valence. The free valence may be located in the aromatic cycle or in a C1 to C6 alkyl group, i.e. C6 to C24 (hetero)aralkyl group may be bound via the (hetero)aromatic part or via the alkyl part of the group. Examples of C6-C24 (hetero)aralkyl are methylphenyl, 2-methylpyridyl, 1,2-dimethylphenyl, 1,3-dimethylphenyl, 1,4-dimethylphenyl, ethylphenyl, 2-propylphenyl, benzyl, CH2-pyridyl, and the like, preferred is benzyl
Preferred compounds of formula (I) are selected from compounds of formula (I) wherein X1 and X2 are independently from each other are selected from N and CR3, more preferred X1 and X2 are either both N or both CR3, most preferred are compounds of formula (I) wherein X1 and X2 are N.
According to another embodiment of the invention X1 and X2 may independently from each other be selected from N and P or X1 and X2 may both be N or may both be P.
In case X, and X2 are both CR3, R1 and R2 may be selected from F, CN, R4, OR4, SR4, S(O)R4, S(O)2R4, OS(O)2R4, S(O)2OR4, OSiR83, NR5R6, C(O)OR4, and OC(O)R4, preferably R1 and R2 are selected from F, CN, R4, OR4, SR4, OSiR83, and NR5R6, and more preferred R1 and R2 are selected from F, CN, OR4, SR4, and NR5R6, and most preferred R1 and R2 are selected from OR4 and SR4, wherein R4 is selected from C5 to C12 (hetero)aryl and C6 to C24 (hetero)aralkyl which may be substituted by one or more substituents selected from F, CN, C(O)OR7, OC(O)R7, OR7, and SR7; or R1 and R2 form together with the C—C bond a 5- to 7-membered unsaturated cycle, which may be substituted by one or more groups selected from F, CN, R4, OR4, SR4, S(O)R4, S(O)2R4, OS(O)2R4, S(O)2OR4, OSiR83, and NR5R6.
In case at least one of X1 and X2 is N or P, R1 and R2 are selected independently from each other from R4, OR4, SR4, S(O)R4, S(O)2R4, OS(O)2R4, S(O)2OR4, OSiR83, and NR5R6; preferably R1 and R2 are selected from R4, OR4, SR4, OSiR83, and NR5R6, and most preferred R1 and R2 are selected from OR4 and SR4, wherein R4 is selected from C1 to C12 alkyl, C5 to C12 (hetero)aryl and C6 to C24 (hetero)aralkyl which may be substituted by one or more substituents selected from F, CN, C(O)OR7, OC(O)R7, OR7, and SR7, preferably R4 is selected from C5 to C12 (hetero)aryl and C6 to C24 (hetero)aralkyl which may be substituted by one or more substituents selected from F, CN, C(O)OR7, OC(O)R7, OR7, and SR7; or R1 and R2 form together with the C—C bond a 5- to 7-membered unsaturated cycle, which may be substituted by one or more groups selected from F, CN, R4, OR4, SR4, S(O)R4, S(O)2R4, OS(O)2R4, S(O)2OR4, OSiR83, and NR5R6.
According to one embodiment of the invention R1 and R2 are selected independently from each other from OR4, SR4, S(O)2R4, OS(O)2R4, S(O)2OR4, OSiR83, and NR5R6, and additionally from F, CN, C(O)OR4, and OC(O)R4, if X, and X2 are both CR3, preferably R1 and R2 are selected independently from each other from OR4, SR4, S(O)2R4, OS(O)2R4, S(O)2OR4, OSiR83, and NR5R6, and more preferred R1 and R2 are selected independently from each other from OR4, SR4, and NR5R6.
According to another embodiment of the invention R1 and R2 are selected independently from each other selected from R4.
It is preferred in any case, that R1 and R2 are equal.
According to a further embodiment of the invention R1 and R2 are combined and form together with the C—C bond a 5- to 7-membered cycle, preferably a 5- to 6-membered cycle which may be substituted by one or more groups selected from F, CN, R4, OR4, SR4, S(O)R4, S(O)2R4, OS(O)2R4, S(O)2OR4, OSiR83, and NR5R6. The 5- to 7-membered cycle contains one or more double bonds and may also be an aromatic cycle. Examples of the 5- to 7-membered unsaturated cycle formed by R1 and R2 together with the C—C bond are cyclopentene, cyclohexene, benzene, and furane.
R4 is selected from C1 to C12 alkyl, C3 to C6 (hetero)cycloalkyl, C2 to C12 alkenyl, C2 to C12 alkynyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl, wherein alkyl, (hetero)cycloalkyl, alkenyl, alkynyl, (hetero)aryl, and (hetero)aralkyl may be substituted by one or more substituents selected from F, CN, C(O)OR7, OC(O)R7, OR7, and SR7; preferably R4 is selected from C1 to C12 alkyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl wherein alkyl, (hetero)aryl, and hetero(aralkyl) may be substituted by one or more substituents selected from F, CN, C(O)OR7, OC(O)R7, OR7, and SR7.
R5 and R6 are selected independently from each other from H, C1 to C12 alkyl, C3 to C6 (hetero)cycloalkyl, C2 to C12 alkenyl, C2 to C12 alkynyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl, wherein alkyl, (hetero)cycloalkyl, alkenyl, alkynyl, (hetero)aryl, and (hetero)aralkyl may be substituted by one or more substituents selected from F and CN; preferably R5 and R6 are selected independently from each other from H, C1 to C12 alkyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl which may be substituted by one or more substituents selected from F and CN;
or R5 and R6 may be combined to form together with the C- or N-atom a 5- to 7-membered heterocycle which may be substituted by one or more substituents selected from F, CN, C1 to C12 alkyl, C3 to C6 (hetero)cycloalkyl, C2 to C12 alkenyl, C2 to C12 alkynyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl, wherein alkyl, (hetero)cycloalkyl, alkenyl, alkynyl, (hetero)aryl, and (hetero)aralkyl may be substituted by one or more substituents selected from F and CN; preferably 5- to 7-membered heterocycle may be substituted by F, CN, and C1 to C12 alkyl.
R7 is selected from C1 to C12 alkyl, C3 to C6 (hetero)cycloalkyl, C2 to C12 alkenyl, C2 to C12 alkynyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl which may be substituted by one or more substituents selected from F and CN, preferably R7 is selected from C1 to C12 alkyl, which may be substituted by one or more substituents selected from F and CN.
R8 is independently selected from R4 and OR4, e.g. in the group OSiR83 all R8 may be OR4, or all R8 may be R4 or OSiR83 may contain both OR4 and R4. Preferably R8 is selected from OC1 to C12 alkyl and C1 to C12 alkyl, most preferred R8 is selected from OC1 to C12 alkyl.
Preferred compounds of formula (I) are compounds of formula (I) wherein
X1 and X2 are N,
R1 and R2 are selected independently from each other from R4, OR4, and SR7, preferably from OR4, and SR7, and
R4 is selected from C1 to C12 alkyl, C5 to C12 (hetero)aryl, and C6 to C24 (hetero)aralkyl wherein alkyl, (hetero)aryl, and hetero(aralkyl) may be substituted by one or more substituents selected from F and CN.
Examples of compounds of formula (I) are compounds of formula
(I.a) X1 and X2 are N and R1 and R2 are O—CH2-phenyl or O—CH2—CF3,
(I.b) X1 and X2 are N and R1 and R2 are S-phenyl or S—CH2-Phenyl,
(I.c) X1 and X2 are N and R1 and R2 are phenyl or ethynyl, and
(I.d) X1 and X2 are N and R1 and R2 are OCH3.
The preparation of the compounds of formula (I) is known to the person skilled in the art. For example they may be prepared by reacting diaminonitrile with R1C(O)C(O)R2, or by reacting 5,6-dichloro-2,3-dicyanopyrazine with the respective nucleophiles Nu1-R1 and Nu2-R2.
The reaction of diaminonitrile with R1C(O)C(O)R2 is a condensation reaction according to scheme (a):
The reaction of 5,6-dichloro-2,3-dicyanopyrazine with nucleophiles like alcohols, thiols, amine, organometallic reagents etc. follows scheme (b):
Nu1-R1 and Nu2-R2 are the nucleophilic derivatives of R1 and R2, respectively, which allow the reaction with the aromatic dichloro compound to yield the cyclic dinitriles of formula (I). E.g.
Nu1-R1 and Nut-R2 may be selected from R4OH, R4SH, HNR5R6, R4—S(O)2—OH, R4—S(O)2—OM (M=Li, Na, K), and nucleophiles functionalized by an organometallic groups M*-R1 and M*-R2 like Aryl-MgBr or Aryl-MgCl, vinyl-MgBr, ethynyl-MgBr. Compounds of formula (I) wherein R1 and/or R2 are selected from S(O)2OR4 may be prepared by oxidation of the reaction product of R4SH with the dichloro compound. The preparation of the compounds of formula (I) described herein is also an object of the present invention.
According to another object of the invention the compounds of formula (I), as described above or as described as being preferred, are used in electrolyte compositions for electrochemical cells. It is preferred to use the compounds of formula (I) in non-aqueous electrolyte compositions, more preferred the compounds of formula (I) are used in electrolyte compositions for lithium batteries, even more preferred in electrolyte compositions for lithium ion batteries.
Accordingly, when a compound of formula (I) is used in an electrolyte composition, the total concentration of the compound(s) of formula (I) in the electrolyte composition is typically 0.005 to 10 wt.-%, preferred 0.01 to 5 wt.-% and most preferred 0.05 to 2 wt.-%, based on the total weight of the electrolyte composition. Usually the compound(s) of formula (I) are added to the electrolyte composition in the desired amount during or after manufacture of the electrolyte composition.
A further object of the invention is an electrolyte composition containing at least one compound of formula (I). The minimum total concentration of compounds of formula (I) in the electrolyte composition is usually 0.005 wt.-%, typically the total concentration of compound(s) of formula (I) in the electrolyte composition is 0.005 to 10 wt.-%, preferred 0.01 to 5 wt.-% and most preferred 0.05 to 2 wt.-%, based on the total weight of the electrolyte composition. The term “wt.-%” as used herein means percent by weight.
The electrolyte composition preferably contains at least one aprotic organic solvent, more preferred at least two aprotic organic solvents. According to one embodiment the electrolyte composition may contain up to ten aprotic organic solvents.
The at least one aprotic organic solvent is preferably selected from cyclic and acyclic organic carbonates, di-C1-C10-alkylethers, di-C1-C4-alkyl-C2-C6-alkylene ethers and polyethers, cyclic ethers, cyclic and acyclic acetales and ketales, orthocarboxylic acids esters, cyclic and acyclic esters of carboxylic acids, cyclic and acyclic sulfones, and cyclic and acyclic nitriles and dinitriles.
More preferred the at least one aprotic organic solvent is selected from cyclic and acyclic carbonates, di-C1-C10-alkylethers, di-C1-C4-alkyl-C2-C6-alkylene ethers and polyethers, cyclic and acyclic acetales and ketales, and cyclic and acyclic esters of carboxylic acids, even more preferred the electrolyte composition contains at least one aprotic organic solvent selected from cyclic and acyclic carbonates, and most preferred the electrolyte composition contains at least two aprotic organic solvents selected from cyclic and acyclic carbonates, in particular preferred the electrolyte composition contains at least one aprotic solvent selected from cyclic carbonates and at least one aprotic organic solvent selected from acyclic carbonates.
The aprotic organic solvents may be partly halogenated, e.g. they may be partly fluorinated, partly chlorinated or partly brominated, and preferably they may be partly fluorinated. “Partly halogenated” means, that one or more H of the respective molecule is substituted by a halogen atom, e.g. by F, Cl or Br. Preference is given to the substitution by F. The at least one solvent may be selected from partly halogenated and non-halogenated aprotic organic solvents i.e. the electrolyte composition may contain a mixture of partly halogenated and non-halogenated aprotic organic solvents.
Examples of cyclic carbonates are ethylene carbonate (EC), propylene carbonate (PC) and butylene carbonate (BC), wherein one or more H of the alkylene chain may be substituted by F and/or an C1 to C4 alkyl group, e.g. 4-methyl ethylene carbonate, monofluoroethylene carbonate (FEC), and cis- and trans-difluoroethylene carbonate. Preferred cyclic carbonates are ethylene carbonate, monofluoroethylene carbonate and propylene carbonate, in particular ethylene carbonate.
Examples of acyclic carbonates are di-C1-C10-alkylcarbonates, wherein each alkyl group is selected independently from each other, preferred are di-C1-C4-alkylcarbonates. Examples are e.g. diethyl carbonate (DEC), ethyl methyl carbonate (EMC), dimethyl carbonate (DMC), and methylpropyl carbonate. Preferred acyclic carbonates are diethyl carbonate (DEC), ethyl methyl carbonate (EMC), dimethyl carbonate (DMC).
In one embodiment of the invention the electrolyte composition contains mixtures of acyclic oganic carbonates and cyclic organic carbonates at a ratio by weight of from 1:10 to 10:1, preferred of from 5:1 to 1:5.
According to the invention each alkyl group of the di-C1-C10-alkylethers is selected independently from the other. Examples of di-C1-C10-alkylethers are dimethylether, ethyl-methylether, diethylether, methylpropylether, diisopropylether, and di-n-butylether.
Examples of di-C1-C4-alkyl-C2-C6-alkylene ethers are 1,2-dimethoxyethane, 1,2-diethoxyethane, diglyme (diethylene glycol dimethyl ether), triglyme (triethyleneglycol dimethyl ether), tetraglyme (tetraethyleneglycol dimethyl ether), and diethylenglycoldiethylether.
Examples of suitable polyethers are polyalkylene glycols, preferably poly-C1-C4-alkylene glycols and especially polyethylene glycols. Polyethylene glycols may comprise up to 20 mol % of one or more C1-C4-alkylene glycols in copolymerized form. Polyalkylene glycols are preferably dimethyl- or diethyl-end-capped polyalkylene glycols. The molecular weight Mw of suitable polyalkylene glycols and especially of suitable polyethylene glycols may be at least 400 g/mol. The molecular weight Mw of suitable polyalkylene glycols and especially of suitable polyethylene glycols may be up to 5 000 000 g/mol, preferably up to 2 000 000 g/mol.
Examples of cyclic ethers are 1,4-dioxane, tetrahydrofuran, and their derivatives like 2-methyl tetrahydrofuran.
Examples of acyclic acetals are 1,1-dimethoxymethane and 1,1-diethoxymethane. Examples of cyclic acetals are 1,3-dioxane, 1,3-dioxolane, and their derivatives such as methyl dioxolane.
Examples of acyclic orthocarboxylic acid esters are tri-C1-C4 alkoxy methane, in particular trimethoxymethane and triethoxymethane. Examples of suitable cyclic orthocarboxylic acid esters are 1,4-dimethyl-3,5,8-trioxabicyclo[2.2.2]octane and 4-ethyl-1-methyl-3,5,8-trioxabicyclo[2.2.2]octane.
Examples of acyclic esters of carboxylic acids are ethyl and methyl formiate, ethyl and methyl acetate, ethyl and methyl proprionate, and ethyl and methyl butanoate, and esters of dicarboxylic acids like 1,3-dimethyl propanedioate. An example of a cyclic ester of carboxylic acids (lactones) is γ-butyrolactone.
Examples of cyclic and acyclic sulfones are ethyl methyl sulfone, dimethyl sulfone, and tetrahydrothiophene-S,S-dioxide (sulfolane).
Examples of cyclic and acyclic nitriles and dinitriles are adipodinitrile, acetonitrile, propionitrile, and butyronitrile.
The inventive electrolyte composition usually contains at least one conducting salt. The electrolyte composition functions as a medium that transfers ions participating in the electrochemical reaction taking place in an electrochemical cell. The conducting salt(s) present in the electrolyte are usually solvated in the aprotic organic solvent(s). Preferably the conducting salt is a lithium conducting salt. The conducting salt is preferably selected from the group consisting of
Suited 1,2- and 1,3-diols from which the bivalent group (ORIIO) is derived may be aliphatic or aromatic and may be selected, e.g., from 1,2-dihydroxybenzene, propane-1,2-diol, butane-1,2-diol, propane-1,3-diol, butan-1,3-diol, cyclohexyl-trans-1,2-diol and naphthalene-2,3-diol which are optionally are substituted by one or more F and/or by at least one straight or branched non fluorinated, partly fluorinated or fully fluorinated C1-C4 alkyl group. An example for such 1,2- or 1,3-diole is 1,1,2,2-tetra(trifluoromethyl)-1,2-ethane diol.
“Fully fluorinated C1-C4 alkyl group” means, that all H-atoms of the alkyl group are substituted by F.
Suited 1,2- or 1,3-dicarboxlic acids from which the bivalent group (ORIIO) is derived may be aliphatic or aromatic, for example oxalic acid, malonic acid (propane-1,3-dicarboxylic acid), phthalic acid or isophthalic acid, preferred is oxalic acid. The 1,2- or 1,3-dicarboxlic acid are optionally substituted by one or more F and/or by at least one straight or branched non fluorinated, partly fluorinated or fully fluorinated C1-C4 alkyl group.
Suited 1,2- or 1,3-hydroxycarboxylic acids from which the bivalent group (ORIIO) is derived may be aliphatic or aromatic, for example salicylic acid, tetrahydro salicylic acid, malic acid, and 2-hydroxy acetic acid, which are optionally substituted by one or more F and/or by at least one straight or branched non fluorinated, partly fluorinated or fully fluorinated C1-C4 alkyl group. An example for such 1,2- or 1,3-hydroxycarboxylic acids is 2,2-bis(trifluoromethyl)-2-hydroxy-acetic acid.
Examples of Li[B(RI)4], Li[B(RI)2(ORIIO)] and Li[B(ORIIO)2] are LiBF4, lithium difluoro oxalato borate and lithium dioxalato borate.
Preferably the at least one conducting salt (ii) is selected from Li[N(FSO2)2], Li[N(CF3SO2)2], LiClO4, LiPF6, LiBF4, and LiPF3(CF2CF3)3, more preferred the conducting salt (ii) is selected from LiPF6 and LiBF4, and the most preferred conducting salt (ii) is LiPF6.
The at least one conducting salt is usually present at a minimum concentration of at least 0.1 mol/I, preferably the concentration of the at least one conducting salt is 0.5 to 2 mol/1 based on the entire electrolyte composition.
The electrolyte composition according to the present invention may contain at least one further additive different from the compounds of formula (I) and formula (II). The further additive may be selected from polymers, SEI forming additives, flame retardants, overcharge protection additives, wetting agents, HF and/or H2O scavenger, stabilizer for LiPF6 salt, ionic solvation enhancer, corrosion inhibitors, gelling agents, and the like.
Examples for polymers used in electrolyte compositions are polyvinylidene fluoride, polyvinylidene-hexafluoropropylene copolymers, polyvinylidene-hexafluoropropylenech lorotrifluoroethylene copolymers, Nafion, polyethylene oxide, polymethyl methacrylate, polyacrylonitrile, polypropylene, polystyrene, polybutadiene, polyethylene glycol, polyvinylpyrrolidone, polyaniline, polypyrrole and/or polythiophene. These polymers may be added to electrolyte compositions containing a solvent or solvent mixture in order to convert liquid electrolytes into quasi-solid or solid electrolytes and thus to improve solvent retention, especially during ageing.
Examples of flame retardants are organic phosphorous compounds like cyclophosphazenes, phosphoramides, alkyl and/or aryl tri-substituted phosphates, alkyl and/or aryl di- or tri-substituted phosphites, alkyl and/or aryl di-substituted phosphonates, alkyl and/or aryl tri-substituted phosphines, and fluorinated derivatives thereof.
Examples of HF and/or H2O scavenger are optionally halogenated cyclic and acyclic silylamines.
Examples of overcharge protection additives are cyclohexylbenzene, o-terphenyl, p-terphenyl, and biphenyl and the like, preferred are cyclohexylbenzene and biphenyl.
Examples of SEI forming additives are vinylene carbonate and its derivatives such as vinylene carbonate and methylvinylene carbonate; fluorinated ethylene carbonate and its derivatives such as monofluoroethylene carbonate, cis- and trans-difluorocarbonate; propane sultone and its derivatives; ethylene sulfite and its derivatives; oxalate comprising compounds such as lithium oxalate, oxalato borates including dimethyl oxalate, lithium bis(oxalate) borate, lithium difluoro (oxalato) borate, and ammonium bis(oxalato) borate, and oxalato phosphates including lithium tetrafluoro (oxalato) phosphate; lithium fluorophosphates including LiPO2F2; and ionic compounds of formula (II) K+A− containing a cation K+ of formula (IIa)
wherein
X is CH2 or NRc,
Ra is selected from C1 to C6 alkyl,
Rb is selected from —(CH2)—SO3—(CH2)v—Rd,
—SO3— is —O—S(O)2— or —S(O)2—O—, preferably —SO3— is —O—S(O)2—,
u is an integer from 1 to 8, preferably u is 2, 3 or 4, wherein one or more CH2 groups of the —(CH2)— alkylene chain which are not directly bound to the N-atom and/or the SO3 group may be replaced by O and wherein two adjacent CH2 groups of the —(CH2)u— alkylene chain may be replaced by a C═C double bond, preferably the —(CH2)u— alkylene chain is not substituted and u u is an integer from 1 to 8, preferably u is 2, 3 or 4,
v is an integer from 1 to 4, preferably v is 0,
Rc is selected from C1 to C6 alkyl,
Rd is selected from C1-C20 alkyl, C2-C20 alkenyl, C2-C20 alkynyl, C6-C12 aryl, and C6-C24 aralkyl, which may contain one or more F, and wherein one or more CH2 groups of alkyl, alkenyl, alkynyl and aralkyl which are not directly bound to the SO3 group may be replaced by O, preferably Rb is selected from C1-C6 alkyl, C2-C4 alkenyl, and C2-C4 alkynyl, which may contain one or more F, and wherein one or more CH2 groups of alkyl, alkenyl, alkynyl and aralkyl which are not directly bound to the SO3 group may be replaced by O, preferred examples of Rb include methyl, ethyl, trifluoromethyl, pentafluoroethyl, n-propyl, n-butyl, n-hexyl, ethenyl, ethynyl, allyl or prop-1-yn-yl,
and an anion A− selected from bisoxalato borate, difluoro (oxalato) borate, [FzB(CmF2m+1)4-z]−, [FyP(CmF2m+1)6-y]−, [(CmF2m+1)2P(O)O]−, [CmF2m+1P(O)O2]2−, [O—C(O)—CmF2m+1]−, [O—S(O)2-CmF2m+1]−, [N(C(O)—CmF2m+1)2]—, [N(S(O)2—CmF2m+1)2]—, [N(C(O)—CmF2m+1)(S(O)2—CmF2m+1)]—, [N(C(O)—CmF2m+1)(C(O)F)]−, [N(S(O)2—CmF2m+1)(S(O)2F)]−, [N(S(O)2F)2]−, [C(C(O)—CmF2m+1)3]—, [C(S(O)2—CmF2m+1)3]−, wherein m is an integer from 1 to 8, z is an integer from 1 to 4, and y is an integer from 1 to 6,
Preferred anions A− are bisoxalato borate, difluoro (oxalato) borate, [F3B(CF3)]−, [F3B(C2F5)]−, [PF6]−, [F3P(C2F5)3]−, [F3P(C3F7)3]−, [F3P(C4F9)3]−, [F4P(C2F5)2]−, [F4P(C3F7)2]−, [F4P(C4F9)2]−, [F5P(C2F5)]−, [F5P(C3F7)] or [F5P(C4F9)]−, [(C2F5)2P(O)O]−, [(C3F7)2P(O)O]− or [(C4F9)2P(O)O]−, [C2F5P(O)O2]2−, [C3F7P(O)O2]2−, [C4F9P(O)O2]2−, [O—C(O)CF3]−, [O—C(O)C2F5]−, [O—C(O)C4F9]−, [C—S(O)2CF3]−, [O—S(O)2C2F5]−, [N(C(O)C2F5)2]−, [N(O(O)(CF3)2]−, [N(S(O)2CF3)2]−, [N(S(O)2C2F5)2]−, [N(S(O)2C3F7)2]−, [N(S(O)2CF3) (S(O)2C2F5)]−, [N(S(O)2C4F9)2]−, [N(C(O)CF3)(S(O)2CF3)]−, [N(C(O)C2F5)(S(O)2CF3)] or [N(C(O)CF3)(S(O)2—C4F9)]−, [N(C(O)CF3)(C(O)F)]−, [N(C(O)C2F5)(C(O)F)]−, [N(C(O)C3F7)(C(O)F)]−, [N(S(O)2CF3)(S(O)2F)]−, [N(S(O)2C2F5)(S(O)2F)], [N(S(O)2C4F9)(S(O)2F)], [C(C(O)CF3)3]−, [C(C(O)C2F5)3] or [C(C(O)C3F7)3]−, [C(S(O)2CF3)3]−, [C(S(O)2C2F5)3]−, and [C(S(O)2C4F9)3]−.
More preferred the anion is selected from bisoxalato borate, difluoro (oxalato) borate, CF3SO3−, and [PF3(C2F5)3]− Compounds of formula (II) and their preparation are described in WO 2013/026854 A1.
Preferred SEI-forming additives are oxalato borates, fluorinated ethylene carbonate and its derivatives, vinylene carbonate and its derivatives, and compounds of formula (II). More preferred are lithium bis(oxalato) borate (LiBOB), lithium difluoro(oxalato) borate (LidFOB), lithium fluorophosphates (e.g. LiPO2F2) vinylene carbonate, monofluoro ethylene carbonate, and compounds of formula (II), in particular monofluoro ethylene carbonate, and compounds of formula (II).
A compound added as additive may have more than one effect in the electrolyte composition and the device comprising the electrolyte composition. E.g. lithium oxalato borate may be added as additive enhancing the SEI formation but it may also be added as conducting salt.
In case one or more further additives are present, the total concentration of all further additives is at least 0.05 wt.-%, based on the total amount of the electrolyte composition, preferred the total concentration of the one or more further additives is 0.1 to 30 wt.-%, more preferred 0.5 to 10 wt.-%.
According to one embodiment of the present invention the electrolyte composition contains at least one compound of formula (I) and at least one SEI forming additive, all as described above or as described as being preferred.
In one embodiment of the present invention, the electrolyte composition contains:
The electrolyte composition preferably contains
The inventive electrolyte composition is preferably liquid at working conditions; more preferred it is liquid at 1 bar and 25° C., even more preferred the electrolyte composition is liquid at 1 bar and −15° C.
The water content of the inventive electrolyte composition is preferably below 100 ppm, based on the weight of the electrolyte composition, more preferred below 50 ppm, most preferred below 30 ppm. The water content may be determined by titration according to Karl Fischer, e.g. described in detail in DIN 51777 or ISO760: 1978.
The content of HF of the inventive electrolyte composition is preferably below 200 ppm, based on the weight of the electrolyte composition, more preferred below 100 ppm, most preferred below 60 ppm. The HF content may be determined by titration according to potentiometric or potentiographic titration method.
The electrolyte compositions of the invention are prepared by methods which are known to the person skilled in the field of the production of electrolytes, generally by dissolving a conductiing salt in the corresponding solvent mixture and adding the compound(s) of the formula (I) according to the invention and optionally additional additives, as described above.
The electrolyte compositions are used in electrochemical cells like secondary lithium batteries, double layer capacitors, and lithium ion capacitors, preferably the inventive electrolyte compositions are used in secondary lithium batteries and more preferred in lithium ion batteries.
Another object of the present invention is an electrochemical cell comprising the electrolyte composition as described above.
The general construction of such electrochemical devices is known and is familiar to the person skilled in this art for batteries, for example, in Linden's Handbook of Batteries (ISBN 978-0-07-162421-3).
The inventive electrochemical cell may be a secondary lithium battery, a double layer capacitor, or a lithium ion capacitor. Preferably the electrochemical cell is a secondary lithium battery. The term “secondary lithium battery” as used herein means a secondary electrochemical cell, wherein the anode comprises lithium metal or lithium ions sometime during the charge/discharge of the cell. The anode may comprise lithium metal or a lithium metal alloy, a material occluding and releasing lithium ions, or other lithium containing compounds; e.g. the lithium battery may be a lithium ion battery, a lithium/sulphur battery, or a lithium/selenium sulphur battery.
In particular preferred the electrochemical device is a lithium ion battery, i.e. a secondary lithium ion electrochemical cell comprising a cathode comprising a cathode active material that can reversibly occlude and release lithium ions and an anode comprising an anode active material that can reversibly occlude and release lithium ions. The terms “secondary lithium ion electrochemical cell” and “(secondary) lithium ion battery” are used interchangeably within the present invention.
The at least one cathode active material preferably comprises a material capable of occluding and releasing lithium ions selected from lithium transition metal phosphates and lithium intercalating metal oxides. The lithium is usually intercalated in form of lithium ions.
Examples of lithium transition metal phosphates are LiFePO4 and LiCoPO4, examples of lithium intercalating metal oxides are LiCoO2, LiNiO2, mixed transition metal oxides with layer structure having the general formula Li(1+z)[NiaCobMnc](1-z)O2+e wherein z is 0 to 0.3; a, b and c may be same or different and are independently 0 to 0.8 wherein a+b+c=1; and −0.1≤e≤0.1, and manganese-containing spinels like LiMnO4 and spinels of general formula Li1+tM2-tO4-d wherein d is 0 to 0.4, t is 0 to 0.4 and M is Mn and at least one further metal selected from the group consisting of Co and Ni, and Li(1+g)[NihCoiAlj](1-g)O2+k. Typical values for g, h, l, j and k are: g=0, h=0.8 to 0.85, i=0.15 to 0.20, j=0.02 to 0.03 and k=0.
The cathode may further comprise electrically conductive materials like electrically conductive carbon and usual components like binders. Compounds suited as electrically conductive materials and binders are known to the person skilled in the art. For example, the cathode may comprise carbon in a conductive polymorph, for example selected from graphite, carbon black, carbon nanotubes, graphene or mixtures of at least two of the aforementioned substances. In addition, the cathode may comprise one or more binders, for example one or more organic polymers like polyethylene, polyacrylonitrile, polybutadiene, polypropylene, polystyrene, polyacrylates, polyvinyl alcohol, polyisoprene and copolymers of at least two comonomers selected from ethylene, propylene, styrene, (meth)acrylonitrile and 1,3-butadiene, especially styrene-butadiene copolymers, and halogenated (co)polymers like polyvinlyidene chloride, polyvinly chloride, polyvinyl fluoride, polyvinylidene fluoride (PVdF), polytetrafluoroethylene, copolymers of tetrafluoroethylene and hexafluoropropylene, copolymers of tetrafluoroethylene and vinylidene fluoride and polyacrylnitrile.
The anode comprised within the lithium batteries of the present invention comprises an anode active material that can reversibly occlude and release lithium ions or is capable to form an alloy with lithium. In particular carbonaceous material that can reversibly occlude and release lithium ions can be used as anode active material. Carbonaceous materials suited are crystalline carbon such as a graphite material, more particularly, natural graphite, graphitized cokes, graphitized MCMB, and graphitized MPCF; amorphous carbon such as coke, mesocarbon microbeads (MCMB) fired below 1500° C., and mesophase pitch-based carbon fiber (MPCF); hard carbon and carbonic anode active material (thermally decomposed carbon, coke, graphite) such as a carbon composite, combusted organic polymer, and carbon fiber.
Further anode active materials are lithium metal, or materials containing an element capable of forming an alloy with lithium. Non-limiting examples of materials containing an element capable of forming an alloy with lithium include a metal, a semimetal, or an alloy thereof. It should be understood that the term “alloy” as used herein refers to both alloys of two or more metals as well as alloys of one or more metals together with one or more semimetals. If an alloy has metallic properties as a whole, the alloy may contain a nonmetal element. In the texture of the alloy, a solid solution, a eutectic (eutectic mixture), an intermetallic compound or two or more thereof coexist. Examples of such metal or semimetal elements include, without being limited to, titanium (Ti), tin (Sn), lead (Pb), aluminum, indium (In), zinc (Zn), antimony (Sb), bismuth (Bi), gallium (Ga), germanium (Ge), arsenic (As), silver (Ag), hafnium (Hf), zirconium (Zr) yttrium (Y), and silicon (Si). Metal and semimetal elements of Group 4 or 14 in the long-form periodic table of the elements are preferable, and especially preferable are titanium, silicon and tin, in particular silicon. Examples of tin alloys include ones having, as a second constituent element other than tin, one or more elements selected from the group consisting of silicon, magnesium (Mg), nickel, copper, iron, cobalt, manganese, zinc, indium, silver, titanium (Ti), germanium, bismuth, antimony and chromium (Cr). Examples of silicon alloys include ones having, as a second constituent element other than silicon, one or more elements selected from the group consisting of tin, magnesium, nickel, copper, iron, cobalt, manganese, zinc, indium, silver, titanium, germanium, bismuth, antimony and chromium.
A further possible anode active material are silicon based materials. Silicon based materials include silicon itself, e.g. amorphous and crystalline silicon, silicon containing compounds like SiOx with 0<x<1.5 and Si alloys, and compositions containing silicon and/or silicon containing compounds, e.g. silicon/graphite composites. The silicon may be used in different forms, e.g. in the form of nanowires, nanotubes, nanoparticles, films, nanoporous silicon or silicon nanotubes. The silicon may be deposited on a current collector. The current collector may be a metal wire, a metal grid, a metal web, a metal sheet, a metal foil or a metal plate. Preferred the current collector is a metal foil, e.g. a copper foil. Thin films of silicon may be deposited on metal foils by any technique known to the person skilled in the art, e.g. by sputtering techniques. One possibility of preparing Si thin film electrodes are described in R. Elazari et al.; Electrochem. Comm. 2012, 14, 21-24.
Other possible anode active materials are lithium ion intercalating oxides of Ti.
Preferably the anode active material is selected from carbonaceous material that can reversibly occlude and release lithium ions, particularly preferred the carbonaceous material that can reversibly occlude and release lithium ions is selected from crystalline carbon, hard carbon and amorphous carbon, in particular preferred is graphite. In another preferred embodiment the anode active is selected from silicon that can reversibly occlude and release lithium ions, preferably the anode comprises a thin film of silicon or a silicon/carbon mixture. In a further preferred embodiment the anode active is selected from lithium ion intercalating oxides of Ti.
The anode and cathode may be made by preparing an electrode slurry composition by dispersing the electrode active material, a binder, optionally a conductive material and a thickener, if desired, in a solvent and coating the slurry composition onto a current collector. The current collector may be a metal wire, a metal grid, a metal web, a metal sheet, a metal foil or a metal plate. Preferred the current collector is a metal foil, e.g. a copper foil or aluminum foil.
The inventive lithium batteries may contain further constituents customary per se, for example separators, housings, cable connections etc. The housing may be of any shape, for example cuboidal or in the shape of a cylinder, the shape of a prism or the housing used is a metal-plastic composite film processed as a pouch. Suited separators are for example glass fiber separators and polymer-based separators like polyolefin separators.
Several inventive lithium batteries may be combined with one another, for example in series connection or in parallel connection. Series connection is preferred. The present invention further provides for the use of inventive lithium ion batteries as described above in devices, especially in mobile devices. Examples of mobile devices are vehicles, for example automobiles, bicycles, aircraft, or water vehicles such as boats or ships. Other examples of mobile devices are those which are portable, for example computers, especially laptops, telephones or electrical power tools, for example from the construction sector, especially drills, battery-driven screwdrivers or battery-driven tackers. But the inventive lithium ion batteries can also be used for stationary energy stores.
Even without further statements, it is assumed that a skilled person is able to utilize the above description in its widest extent. Consequently, the preferred embodiments and examples are to be interpreted merely as a descriptive enclosure which in no way has any limiting effect at all.
The invention is illustrated by the examples which follow, which do not, however, restrict the invention.
A mixture of 5,6-dichloro-2,3-dicyanopyrazine (10.54 g, 52.97 mmol) and methanol (MeOH) (270 ml) was warmed to 50° C. and triethylamine (10.93 g, 108 mmol) was added dropwise. The mixture was heated to reflux and stirred for 20 hours. After cooling to room temperature (RT) the mixture was concentrated on the rotary evaporator, then water (400 ml) and CH2Cl2 (400 ml) were added and the phases separated. The aqueous phase was extracted with CH2Cl2 and the combined organic phases washed with water, dried over Na2SO4 and the solvent evaporated. The crude product (9.05 g) was dissolved in warm tetrahydrofurane (THF) (200 ml) and ice-water (200 ml) was added. The precipitated solid was collected by filtration, washed with cyclohexane and dried to provide the desired product as green solid (5.94 g).
To a mixture of 5,6-dichloro-2,3-dicyanopyrazine (10.16 g, 51.06 mmol) in THF (270 ml) triethylamine (10.59 g, 104.65 mmol) was added at RT. Then benzylalcohol (13.8 g, 127.6 mmol) was added dropwise at RT. AFterwards the mixture was heated to reflux, stirred for 18 hours and cooled to RT. The solids were filtered off and to the filtrate ice-water (1000 ml) was added. The precipitated solid was collected by filtration, washed with cyclohexane and dried. The crude product (7.08 g) was recrystallized (acetone/n-hexane) to give the desired product as yellow-green solid (5.02 g).
To a mixture of diaminomaleonitrile (2.16 g, 20 mmol) and H2SO4 (1 ml) in MeOH (50 ml) was added a solution of 1,2-diphenylethane-1,2-dione (4.30 g, 20 mmol) in MeOH (150 ml) at 45° C. A precipitate started to form. The mixture was stirred 2 hours at 45° C. and 1.5 hours at reflux. After cooling to RT the precipitate was filtered, washed with cyclohexane and dried to give the desired product (5.27 g) as beige solid.
To a mixture of 5,6-dichloro-2,3-dicyanopyrazine (10.00 g, 50.25 mmol) in THF (270 ml) triethylamine (10.42 g, 102.97 mmol) was added at RT. Then thiophenol (12.18 g, 110.55 mmol) was added dropwise during which the temperature raised from RT to 41° C. and a white precipitate was formed. The mixture was stirred at reflux overnight then cooled to RT and the solids were filtered off. The filtrate was concentrated and CH2Cl2 (200 ml) and aq. NaHCO3 (200 ml) were added to the residue and the phases separated. The organic phase was washed with aq. NaHCO3 (200 ml) and water (2×200 ml), dried over Na2SO4 and the solvent evaporated. The crude product (14.3 g) was recrystallized from isopropanol to give the desired product as brown solid (9.37 g).
To a mixture of NaH (4.2 g, 60% in mineral oil, 0.11 mmol) in THF (50 ml) 2,2,2-trifluoroethanol (10.75 g, 0.11 mmol) in THF (50 ml) was added dropwise at 0° C. over 30 min.
After stirring for 2 hours, a solution of 5,6-dichloro-2,3-dicyanopyrazine (10.2 g, 50 mmol) in THF (50 ml) was added over 12 min at 0° C. The reaction mixture was stirred 1 hour at 0° C. then warmed to RT and stirred overnight. The mixture was quenched with aq. NH4Cl (100 ml) and extracted with CH2Cl2 (1×100 ml and 2×50 ml), the combined organic phases dried over Na2SO4 and the solvent evaporated. The crude product was recrystallized from isopropanol and dried to give the desired product (7.14 g) as yellow-green solid.
To a mixture of 5,6-dichloro-2,3-dicyanopyrazine (10.00 g, 50.25 mmol) in THF (270 ml) triethylamine (10.42 g, 102.97 mmol) was added at RT. Then benzyl mercaptan (13.73 g, 110.54 mmol) was added dropwise, during which the temperature raised from RT to 50° C. The mixture was stirred at RT for 5 hours then cooled to 0° C. and the solids were filtered off. The filtrate was concentrated and CH2Cl2 (200 ml) and aq. NaHCO3 (200 ml) were added to the residue and the phases separated. The organic phase was washed with aq. NaHCO3 (200 ml) and water (200 ml), dried over Na2SO4 and the solvent evaporated. The crude product (19 g) was recrystallized from isopropanol to give the desired product as violet solid (12.8 g).
Electrolyte compositions were prepared from ethylene carbonate (EC), diethyl carbonate (DEC), LiPF6, adiponitrile, 1,4,5,6-tetrahydro-5,6-dioxo-2,3-pyrazinedicarbonitrile and compounds 1.1 to 1.4. The compositions are indicated in Table 1, “wt.-%” are based on the total weight of the electrolyte composition.
Commercially available wound pouch dry cells (Lithium Cobalt Oxide vs Graphite) were dried at 70° C. in vacuo for 24 h then filled with 700 μl electrolyte under Argon atmosphere. After 5 h rest at room temperature the cells were evacuated and sealed. The cells were then cycled between 2.75 and 4.4V for 5 cycles, charged to 4.4V and stored at 85° C. for 24 h.
The volume change of the cells was measured before and after 85° C. storage by using Archimedes' principle. This method is known to those skilled in the art. The results of the experiments are shown in Table 1.
The amount of Co dissolved from the cathode in electrolyte and migrated to the graphite electrode was determined by ICP-OES (inductively coupled plasma optical emission spectrometry) after storage at 85° C. for 24 h. The lower the value the better. All values are normalized to comparative example 2 with comparative example 2 being assigned a value of 100. The results of the experiments are shown in Table 1.
All inventive electrolyte compositions containing a cyclic dinitrile of formula (I) show at least lower Co dissolution or lower change of volume after 24 h storage at 85° C. than electrolyte compositions containing a dinitrile already known as electrolyte additive.
| Number | Date | Country | Kind |
|---|---|---|---|
| 15181137.9 | Aug 2015 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2016/069078 | 8/10/2016 | WO | 00 |
