Patent Application
20170214097
The present invention is directed towards liquid formulations comprising
wherein:
Furthermore, the present invention is directed towards a process for making formulations according to the present invention. Furthermore, the present invention is directed towards a use, and a method of use, of the formulation according to the present invention.
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 rechargeability. Secondary lithium batteries are of special interest for energy storage since they provide high energy density due to the small atomic weight and the large ionization energy of lithium and have become widely used as a power source for many portable electronics such as cellular phones, laptop computers, mini-cameras, etc.
If lithium ion batteries are charged in excess of their nominal voltage, e.g. by a defect in the charging station, the batteries tend to heat up which can in the worst case lead to a thermal runaway. As lithium ion batteries typically comprise flammable components such as the electrolyte compositions or the anode, the heat generated when overcharged can lead to ignition.
One possibility to deal with the safety hazard is the addition of overcharge protection additives. Known overcharge protection additives may terminate cell operation permanently. Such additives are, for example, aromatic compounds like biphenyl and cyclohexylphenyl, which polymerize at the cathode to release gas. The resulting polymer isolates the cathode from further overcharging while the gas activates a current interrupting device. EP 1 335 445 discloses a combination of aromatic compounds as electrolyte additives that polymerize upon oxidative initiation in the electrolyte when the battery is overcharged. However, the development of novel cathode active materials allowing the use of a lithium ion battery at higher voltages requires overcharge protection additives being effective at higher voltages, too.
EP 2 490 291 A1 discloses combinations of 1,2,3,4-tetrahydronaphthalene and certain biphenyl derivatives as overcharge protection additive in lithium ion batteries. However, the energy density of such electrochemical cells leaves room for improvement.
U.S. Pat. No. 7,968,839 suggests to add 0.001 to 0.8% by weight of certain preferably mono-substituted biphenyl derivatives in order to improve the battery performance.
It is the objective of the present invention to provide alternative overcharge protection additives and to preferably increase the safety of an electrochemical cell, in particular its overcharge protection efficiency at higher voltages. At the same time electrochemical cells comprising said overcharge protection additives should show high electrochemical performance over a wide temperature range, in particular cycle stability, energy density, power capability and a long shelf life.
Accordingly, the liquid formulations defined at the outset have been found, hereinafter also being referred to as formulations according to the invention, formulations according to the present invention or more briefly, inventive formulations.
Inventive formulations are liquid. That shall mean in the context of the present invention that they are liquid at ambient temperature. Preferably, inventive formulations are liquid at temperatures lower than ambient temperature, for example at −30° C. or even −40° C. Such liquid formulations are particularly suitable for outdoor applications, for example for use in automotive batteries.
Inventive formulations contain
According to one embodiment the electrolyte composition may contain up to ten different solvents (A).
Solvent (A) 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 acetals and ketals, orthocarboxylic acids esters, cyclic and acyclic esters of carboxylic acids, cyclic and acyclic sulfones, and cyclic and acyclic nitriles and dinitriles.
More preferably, solvent (A) is selected from cyclic and acyclic organic carbonates, di-C1-C10-alkylethers, di-C1-C4-alkyl-C2-C6-alkylene ethers and polyethers, cyclic and acyclic acetals and ketals, and cyclic and acyclic esters of carboxylic acids, even more preferred the solvent (A) is selected from cyclic and acyclic organic carbonates, and most preferred, inventive formulations contain at least two solvents (A) selected from cyclic and acyclic organic carbonates, in particular preferred inventive formulations contain at least one solvent (A) selected from cyclic organic carbonates and at least one solvent (A) selected from acyclic organic carbonates.
Solvent (A) may be partly halogenated, e.g. they may be partly fluorinated, partly chlorinated or partly brominated, and preferably solvent (A) may be partly fluorinated. “Partly halogenated” means, that one or more H of the respective molecule is replaced 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 solvents (A), i.e. the electrolyte composition may contain a mixture of partly halogenated and non-halogenated solvents (A).
Examples of cyclic organic 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 organic carbonates are ethylene carbonate, monofluoroethylene carbonate and propylene carbonate, in particular ethylene carbonate.
Examples of acyclic organic carbonates are di-C1-C10-alkylcarbonates wherein each alkyl group may be 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), methylpropyl carbonate, di-n-propyl carbonate and diisopropylcarbonate. Preferred acyclic organic carbonates are diethyl carbonate (DEC), ethyl methyl carbonate (EMC), and dimethyl carbonate (DMC).
In one embodiment of the invention the electrolyte composition contains mixtures of acyclic organic carbonates and cyclic organic carbonates at a ratio by weight of from 1:10 to 10:1, preferred of from 3:1 to 1:1.
According to the invention each alkyl group of di-C1-C10-alkylethers may be selected independently from the other. Examples of di-C1-C10-alkylethers are dimethylether, ethylmethylether, 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.
In addition, inventive formulations comprise
Lithium salt (B) is preferably selected from the group consisting of
Suited 1,2- and 1,3-diols from which the group (O-A1-O) 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 respective alkyl group are replaced by F.
Suitable 1,2- or 1,3-dicarboxlic acids from which the bivalent group (O-A1-O) may be 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.
Suitable 1,2- or 1,3-hydroxycarboxylic acids from which the bivalent group (O-A1-O) may be 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(R3)4], Li[B(R3)2(O-A1-O)] and Li[B(O-A1-O)2] are LiBF4, lithium difluoro oxalato borate and lithium dioxalato borate.
Preferably lithium salt (B) is selected from LiPF6, LiBF4, and LiPF3(CF2CF3)3, and more preferably, lithium salt (B) is selected from LiPF6 and LiBF4, and the most preferred lithium salt (B) is LiPF6.
In one embodiment of the present invention, lithium salt (B) is present at a minimum concentration of at least 0.1 m/l, preferably the concentration of the at least one conducting salt is 0.5 to 2 mol/l based on the entire inventive formulation.
Furthermore, formulations according to the present invention contain at least 1.5% by weight of one compound according to formula (I)
wherein:
In one embodiment of the present invention R1 is CH3. In one embodiment of the present invention a is zero.
In one embodiment of the present invention compound (I) is compound (1 a).
Furthermore, inventive formulations essentially contain no 1,2,3,4-tetrahydronaphthalene. In the context of the present invention, “essentially contain no 1,2,3,4-tetrahydronaphthalene” means that the respective formulations contain zero to 0.01% by weight of 1,2,3,4-tetrahydronaphthalene, said percentage referring to the whole respective liquid formulation.
Inventive formulations can be used as electrolytes for lithium ion batteries and for their respective electrochemical cells, for all or for some.
In one embodiment of the present invention formulations according to the present invention may comprise
One class of additives (E) are polymers, hereinafter also being referred to as polymers (E). Polymers may be selected from polyvinylidene fluoride, polyvinylidene-hexafluoropropylene copolymers, polyvinylidene-hexafluoropropylene-chlorotrifluoroethylene copolymers, Nafion, polyethylene oxide, polymethyl methacrylate, polyacrylonitrile, polypropylene, polystyrene, polybutadiene, polyethylene glycol, polyvinylpyrrolidone, polyaniline, polypyrrole and/or polythiophene. Polymers (E) may be added to a formulation according to the present invention in order to convert liquid formulations into quasi-solid or solid electrolytes and thus to improve solvent retention, especially during ageing.
One other class of additives (E) are carbonates with a C—C double bond, for example vinylene carbonate, methylene ethylene carbonate and vinyliden ethylene carbonate.
One other class of additives (E) are flame retardants, hereinafter also being referred to as flame retardants (E). Examples of flame retardants (E) 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.
One other class of additives (E) are HF— and/or H2O scavengers. Examples of HF and/or H2O scavenger are optionally halogenated cyclic and acyclic silylamines.
Another class of additives (A) are so-called SEI-forming additives. An SEI forming additive according to the present invention is a compound which decomposes on an electrode to form a passivation layer on the electrode which prevents degradation of the electrolyte and/or the electrode. In this way, the lifetime of a battery is significantly extended. Preferably the SEI forming additive forms a passivation layer on the anode. An anode in the context of the present invention is understood as the negative electrode of a battery. Preferably, the anode has a reduction potential of 1 Volt or less against lithium such as a lithium intercalating graphite anode. In order to determine if a compound qualifies as anode film forming additive, an electrochemical cell can be prepared comprising a graphite electrode and a metal counter electrode, and an electrolyte containing a small amount of said compound, typically from 0.1 to 10 wt.-% of the electrolyte composition, preferably from 0.2 to 5 wt.-% of the electrolyte composition. Upon application of a voltage between anode and lithium metal, the differential capacity of the electrochemical cell is recorded between 0.5 V and 2 V. If a significant differential capacity is observed during the first cycle, for example −150 mAh/V at 1 V, but not or essentially not during any of the following cycles in said voltage range, the compound can be regarded as SEI forming additive.
According to the present invention the electrolyte composition preferably contains at least one SEI forming additive. SEI forming additives are known to the person skilled in the art. More preferred the electrolyte composition contains at least one SEI forming selected from 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; oprganic sultones such as propylene sultone, propane sultone and their 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; and ionic compounds containing a cation of formula (II)
wherein
Z is CH2 or NR13,
R5 is selected from C1 to C6 alkyl,
R6 is selected from —(CH2)u—SO3—(CH2)v—R14,
—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)u— 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 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,
R13 is selected from C1 to C6 alkyl,
R14 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 R14 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 R14 include methyl, ethyl, trifluoromethyl, pentafluoroethyl, n-propyl, n-butyl, n-hexyl, ethenyl, ethynyl, allyl or prop-1-yn-yl,
and an anion selected from bisoxalato borate, difluoro (oxalato) borate, [FzB(CnF2y+1)4-z]−, [FyP(CnF2n+1)6-y]−, (CyF2n+1)2P(O)O]−, [CyF2n+1P(O)O2]2−, [O—C(O)—CnF2n+1]−, [O—S(O)2—CnF2n+1]−, [N(C(O)—CnF2n+1)2]−, [N(S(O)2—CnF2n+1)2]−, [N(C(O)—CnF2n+1)(S(O)2—CnF2n+1)]−, [N(C(O)CnF2n+1)(C(O)F)]−, [N(S(O)2—CnF2n+1)(S(O)2F)]−, [N(S(O)2F)2]−, [C(C(O)—CnF2n+1)3]−, [C(S(O)2—CnF2n+1)3]−, wherein n is an integer from 1 to 20, preferably up to 8, z is an integer from 1 to 4, and y is an integer from 1 to 6,
Preferred anions 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]−, [O—S(O)2CF3]−, [O—S(O)2C2F5]−, [N(C(O)C2F5)2]−, [N(C(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]−.
The term “C2-C20 alkenyl” as used herein refers to an unsaturated straight or branched hydrocarbon group with 2 to 20 carbon atoms having one free valence. Unsaturated means that the alkenyl group contains at least one C—C double bond. C2-C6 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 and the like. Preferred are C2-C10 alkenyl groups, more preferred are C2-C6 alkenyl groups, even more preferred are C2-C4 alkenyl groups and in particular ethenyl and 1-propen-3-yl (allyl).
The term “C2-C20 alkynyl” as used herein refers to an unsaturated straight or branched hydrocarbon group with 2 to 20 carbon atoms having one free valence, wherein the hydrocarbon group contains at least one C—C triple bond. C2-C6 alkynyl includes for example ethynyl, 1-propynyl, 2-propynyl, 1-n-butinyl, 2-n-butynyl, iso-butinyl, 1-pentynyl, 1-hexynyl, 1-heptynyl, 1-octynyl, 1-nonynyl, 1-decynyl and the like and the like. Preferred are C2-C10 alkynyl, more preferred are C2-C6 alkynyl, even more preferred are C2-C4 alkynyl, in particular preferred are ethynyl and 1-propyn-3-yl (propargyl).
The term “C6-C12 aryl” as used herein denotes an aromatic 6- to 12-membered hydrocarbon cycle or condensed cycles having one free valence. Examples of C6-C12 aryl are phenyl and naphtyl. Preferred is phenyl.
The term “C7-C24 aralkyl” as used herein denotes an aromatic 6- to 12-membered aromatic hydrocarbon cycle or condensed aromatic cycles substituted by one or more C1-C6 alkyl. The C7-C24 aralkyl group contains in total 7 to 24 C-atoms and has one free valence. The free valence may be located at the aromatic cycle or at a C1-C6 alkyl group, i.e. C7-C24 aralkyl group may be bound via the aromatic part or via the alkyl part of the aralkyl group. Examples of C7-C24 aralkyl are methylphenyl, benzyl, 1,2-dimethylphenyl, 1,3-dimethylphenyl, 1,4-dimethylphenyl, ethylphenyl, 2-propylphenyl, and the like.
Compounds of formula (II) and their preparation are described in detail in WO 2013/026854 A1. Examples of compounds of formula (II) which are preferred according to the present invention are disclosed on page 12, line 21 to page 15, line 13 of 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), 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 (E) 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 may also be added as conducting salt.
In one embodiment of the present invention formulations additive (E) is selected from organic phosphates, organic phosphonates, organic sultones, and LiBOB.
In one embodiment of the present invention, inventive formulations contain:
in total 0.1 to 25% by weight of lithium salt (B), preferably 10 to 20% by weight,
in total 1.5 to 10% of compound according to formula (I), preferably 2 to 5% by weight, even more preferably 3 to 5% by weight,
zero to 0.01% by weight of 1,2,3,4-tetrahydronaphthalene (D), and
zero to in total 30% of additive(s) (E), preferably 1 to 10% by weight,
percentages referring to the whole respective liquid formulation.
In one embodiment of the present invention, the water content of inventive formulations is preferably below 100 ppm, based on the weight of the respective inventive formulation, 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 minimum water content of inventive formulations may be selected from 3 ppm, preferably 5 ppm.
In one embodiment of the present invention, the HF-content of inventive formulations is preferably below 100 ppm, based on the weight of the respective inventive formulation, more preferred below 50 ppm, most preferred below 30 ppm. The minimum HF content of inventive formulations may be selected from 5 ppm, preferably 10 ppm. The HF content may be determined by titration.
Compounds of the formula (I), as described above or as described as being preferred, may be used as overcharge protection additive in an electrolyte composition for electrochemical cells. Therefore, a further aspect of the present invention is the use of compounds of formula (I) as described above as overcharge protection additives in electrolyte compositions.
Another aspect of the present invention is the use of inventive formulations in or for the manufacture of electrochemical cells. Such electrochemical cells may be used as or for the manufacture of lithium ion batteries. Another aspect of the present invention is a method of use of inventive formulations.
In particular preferred embodiments such electrochemical cell is part of a lithium ion battery, i.e. a secondary lithium ion electrochemical cell comprising a cathode (a) comprising a cathode active material that can reversibly occlude and release lithium ions and an anode (b) 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.
Another aspect of the present invention is thus an electrochemical cell comprising
Preferably, cathode active materials are selected from a material capable of occluding and releasing lithium ions selected from lithiated transition metal phosphates and from lithium ion intercalating metal oxides.
Examples of lithiated transition metal phosphates are LiMnPO4, LiFePO4 and LiCoPO4, examples of lithium ion intercalating metal oxides are LiCoO2, LiNiO2, mixed transition metal oxides with a layered structure, generally 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 LiMn2O4 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 lithium nickel cobalt aluminum oxides, the latter being materials of general formula Li(1+g)[NihCOiAlj](1−g)O2+k. Typical values for g, h, i, j and k are: g=0 to 0.1, h=0.8 to 0.85, i=0.15 to 0.20, j=0.02 to 0.03 and k=0.
In a preferred embodiment of the present invention cathode (a) contains at least one cathode active material selected from LiCoO2, lithium nickel cobalt aluminum oxide, and layered lithiated nickel-cobalt-manganese oxide.
Cathode (a) may further comprise electrically conductive materials like electrically conductive carbon. Cathode (a) may further comprise components like binders. For example, cathode (a) 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.
Cathode (a) 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 styrenebutadiene 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.
Anode (b) 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 examples of anode active materials are lithium metal and 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 is silicon that is able to intercalate lithium ions. 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 (c). Current collector (c) may be selected from coated metal wires, a coated metal grid, a coated metal web, a coated metal sheet, a coated metal foil or a coated metal plate. Preferably, current collector (c) is a coated metal foil, e.g. a coated 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 method of preparing thin silicon film electrodes are described in R. Elazari et al.; Electrochem. Comm. 2012, 14, 21-24. It is also possible to use a silicon/carbon composite as anode active material.
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, particularly preferred is graphite. In another preferred embodiment the anode active material is selected from silicon. Silicon can reversibly occlude and release lithium ions. Preferably, anode (b) comprises a thin film of silicon or a silicon/carbon composite. In a further preferred embodiment the anode active material is selected from lithium ion intercalating oxides of Ti.
Anode (b) and cathode (a) 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 electrochemical cells 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 staplers. But the inventive lithium ion batteries can also be used for stationary energy stores.
The present invention is further illustrated by the following examples that do not, however, restrict the invention.
Compound of formula (I a) was synthesized by reacting 2-phenylpenol with CH3SO2—Cl in the presence of triethylamine as a base.
The following components were used:
In a glove box under argon, 1 M solution of (B.1) in (A.1)/(A.2) 3:7 by weight was prepared. To this solution (I a), (D) and (E)—if applicable—were added in accordance with Table 1.
The components of inventive formulations and comparative formulations are summarized in Table 1. Percentages are percentages in weight and refer to the total respective formulation.
Button cells were fabricated using lithium nickel cobalt manganese oxide (LiNi0.33Co0.33Mn0.33O2; NCM 111) electrodes with a capacity of 2 mAh/cm2 and a graphite electrode with a capacity of 2.15 mAh/cm2. A glass-fiber filter separator (Whatmann GF/D) was used as separator, which was soaked with 100 μl of the respective electrolyte composition. All electrochemical measurements were carried out at 25° C. in climate chambers. For electrochemical testing the procedure displayed in Table 2 was used.
General remark: After reaction of the overcharge protection additive the cycling capacity is zero in the cycling test and the cell is irreversibly deactivated. If no overcharge protection additive is used or if it is not effective the cell still shows a high capacity.
If the overcharge additive starts to react a plateau can be seen in the voltage vs. time plot of the cycling experiment. The plateau is caused by the oxidative faradic reactions which take place due to the decomposition of the overcharge additive. The voltage value at which the reaction starts is called onset voltage. A higher onset voltage of the overcharge additive enables higher cut off voltages for the battery and consequently higher energy density can be realized.
The cycling performance is summarized in Table 3, the passivation in Table 4.
The cycling performance was as follows.
| Number | Date | Country | Kind |
|---|---|---|---|
| 14177675.7 | Jul 2014 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2015/066434 | 7/17/2015 | WO | 00 |
