Patent Application
20200287242
The present invention relates to a lithium ion battery comprising
The present invention further relates to the use of at least one compound selected from the group consisting of lithium (bisoxalato) borate, lithium difluoro (oxalato) borate, lithium tetrafluoro (oxalato) phosphate, lithium oxalate, lithium (malonato oxalato) borate, lithium (salicylato oxalato) borate, lithium (tris oxalato) phosphate and compounds of formula (I) as defined above in combination with at least one compound of general formula (IIa) or (IIb) as defined above, as additives in electrolytes of lithium ion batteries comprising a cathode active material selected from lithium ion containing transition metal compounds having a content of Manganese of from 50 to 100 wt.-% based on the total weight of the transition metal in the lithium ion containing transition metal compound, wherein compound (B) is used in a concentration range of from 0.01 up to less than 5 wt.-% and the compound (C) is used in a concentration range of from 0.01 up to less than 5 wt.-% based on the total weight of the electrolyte composition.
The term “compound (B)” denotes the compounds listed under (B) in the electrolyte composition, i.e. compound (B) denotes the group consisting of lithium (bisoxalato) borate, lithium difluoro (oxalato) borate, lithium tetrafluoro (oxalato) phosphate, lithium oxalate, lithium (malonato oxalato) borate, lithium (salicylato oxalato) borate, lithium (tris oxalato) phosphate and compounds of formula (I) as defined above.
The term “compound (C)” denotes the compounds listed under (C) in the electrolyte composition, i.e. compound (C) denotes the group of compounds of general formula (IIa) or (IIb) as defined above.
Storing energy has long been a subject of growing interest. Electrochemical cells, for example batteries or accumulators, can serve to store electrical energy. As of recently, what are called lithium ion batteries have attracted particular interest. They are superior to the conventional batteries in several technical aspects. Lithium ion batteries are water sensitive. Water is therefore out of the question as a solvent for the lithium salts used in lithium ion batteries. Instead, organic carbonates, ethers and esters are used as sufficiently polar solvents. The literature accordingly recommends using water-free solvents for the electrolytes; see for example WO 2007/049888.
An important role is played by the materials from which the electrodes are made, and especially the material from which the cathode is made. Furthermore, the decomposition of the electrolyte or electrolyte components on the surface of the electrode materials (anode and cathode) is critical for the battery performance and battery cycle lifetime.
In many cases, lithium-containing mixed transition metal oxides are used as cathode active materials in lithium ion batteries, especially lithium-containing nickel-cobalt-manganese oxides with layer structure, or manganese-containing spinels which may be doped with one or more transition metals. These manganese-containing cathode active materials are promising due to their high operation voltage. However, a problem with many batteries remains that of cycling stability, which is still in need of improvement. Specifically in the case of those batteries which comprise a comparatively high proportion of manganese, for example in the case of electrochemical cells with a manganese-containing spinel electrode and a graphite anode, a severe loss of capacity is frequently observed within a relatively short time. In addition, it is possible to detect deposition of elemental manganese on the anode in cases where graphite anodes are selected as counter electrodes. It is believed that these manganese nuclei deposited on the anode, at a potential of less than 1V vs. Li/Li+, act as a catalyst for a reductive decomposition of the electrolyte. This is also thought to involve irreversible binding of lithium, as a result of which the lithium ion battery gradually loses capacity. Other transition metals contained in the cathode active material may be dissolved in the electrolyte during cycling the electrochemical cell analogously. These transition metals migrate towards the anode and are reduced and deposited on the anode due to the low potential. Even small amounts of such metal impurities may change the interface between electrolyte and anode and may lead to a reduced life time of the battery.
WO 2011/024149 discloses lithium ion batteries which comprise an alkali metal such as lithium between cathode and anode, which acts as a scavenger of unwanted by-products or impurities. Both in the course of production of secondary battery cells and in the course of later recycling of the spent cells, suitable safety precautions have to be taken due to the presence of highly reactive alkali metal.
Dalavi, S. et al., Journal of The Electrochemical Society 157 (2010), pages A1113 to A1120 describes the use of dimethyl methyl phosphonate as flame retardant for lithium ion batteries comprising as cathode active material LiNi0.8Co0.2O2. This metal oxide has a comparatively low cell voltage in range of from 3.0 to 4.1 V.
It was thus an object of the present invention to provide means for reducing the dissolution of transition metal components like nickel and especially manganese from the cathode active material of lithium ion batteries and reducing the migration of transition metals from the cathode to the anode. It was further an object of the present invention to provide an electrolyte composition leading to an improved lifetime of lithium ion batteries comprising Manganese in the cathode active material, especially for high voltage Li ion batteries comprising Manganese in the cathode active material. Finally it was an object of the present invention to provide lithium ion batteries comprising Manganese in the cathode active material and having good performance characteristics.
This object is achieved by a lithium ion battery comprising
The addition of at least one compound of general formula (IIa) or (IIb) in combination with at least one compound selected from the group consisting of compounds of formula (I), lithium (bisoxalato) borate, lithium difluoro (oxalato) borate, lithium tetrafluoro (oxalato) phosphate, lithium oxalate lithium (malonato oxalato) borate, lithium (salicylato oxalato) borate, and lithium (tris oxalato) phosphate as additives in an electrolyte in the concentration ranges mentioned above reduces the dissolution of transition metal from cathode active materials containing transition metal compounds. Lithium ion batteries comprising the inventive electrolyte compositions have increased cycling stability.
The electrolyte composition (iii) of the inventive lithium ion battery 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 electrolyte composition (iii) contains at least one aprotic organic solvent (A), preferably at least two aprotic organic solvents (A) and more preferred at least three aprotic organic solvents (A). According to one embodiment the electrolyte composition may contain up to ten aprotic organic solvents (A).
The at least one aprotic organic solvent (A) is preferably selected from
More preferred the at least one aprotic organic solvent (A) is selected from cyclic and noncyclic organic carbonates (a), di-C1-C10-alkylethers (b), di-C1-C4-alkyl-C2-C6-alkylene ethers and polyethers (c) and cyclic und acyclic acetales and ketales (e), even more preferred the composition contains at least one aprotic organic solvent (A) selected from cyclic and noncyclic organic carbonates (a) and most preferred the composition contains at least two aprotic organic solvents (A) selected from cyclic and noncyclic organic carbonates (a).
Among the aforesaid aprotic organic solvents (A) such solvents and mixtures of solvents (A) are preferred which are liquid at 1 bar and 25° C.
Examples of suitable organic carbonates (a) are cyclic organic carbonates according to the general formula (IIIa), (IIIb) or (IIIc)
wherein
R8, R9 und R10 being different or equal and being independently from each other selected from hydrogen and C1-C4-alkyl, preferably methyl; F, and C1-C4-alkyl substituted by one or more F, e.g. CF3.
“C1-C4-alkyl” is intended to include methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec.-butyl and tert.-butyl.
Preferred cyclic organic carbonates (a) are of general formula (IIIa), (IIIb) or (IIIc) wherein R8 and R9 are H. A further preferred cyclic organic carbonate (a) is difluoroethylencarbonate (IIId)
Examples of suitable non-cyclic organic carbonates (a) are dimethyl carbonate, diethyl carbonate, methylethyl carbonate and mixtures thereof.
In one embodiment of the invention the electrolyte composition contains mixtures of non-cyclic organic carbonates (a) and cyclic organic carbonates (a) at a ratio by weight of from 1:10 to 10:1, preferred of from 3:1 to 1:1.
Examples of suitable non-cyclic di-C1-C10-alkylethers (b) are dimethylether, ethylmethylether, diethylether, diisopropylether, and di-n-butylether.
Examples of di-C1-C4-alkyl-C2-C6-alkylene ethers (c) are 1,2-dimethoxyethane, 1,2-diethoxyethane, diglyme (diethylene glycol dimethyl ether), triglyme (triethylenglycol dimethyl ether), tetraglyme (tetraethylenglycol dimethyl ether), and diethylenglycoldiethylether.
Examples of suitable polyethers (c) 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 suitable cyclic ethers (d) are tetrahydrofurane and 1,4-dioxane.
Examples of suitable non-cyclic acetals (e) are 1,1-dimethoxymethane and 1,1-diethoxymethane. Examples for suitable cyclic acetals (e) are 1,3-dioxane and 1,3-dioxolane.
Examples of suitable orthocarboxylic acids esters (f) are tri-C1-C4 alkoxy methane, in particular trimethoxymethane and triethoxymethane.
Examples for suitable noncyclic esters of carboxylic acids (g) are ethyl acetate, methyl butanoate, esters of dicarboxylic acids like 1,3-dimethyl propanedioate. An example of a suitable cyclic ester of carboxylic acids (lactones) is γ-butyrolactone.
The electrolyte composition (iii) of the inventive Li ion battery further contains 0.01 up to less than 5 wt.-%, preferably 0.08 to 4 wt.-% and most preferred 0.015 to 3 wt.-%, based on the total weight of the electrolyte composition (iii), of at least one compound (B) selected from the group consisting of lithium (bisoxalato) borate (LiBOB), lithium difluoro (oxalato) borate (LiDFOB), lithium tetrafluoro (oxalato) phosphate, lithium oxalate and compounds of formula (I)
wherein R1 is selected from H and C1-C4 alkyl.
Compounds of formula (I) include vinylenecarbonate, methylvinylenecarbonate, ethylvinylenecarbonate, n-propylvinylenecarbonate, i-propylvinylenecarbonate, n-butylvinylenecarbonate, and i-butylvinylenecarbonate.
Preferably the electrolyte composition (iii) contains at least one compound (B) selected from the group consisting of lithium (bisoxalato) borate, lithium tetrafluoro (oxalato) phosphate, lithium oxalate, and lithium difluoro (oxalato) borate. According to one embodiment, the inventive composition contains vinylenecarbonate. According to another embodiment the inventive composition contains lithium (bisoxalato) borate. According to a further embodiment the electrolyte composition contains lithium difluoro (oxalato) borate. According to another embodiment the electrolyte composition contains lithium tetrafluoro (oxalato) phosphate. According to a further embodiment the electrolyte composition contains lithium oxalate.
Furthermore, the electrolyte composition (iii) of the inventive Li ion battery contains 0.01 up to less than 5 wt.-%, preferably 0.08 to 4 wt.-% and most preferred 0.015 to 3 wt.-%, based on the total weight of the electrolyte composition (iii), of at least one compound (C) of general formula (IIa) or (IIb)
Examples of C1-C10-alkyl include methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec.-butyl, tert.-butyl, n-pentyl, iso-pentyl, n-hexyl, iso-hexyl, sec.-hexyl, 2-ethylhexyl, n-octyl, n-nonyl and n-decyl, preferred are methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec.-butyl, tert.-butyl, in particular preferred are methyl and ethyl.
Examples of C3-C10 cycloalkyl are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl and cyclodecyl, preferred are cyclopentyl, cyclohexyl, cycloheptyl.
Examples of C6-C14 aryl are phenyl, 1-naphtyl, 2-naphtyl, 1-anthryl, 2-anthryl, 2-anthryl, 1-phenanthryl, 2-phenanthryl, 3-phenanthryl, 4-phenanthryl and 9-phenanthryl, preferred are phenyl, 1-naphtyl and 2-naphtyl, in particular preferred is phenyl.
“Benzyl” means the substituent —CH2—C6H6.
Examples of “C1-C4 alkyl substituted by one or more F” are —CH2F, —CHF2, —CF3 and —C3H6CF3.
Preferred compounds (C) are compounds of general formula (IIa) and (IIb) wherein R2 is selected from H, C1-C6 alkyl, benzyl and phenyl wherein alkyl, benzyl and phenyl may be substituted by one or more F, C1-C4 alkyl, benzyl, phenyl, or C1-C4 alkyl substituted by one or more F, and R3, R4, R5, R6 and R7 may be same or different and are independently from each other selected from C1-C6 alkyl, benzyl and phenyl wherein alkyl, benzyl and phenyl may be substituted by one or more F, C1-C4 alkyl, benzyl, phenyl, or C1-C4 alkyl substituted by one or more F.
More preferred are compounds of formula (IIa) wherein R2 is selected from H and C1-C6 alkyl, and R3 and R4 may be same or different and are independently from each other selected from C1-C6 alkyl, even more preferred R2 is selected from H and C1-C4 alkyl and R2 and R3 are independently from each other selected from C1-C4 alkyl.
In particular preferred are dimethyl methyl phosphonate, diethyl ethyl phosphonate, dimethyl ethyl phosphonate (R2 is ethyl and R3 and R4 are methyl), and diethyl methyl phosphonate (R2 is methyl and R3 and R4 are ethyl).
The addition of a combination of at least one compound (B) and at least one compound (C) to an electrolyte in lithium ion batteries comprising a Manganese containing transition metal compound as cathode active material has shown to reduce the amount of Manganese and further transition metal present in the cathode active material dissolved from cathodes containing transition metals and to enhance the performance of the electrolyte. Hence, another object of the present invention is the use of at least one compound (B) as defined above in combination with at least one compound (C) as defined above as additives in electrolytes for lithium ion batteries comprising at least one cathode containing a cathode active material selected from lithium ion containing transition metal compounds having a content of Manganese of from 50 to 100 wt.-% based on the total weight of transition metal in the lithium ion containing transition metal compound, preferably having a content of Manganese of from 50 to 80 wt.-%, based on the total weight of the transition metal.
Preferred combinations of compounds (B) and (C) for use as additives in electrolytes for the inventive lithium ion batteries and comprised in the electrolyte compositions (iii) are the combinations of lithium (bisoxalato) borate, vinylenecarbonate and/or lithium difluoro (oxalato) borate with compounds of formula (IIa) wherein R2 is selected from H and C1-C6 alkyl, and R3 and R4 may be same or different and are independently from each other selected from C1-C6 alkyl, even more preferred with compounds of formula (IIa) wherein R2 is selected from H and C1-C4 alkyl and R3 and R4 are independently from each other selected from C1-C4 alkyl. Most preferred are the combinations of lithium (bisoxalato) borate, vinylenecarbonate, and/or lithium difluoro (oxalato) borate with one or more compounds selected from the group consisting of dimethyl methyl phosphonate, diethyl ethyl phosphonate, dimethyl ethyl phosphonate, and diethyl methyl phosphonate, and in particular the combination of lithium (bisoxalato) borate and dimethyl methyl phosphonate, the combination of vinylenecarbonate and dimethyl methylphosphonate, and the combination of lithium difluoro (oxalato) borate and dimethyl methyl phosphonate. Inventive lithium ion batteries comprising electrolyte compositions (iii) containing the aforementioned combinations of compounds (B) and (C) are preferred, too.
The electrolyte composition (iii) further contains at least one lithium salt (D) different from compounds (B). Preferably the lithium salt (D) is a monovalent salt, i.e. a salt with monovalent anions. The lithium salt (D) may be selected from the group consisting of LiPF6, LiPF3(CF2CF3)3, LiCIO4, LiAsF6, LiBF4, LiCF3SO3, LiN(SO2F)2, Li2SiF6, LiSbF6, LiAlCl4, and salts of the general formula (CnF2n+1SO2)mXLi, where m and n are defined as follows:
m=1 when X is selected from oxygen and sulfur,
m=2 when X is selected from nitrogen and phosphorus,
m=3 when X is selected from carbon and silicon, and
n is an integer in the range from 1 to 20,
like LiC(CnF2n+1SO2)3 wherein n is an integer in the range from 1 to 20, and lithium imides such as LiN(CnF2n+1SO2)2, where n is an integer in the range from 1 to 20.
Preferably the lithium salt (D) is selected from LiPF6, LiBF4, and LiPF3(CF2CF3)3, and more preferred the lithium salt (D) is selected from LiPF6 and LiBF4, the most preferred lithium salt (D) is LiPF6.
The at least one lithium salt (D) different from compounds (B) is usually present at a minimum concentration of at least 0.01 wt.-%, preferably of at least 1 wt.-%, and more preferred of at least 5 wt.-%, based on the total weight of the electrolyte composition.
Moreover, the inventive electrolyte composition may contain at least one further additive (E). The further additive (E) is selected from additives for electrolytes different from compounds (A), (B), (C) and (D). Examples for the further additive (E) are 2- and 4-vinylpyrridine, cyclic exo-methylene carbonates, sultones, organic esters of inorganic acids, cyclic and acyclic alkanes having at a pressure of 1 bar a boiling point of at least 36° C. and aromatic compounds.
Examples of suitable aromatic compounds are biphenyl, cyclohexylbenzene and 1,4-dimethoxy benzene.
Sultones may be substituted or unsubstituted. Examples for suitable sultones are butane sulton and propylene sultone (IV) as shown below:
Examples for suitable cyclic exo-methylene carbonates are compound of formula (V)
wherein R11 and R12 may be same or different and are independently from each other selected from C1-C10 alkyl, and hydrogen. Preferably both R8 and R9 are methyl. Also preferred both R8 and R9 are hydrogen. A preferred cyclic exo-methylene carbonate is methylenethylene carbonate.
Furthermore, additive (E) may be selected from acyclic or cyclic alkanes, preferably alkanes having at a pressure of 1 bar a boiling point of at least 36° C. Examples of such alkanes are cyclohexane, cycloheptane und cyclododecane.
Further compounds suitable as additives (E) are organic ester of inorganic acids like ethyl ester or methyl ester of phosphoric acid or sulfuric acid.
According to one embodiment of the present invention the electrolyte composition contains at least one further additive (E). If at least one further additive (E) is present, its minimum concentration is usually at least 0.01 wt.-% based on the total weight of the electrolyte composition.
The inventive electrolyte composition preferably is substantially free from water, i.e. the electrolyte composition preferably contains from 0 up to 50 ppm of water, more preferred from 3 to 30 ppm of water and in particular of from 5 to 25 ppm of water. The term “ppm” denotes parts per million based on the weight of the total electrolyte composition.
Various methods are known to the person skilled in the art to determine the amount of water present in the electrolyte composition. A method well suited is the titration according to Karl Fischer, e.g. described in detail in DIN 51777 or ISO760: 1978. “0 ppm water” shall mean, that the amount of water is below the detection limit.
According to one embodiment of the present invention the electrolyte composition contains no components other than the at least one aprotic organic solvent (A), the at least one compound (B), the at least one compound (C), optionally the at least one lithium salt (D), optionally the at least one further additive (E) and 0 to 50 ppm water.
In a preferred embodiment of the present invention the electrolyte composition contains at least two aprotic solvents (A) selected from cyclic and noncyclic organic carbonates (a), at least one compound (B) selected from lithium (bisoxalato) borate, and lithium difluoro (oxalato) borate, and vinylenecarbonate, at least one compound (C) selected from dimethyl methyl phosphonate and at least one lithium salt (D) selected from LiBF4 and LiPF6.
According to a preferred embodiment of the Li ion batteries the electrolyte composition (iii) contains 0.08 to 4 wt.-% of at least one compound (B), and 0.08 to 4 wt.-% of at least one compound (C), more preferred 0.15 to 3 wt.-% of at least one compound (B), and 0.15 to 3 wt.-% of at least one compound (C), based on the weight of the total composition. Electrolytes containing such small amounts of compounds (C) in combination with small amounts of compounds (B) show a beneficial effect on the capacity retention of the Li ion batteries containing said electrolyte composition.
Preference is further given to inventive Li ion batteries comprising electrolyte compositions (iii) containing
The inventive Li ion batteries comprising electrolyte compositions (iii) as described above show increased cycling stability.
In the context of the present invention the term “lithium ion battery” means a rechargeable electrochemical cell wherein during discharge lithium ions move from the negative electrode (anode) to the positive electrode (cathode) and during charge the lithium ions move from the positive electrode to the negative electrode, i.e. the charge transfer is performed by lithium ions. Usually lithium ion batteries comprise a cathode containing as cathode active material a lithium ion-containing transition metal compound, for example transition metal oxide compounds with layer structure like LiCoO2, LiNiO2, and LiMnO2, or transition metal phosphates having olivine structure like LiFePO4 and LiMnPO4, or lithium-manganese spinels which are known to the person skilled in the art in lithium ion battery technology.
The term “cathode active material” denotes the electrochemically active material in the cathode, e.g. the transition metal oxide intercalating/deintercalating the lithium ions during charge/discharge of the battery. Depending on the state of the battery, i.e. charged or discharged, the cathode active material contains more or less lithium ions. The term “anode active material” denotes the electrochemically active material in the anode, e.g. carbon intercalating/deintercalating the lithium ions during charge/discharge of the battery.
According to the present invention the lithium ion batteries comprise a cathode containing a cathode active material selected from lithium ion containing transition compounds having a content of Manganese of from 50 to 100 wt.-%, based on the total weight of transition metal in the lithium ion containing transition metal compound and preferably having a content of Manganese of from 50 to 80 wt.-%. The lithium ion containing transition metal compounds may contain only manganese as transition metal, but may contain manganese and at least one further transition metal or even at least two or three further transition metals.
Lithium ion-containing transition metal oxides containing manganese as the transition metal are understood in the context of the present invention to mean not only those oxides which have at least one transition metal in cationic form, but also those which have at least two transition metal oxides in cationic form. In addition, in the context of the present invention, the term “lithium ion-containing transition metal oxides” also comprises those compounds which—as well as lithium—comprise at least one non-transition metal in cationic form, for example aluminum or calcium.
In a particular embodiment, manganese may occur in cathode in the formal oxidation state of +4. Manganese in cathode more preferably occurs in a formal oxidation state in the range from +3.5 to +4.
According to one embodiment of the present invention the lithium ion batteries have a cell voltage of more than 4.2 V against the anode when fully charged, preferred of at least 4.3 V, more preferred of at least 4.4 V, even more preferred of at least 4.5, most preferred of at least 4.6 V and in particular of at least 4.7 V against the anode when fully charged.
Many elements are ubiquitous. For example, sodium, potassium and chloride are detectable in certain very small proportions in virtually all inorganic materials. In the context of the present invention, proportions of less than 0.1% by weight of cations or anions are disregarded. Any lithium ion-containing mixed transition metal oxide comprising less than 0.1% by weight of sodium is thus considered to be sodium-free in the context of the present invention. Correspondingly, any lithium ion-containing mixed transition metal oxide comprising less than 0.1% by weight of sulfate ions is considered to be sulfate-free in the context of the present invention.
In one embodiment of the present invention, lithium ion-containing transition metal compound is selected from manganese-containing lithium iron phosphates, from manganese-containing spinels and manganese-containing transition metal oxides with layer structure, preferred are manganese-containing spinels and manganese-containing transition metal oxides with layer structure. The manganese-containing transition metal oxides with layer structure may be mixed transition metal oxides comprising not only manganese but at least one further transition metal. In one embodiment of the present invention, lithium ion-containing transition metal compound is selected from those compounds having a superstoichiometric proportion of lithium.
In one embodiment of the present invention, the lithium ion-containing transition metal compound is selected from manganese-containing spinels of the general formula (VI)
Li1+tM2−tO4−d (VI)
wherein
d is 0 to 0.4,
t is 0 to 0.4, and
M is Mn and at least one further transition metal selected from the group consisting of Co and Ni, preferred are combinations of Ni and Mn; or
the lithium ion-containing transition metal compound is selected from manganese containing transition metal oxides with layer structure of general formula (VII)
Li(1+y)[NiaCobMnc](1−y)O2 (VII)
wherein
y is 0 to 0.3, preferably 0.05 to 0.2, and
a, b and c may be same or different and are independently 0 to 0.8 with a+b+c=1.
In one embodiment of the present invention, manganese-containing transition metal oxides with layer structure are selected from those in which [NiaCObMnc] is selected from Ni0.33Co0.33Mn0.33, Ni0.5Co0.2Mn0.3, Ni0.4Co0.3Mn0.4, Ni0.4Co0.2Mn0.4 and Ni0.45Co0.10Mn0.45.
The cathode may comprise one or more further constituents. 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, polyisoprene and copolymers of at least two comonomers selected from ethylene, propylene, styrene, (meth)acrylonitrile and 1,3-butadiene, especially styrene-butadiene copolymers, polyvinylidene fluoride (PVdF), polytetrafluoroethylene, copolymers of tetrafluoroethylene and hexafluoropropylene, copolymers of tetrafluoroethylene and vinylidene fluoride and polyacrylnitrile
Inventive Li ion batteries further comprise at least one anode. In one embodiment of the present invention, the anode contains Li ion intercalating carbon as anode active material. Lithium ion intercalating carbon is known to the person skilled in the art, for example carbon black, so called hard carbon, which means carbon similar to graphite having larger amorphous regions than present in graphite, and graphite, preferred the anode contains graphite, more preferred the anode active material consists essentially of graphite and in particular the anode consists essentially of graphite. The anode may contain further components like binder which may be selected from the binders described above for the cathode.
The inventive lithium ion batteries may contain further constituents customary per se, for example output conductors, separators, housings, cable connections etc. Output conductors may be configured in the form of a metal wire, metal grid, metal mesh, expanded, metal, metal sheet or metal foil. Suitable metal foils are especially aluminum foils. The housing may be of any shape, for example cuboidal or in the shape of a cylinder. In another embodiment, inventive electrochemical cells have the shape of a prism. In one variant, the housing used is a metal-plastic composite film processed as a pouch.
Inventive lithium ion batteries give a high voltage of up to approx. 4.8 V and are notable for high energy density and good stability. More particularly, inventive lithium ion batteries are notable for only a very small loss of capacity in the course of repeated cycling. Several inventive lithium ion 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 automobiles, bicycles operated by electric motor, aircraft, ships or stationary energy stores.
The present invention therefore also further provides for the use of inventive lithium ion batteries 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.
The present invention also further provides a process for producing an inventive lithium ion battery as described above, comprising
Steps (β) to (δ) may be performed in the order described above, but it is also possible to carry out step (γ) before step (β).
The aprotic organic solvent or a mixture of aprotic organic solvents (A) is provided in step (α). The solvent or mixture of solvents (A) may be provided in a dry state, e.g. with a content of water of from 1 to 50 ppm water, based on the weight of (A) or (A) may be provided with a higher content of water. Preferably the aprotic organic solvent or mixture of aprotic organic solvents (A) is provided in liquid form, e.g. when using ethylenecarbonate having a melting point of about 36° C. one or more further solvent (A) like diethylcarbonate and/or methylethylcarbonate are added to obtain a liquid mixture of aprotic organic solvents (A). By addition of diethylcarbonate or methylethylcarbonate the melting point may be lowered. The ratio of different solvents in a mixture of aprotic organic solvents (A) is preferably selected to obtain a mixture being liquid at 0° C. and above. More preferred the ratio of different solvents in a mixture of aprotic organic solvents (A) is selected to obtain a mixture being liquid at −15° C. and above. Whether an aprotic organic solvent or a mixture of aprotic organic solvents (A) is liquid may be determined by visual inspection.
According to one embodiment of the present invention the mixing in steps (β) and (δ) is carried out at temperatures from 10 to 100° C., preferably at room temperature, e.g. at 20 to 30° C. According to another embodiment of the present invention the mixing in steps (β) and (δ) is preferably carried out at a temperature being at least 1° C. above the melting point of that solvent (A) having the highest melting point of all solvents (A) used in the electrolyte composition. The limit of the temperature for mixing is determined by the volatility of that solvent (A) being the most volatile solvent (A) used in the electrolyte composition. Preferably the mixing is performed below the boiling point of the most volatile solvent (A) used in the electrolyte composition.
Mixing is carried out usually under anhydrous conditions, e.g. under inert gas atmosphere or under dried air, preferred mixing is carried out under dried nitrogen atmosphere or dried noble gas atmosphere.
In step (γ) drying is carried out, e.g. by drying the at least one aprotic organic solvent (A) or the at least one mixture of aprotic organic solvents (A) or the mixture obtained so far over at least one ion exchanger or preferably molecular sieve and separating the dried solvent/solvent mixture from ion exchanger or molecular sieve. It is also possible to dry each solvent (A) individually before providing the at least one aprotic organic solvent (A) or the at least one mixture of aprotic organic solvents (A) in step (α), i.e. performing step (γ) before step (α). One embodiment of the present invention comprises performing step (γ) at a temperature in the range from 4 to 100° C., preferably in the range from 15 to 40° C. and more preferably in the range from 20 to 30° C. In one embodiment of the present invention, the time for which ion exchanger or molecular sieve is allowed to act on the solvent mixture is in the range from a few minutes, for example at least 5 minutes, to several days, preferably not more than 24 hours and more preferably in the range from one to 6 hours.
It is preferred to carry out step (γ) before adding any lithium containing compound, e.g. compound (B) or lithium salt (D).
In step (ε) at least one anode and at least one cathode are provided and the lithium ion battery is assembled. This includes the addition of the electrolyte composition (iii). The assembling of lithium ion batteries is known to the skilled person.
The invention is illustrated by the examples which follow, which do not, however, restrict the invention.
Comparative electrolyte composition 1 (CEC 1):
Battery grade solvents ethylene carbonate (EC) and ethyl-(methyl)-carbonate (EMC) were used as solvents (A) at a volume ratio of 3:7. As lithium salt (D) battery grade hexafluorophosphate (LiPF6) was used at a concentration of 1.0 M.
Comparative electrolyte composition 2 (CEC 2):
Lithium bis(oxalato) borate (LiBOB) was purchased from Chemetall. To electrolyte CEC 1 (1.0 M LiPF6 EC/EMC (3/7, v/v)) 0.5 wt.-% LiBOB, and 1 wt.-% vinylene carbonate (VC) were added.
Comparative electrolyte composition 3 (CEC 3):
Dimethyl methylphosphonate (DMMP) was distilled and soaked with 4 Å molecule seizes before use. 1 wt.-% of DMMP was added to the electrolyte composition CEC 1.
Comparative electrolyte composition 4 (CEC 4):
Lithium bis(oxalato) borate (LiBOB) was purchased from Chemetall. 0.5 wt.-% of LiBOB was added to the electrolyte composition CEC 1.
Inventive electrolyte composition 1 (IEC 1):
Dimethyl methylphosphonate (DMMP) was distilled and soaked with 4 Å molecule seizes before use. DMMP and LiBOB were added to electrolyte CEC 1 (1.0 M LiPF6 EC/EMC (3/7, v/v)) yielding an inventive electrolyte composition containing 1 wt.-% of DMMP and 0.5 wt.-% LiBOB.
Inventive electrolyte composition 2 (IEC 2):
Dimethyl methylphosphonate (DMMP) was distilled and soaked with 4 Å molecule seizes before use. Vinylenecarbonate (VC) and DMMP were added to electrolyte CEC 1 (1.0 M LiPF6 EC/EMC (3/7, v/v)) yielding concentrations of 0.5 wt.-% VC and 1 wt.-% DMMP.
Inventive electrolyte composition 3 (IEC 3):
IEC 3 was prepared as IEC-1 with the difference that lithium difluoro oxalato borate (LiDFOB) was used instead of LiBOB.
B) Dissolution of Transition Metal from LiNi0.5Mn1.5O4
LiNi0.5Mn1.5O4 powder was provided by BASF. The samples for thermal storage were prepared in a high purity argon filled glove-box. The vials were charged with 0.1 g LiNi0.5Mn1.5O4 powder followed by addition of 2 mL CEC1 and IEC 1, respectively. The vials were flame sealed under reduced pressure. Care was given to avoid contamination of the vial walls near the sealing point. The sealed samples were stored at 55° C. for 2 weeks. Samples were weighted before and after thermal storage to confirm seal. After thermal storage, vials were opened in an argon filled glove-box. The solid LiNi0.5Mn1.5O4 samples were separated from the respective electrolyte and then washed with dimethyl carbonate (DMC) three times followed by drying in vacuum. The residual electrolyte solutions were analyzed by ICP-MS (inductively-coupled-plasma mass-spectrometry) to determine the content of Mn and Ni. The results are shown in table 2.
The cathode electrode was composed of 89% LiNi0.5Mn1.5O4, 6% conductive carbon, and 5% PVDF. 2032-type coin cells were assembled with a graphite anode, the LiNi0.5Mn1.5O4 cathode, and a Celgard 2325 separator. Each cell contained 30 μL electrolyte composition. The cells were cycled with a constant current-constant voltage charge and constant current discharge between 3.5 to 4.9 V with Arbin BT2000 cycler according to following protocol: 1st cycle at C/20; 2nd and 3rd cycles at C/10; remaining cycles at C/5. 50 cycles were performed at room temperature, followed by 20 cycles at 55° C. All cells were produced in triplicate and representative data is provided. The results are shown in table 3
At room temperature the cells with inventive electrolyte compositions showed better cycling performance, discharge capacity and coulombic efficiency than cells comprising comparative electrolytes.
In table 4 the cycling performance of cells with CEC 1, CEC 3, CEC 4 and IEC1 at room temperature are shown. The cycling protocol was the same as described above.
As can be seen in table 4, the inventive combination of LiBOB and DMMP shows higher capacity retention than the electrolyte composition without additives and than the electrolyte compositions containing only one of the respective additives at room temperature.
| Number | Date | Country | Kind |
|---|---|---|---|
| 12177345.1 | Jul 2012 | EP | regional |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14412811 | Jan 2015 | US |
| Child | 16834686 | US |
