ADDITIVES FOR ELECTROLYTE AND CATHODE MATERIAL IN Li-ION BATTERIES COMPRISING METAL-BASED CATHODE MATERIAL WHICH PRODUCES M2+ METAL IONS

Abstract

Method of improving the performance of a Li-ion battery comprising metal-based cathode material which produces M.sup.2+ metal ions. The method comprises using a small organic compound in association with the electrolyte of the battery or using a polymer compound in association with the cathode active material of the battery. The small organic compound and the polymer compound comprise at least one chemical group suitable for forming complexes with the M.sup.2+ metal ions thereby preventing dissolution thereof.

Claims

1. A method of improving the performance of a Li-ion battery comprising metal-based cathode material which produces M.sup.2+ metal ions, the method comprising using a small organic compound in association with the electrolyte of the battery, wherein the small organic compound comprises at least one chemical group suitable for forming complexes with the M.sup.2+ metal ions thereby preventing dissolution thereof.

2. A method for preventing metal ions dissolution in a Li-ion battery comprising metal-based cathode material which produces M.sup.2+ metal ions, the method comprising using a small organic compound in association with the electrolyte of the battery, wherein the small organic compound comprises at least one chemical group suitable for forming complexes with the M.sup.2+ metal ions.

3. The method according to claim 1 or 2, wherein the M.sup.2+ metal ions are selected from the group consisting of: Mn.sup.2+, Fe.sup.2+, Ca.sup.2+ and other divalent metal ions; preferably the metal-based cathode material is an Mn-based cathode material.

4. The method according to claim 1 or 2, wherein the small organic compound is added to the electrolyte.

5. The method according to any one of claims 1 to 4, wherein the small organic compound has a general formula I outlined below ##STR00015## wherein: Q is a 5 to 12-member ring or bicycle ring, optionally the ring comprises one or more heteroatom which are the same or different; Ri and R′i are each independently selected from H, alkyl, cycloalkyl, alkene, alkyne, aryl and alkylaryl, alkoxy, thioalkoxy, OH, SH, NH.sub.2, a halogen atom, a halogeno alkyl, a halogeno alkoxy, a halogeno thioalkoxy, a cyano alkyl, a cyano alkene, a cyano alkyne, CN, NO.sub.2, SO.sub.2, COOH and acyloxycarbonyl, with the proviso that at least one of Ri and R′i comprises a heteroatom; n and m are each independently an integer from 0 to 11, with the proviso that they are not both 0 at the same time; and the heteroatom is selected from O, S and N.

6. The method according to claim 5, wherein at least two of Ri and R′i comprise a heteroatom, and the at least two of Ri and R′i are attached to consecutive carbon atoms of the ring; or when Q is a bicycle ring the at least two of Ri and R′i are spatially close to each other.

7. The method according to claim 5 or 6, wherein the small organic compound has a general formula II outlined below ##STR00016## wherein: Ri and R′i are as defined in claim 5, and are both different from H; and n and m are as defined in claim 5, and n=2-4 or n=2 and m=1.

8. The method according to claim 5 or 6, wherein the small organic compound has a general formula III outlined below ##STR00017## wherein R.sub.1, R.sub.2 and R′ are each as defined in claim 7 for Ri and R′i.

9. The method according to claim 5 or 6, wherein the small organic compound has a general formula IV outlined below ##STR00018## wherein R.sub.1, R.sub.2 and R′ are each as defined in claim 7 for Ri and R′i.

10. The method according to claim 5 or 6, wherein the small organic compound has a general formula V outlined below ##STR00019## wherein: R′ is as defined in claim 6 for Ri and R′i; R.sub.3 and R.sub.4 are each independently H or a 01-6 alkyl; and X.sub.1 and X2 are each independently a heteroatom, preferably the heteroatom is O, S or N, more preferably the heteroatom is O.

11. The method according to claim 5 or 6, wherein the small organic compound is selected from Compound A, Compound B, Compound C, and Compound D outlined below ##STR00020##

12. An electrolyte comprising the small organic compound as defined in any one of claims 1 to 11.

13. A battery comprising the electrolyte as defined in claim 12.

14. A polymer compound having a general formula VI outlined below ##STR00021## wherein: Q and Q′ are each independently a 5 to 12-member ring or bicycle ring, optionally the ring comprises one or more heteroatom which are the same or different; L a linker comprising alkyl groups; Ri and R′i are each independently selected from H, alkyl, cycloalkyl, alkene, alkyne, aryl and alkylaryl, alkoxy, thioalkoxy, OH, SH, NH.sub.2, a halogen atom, a halogeno alkyl, a halogeno alkoxy, a halogeno thioalkoxy, a cyano alkyl, a cyano alkene, a cyano alkyne, CN, NO.sub.2, SO.sub.2, COOH and acyloxycarbonyl, with the proviso that at least one of Ri comprises a heteroatom and at least one of R′i is different from H; n and m are each independently an integer from 0 to 11 with the proviso that they are not both 0 at the same time; and the heteroatom is selected from O, S and N.

15. The polymer according to claim 14, wherein at least two of Ri comprise a heteroatom, and the at least two of Ri are attached to consecutive carbon atoms of the ring; or when Q is a bicycle ring the at least two of Ri are spatially close to each other.

16. The polymer according to claim 14 or 15, wherein the at least one R′i is a halogen atom, preferably F.

17. A polymer compound having a general formula VII outlined below ##STR00022## wherein: L is as defined in claim 14; Ri is as defined in claim 15; R′i is as defined in claim 16; and n and m are each as defined in claim 14.

18. A polymer compound having a general formula VIII outlined below ##STR00023## wherein: both R.sub.1 and R.sub.2 comprise a heteroatom; R′.sub.1-5 are each as defined in claim 16 for R′i; and L is as defined in claim 14.

19. The polymer according to claim 18, wherein both R.sub.1 and R.sub.2 comprise a heteroatom, and are attached to consecutive carbon atoms of the ring.

20. A polymer compound having a general formula IX outlined below ##STR00024## wherein: R.sub.3, R.sub.4 and R.sub.6-9 are each independently H or a 01-6 alkyl; R′.sub.1-5 are each as defined in claim 18; L′ is as defined in claim 14 for L, preferably L′ is constituted of repeating units of CR.sub.6R.sub.7 and CR.sub.8R.sub.9; and X.sub.1 and X2 are each independently a heteroatom, preferably the heteroatom is O, S or N, more preferably the heteroatom is O.

21. A polymer having a formula P outlined below ##STR00025##

22. A polymer having a formula P′ outlined below ##STR00026##

23. A polymer of formula P, which comprises 48 mol % of dimethoxystyrene moities (Polymer dimethoxy-1).

24. A polymer of formula P, which comprises 70 mol % of dimethoxystyrene moities (Polymer dimethoxy-2).

25. A polymer of formula P, which comprises 100 mol % of dimethoxystyrene moities (Polymer dimethoxy-3).

26. A polymer of formula P′, which comprises 50 mol % of dihydroxystyrene moities (Polymer difydroxy-1).

27. A method of improving the performance of a Li-ion battery comprising metal-based cathode material which produces M.sup.2+ metal ions, the method comprising using a polymer compound in association with the cathode material of the battery, wherein the polymer compound comprises at least one chemical group suitable for forming complexes with the M.sup.2+ metal ions thereby preventing dissolution thereof.

28. A method of preventing metal ions dissolution in a Li-ion battery comprising metal-based cathode material which produces M.sup.2+ metal ions, the method comprising using a polymer compound in association with the cathode of the battery, wherein the polymer compound comprises at least one chemical group suitable for forming complexes with the M.sup.2+ metal ions.

29. The method according to claim 27 or 28, wherein the M.sup.2+ metal ions are selected from the group consisting of: Mn.sup.2+, Fe.sup.2+, Ca.sup.2+ and other divalent metal ions; preferably the metal-based cathode material is an Mn-based cathode material.

30. The method according to any one of claims 27 to 29, wherein the polymer compound is added to the cathode material.

32. A method of preventing metal ions dissolution in a Li-ion battery comprising metal-based cathode material which produces M.sup.2+ metal ions, the method comprising using a polymer compound in association with the cathode material of the battery, wherein the polymer compound is as defined in any one of claims 14 to 26.

33. A cathode material comprising the polymer compound as defined in any one of claims 14 to 26.

34. A battery comprising the cathode material as defined in claim 33.

35. A method for preparing the polymer compound as defined in any one of claims 14 to 26, comprising submitting a dialkyloxystyrene compound and a pentahalogenostyrene compound to a random copolymerization to obtain an alkyoxystyrene polymer; and optionally submitting the alkyoxystyrene polymer to a dealkylation process to obtain a hydroxy polymer compound.

36. The method according to claim 35, wherein the dialkyloxystyrene compound is di methoxystyrene, and the pentahalogenostyrene compound is pentafluorostyrene.

37. A method for preparing a polymer compound of formula P, comprising submitting di methoxystyrene and pentafluorostyrene to a random copolymerization.

38. A method for preparing a polymer compound of formula P′, comprising submitting the polymer compound of formula P to a demethylation process.

39. A method for preparing the polymer compound as defined in any one of claims 14 to 26, comprising submitting a dialkyloxystyrene compound and a pentahalogenostyrene compound to a polymerization process which is atom transfer radical polymerization (ATRP), atom transfer radical addition polymerization (ATRAP), retarded anionic polymerization (RAP), cationic polymerization or the like.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0014] The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.

[0015] In the appended drawings:

[0016] FIG. 1: Charge-Discharge curves of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.5% additive according to the invention (Compound A)) versus Reference.

[0017] FIG. 2: Charge-Discharge curves of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.5% additive according to the invention (Compound A)) versus Reference, at 0.05 C at various cycles (0, 100, 200 and 300 cycles).

[0018] FIG. 3: Nyquist plots of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.5% additive according to the invention (Compound A)) versus Reference, at various cycles (0, 100, 200 and 300 cycles).

[0019] FIG. 4: Cycling data of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.5% additive according to the invention (Compound A)) versus Reference after 300 cycles at 45° C.

[0020] FIG. 5: Charge-Discharge curves of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.1% additive according to the invention (Compound B)) versus Reference.

[0021] FIG. 6: Conductivities of electrolytes, PC/EMC/DMC (4/3/3)+1M LiPF.sub.6 versus PC/EMC/DMC (4/3/3)+1M LiPF6+0.1% of additive according to the invention (Compound B).

[0022] FIG. 7: Charge-Discharge curves of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.1% additive according to the invention (Compound B)) versus Reference, at 0.05 C at various cycles (0, 100 and 200).

[0023] FIG. 8: Cycling data of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.1% additive according to the invention (Compound B)) versus Reference after 303 cycles at 45° C.

[0024] FIG. 9: Charge-Discharge curves of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.1% additive according to the invention (Compound C)) versus Reference.

[0025] FIG. 10: Cycling data of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.1% additive according to the invention (Compound C)) versus Reference after 300 cycles at 45° C.

[0026] FIG. 11: Nyquist plots of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.1% additive according to the invention (Compound C)) versus Reference, at 300 cycles.

[0027] FIG. 12: Charge-Discharge curves of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.1% additive according to the invention (Compound D)) versus Reference.

[0028] FIG. 13: Cycling data of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.1% additive according to the invention (Compound D)) versus Reference after 300 cycles at 45° C.

[0029] FIG. 14: Nyquist plots of LMFP-LTO battery (PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+0.1% additive according to the invention (Compound D)) versus Reference, at 300 cycles.

[0030] FIG. 15: Cycling data of (LMFP+4% PVDF+1% additive (binder) according to the invention (polymer comprising 48 mol % dimethoxystyrene moieties or “Polymer dimethoxy-1”)-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC) battery versus Reference (LMFP+5% PVDF-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC) after 325 cycles at 45° C.

[0031] FIG. 16: Charge-Discharge curves of (LMFP+4% PVDF+1% additive (binder) according to the invention (polymer comprising 48 mol % dimethoxystyrene moieties or “Polymer dimethoxy-1”)-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC) battery versus Reference (LMFP+5% PVDF-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC).

[0032] FIG. 17: Cycling data of (LMFP+4% PVDF+1% additive (binder) according to the invention (polymer comprising 70 mol % dimethoxystyrene moieties or “Polymer dimethoxy-2”)-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC) battery versus Reference (LMFP+4% PVDF-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC), after 300 cycles at 45° C.

[0033] FIG. 18: Cycling data of (LMFP+4% PVDF+1% additive (binder) according to the invention (polymer comprising 100 mol % dimethoxystyrene moieties or “Polymer dimethoxy-3”)-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC) battery versus Reference (LMFP+4% PVDF-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC), after 300 cycles at 45° C.

[0034] FIG. 19: Cycling data of (LMFP+4% PVDF+1% additive (binder) according to the invention (polymer comprising 50 mol % dihydroxystyrene moieties or “Polymer dihydroxy-1”)-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC) battery versus Reference (LMFP+4% PVDF-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC), after 300 cycles at 45° C.

[0035] FIG. 20: Nyquist plots of (LMFP+4% PVDF+1% additive (binder) according to the invention (polymer comprising 50 mol % dihydroxystyrene moieties or “Polymer dihydroxy-1”)-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC) battery versus Reference (LMFP+4% PVDF-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC).

[0036] FIG. 21: Capacities of (LMFP+4% PVDF+1% additive (binder) according to the invention (polymer comprising 50 mol % dihydroxystyrene moieties or “Polymer dihydroxy-1”)-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC) battery versus Reference (LMFP+4% PVDF-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC); A) Charge B) Discharge.

[0037] FIG. 22: Charge-Discharge of (LMFP+4% PVDF+1% additive (binder) according to the invention (polymer comprising 50 mol % dihydroxystyrene moieties or “Polymer dihydroxy-1”)-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC) battery versus Reference (LMFP+4% PVDF-LTO-PC/EMC/DMC (4/3/3)+1M LiPF.sub.6+1% VC).

DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

[0038] Before the present invention is further described, it is to be understood that the invention is not limited to the particular embodiments described below, as variations of these embodiments may be made and still fall within the scope of the appended claims. It is also to be understood that the terminology employed is for the purpose of describing particular embodiments; and is not intended to be limiting. Instead, the scope of the present invention will be established by the appended claims.

[0039] In order to provide a clear and consistent understanding of the terms used in the present specification, a number of definitions are provided below. Moreover, unless defined otherwise, all technical and scientific terms as used herein have the same meaning as commonly understood to one of ordinary skill in the art to which this disclosure pertains.

[0040] The use of the word “a” or “an” when used in conjunction with the term “comprising” in the claims and/or the specification may mean “one”, but it is also consistent with the meaning of “one or more”, “at least one”, and “one or more than one”. Similarly, the word “another” may mean at least a second or more.

[0041] As used in this specification and claim(s), the words “comprising” (and any form of comprising, such as “comprise” and “comprises”), “having” (and any form of having, such as “have” and “has”), “including” (and any form of including, such as “include” and “includes”) or “containing” (and any form of containing, such as “contain” and “contains”), are inclusive or open-ended and do not exclude additional, unrecited elements or process steps.

[0042] As used herein when referring to numerical values or percentages, the term “about” includes variations due to the methods used to determine the values or percentages, statistical variance and human error. Moreover, each numerical parameter in this application should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques.

[0043] Term “alkyl” or “alk” as used herein, represents a monovalent group derived from a straight or branched chain saturated hydrocarbon comprising, unless otherwise specified, from 1 to 15 carbon atoms and is exemplified by methyl, ethyl, n- and iso-propyl, n-, sec-, iso- and tert-butyl, neopentyl and the like and may be optionally substituted with one, two, three or, in the case of alkyl groups comprising two carbons or more, four substituents.

[0044] The term “alkoxy” or “alkyloxy” as used interchangeably herein, represents an alkyl group attached to the parent molecular group through an oxygen atom.

[0045] The term “alkylthio” or “thioalkoxy” as used interchangeably herein, represents an alkyl group attached to the parent molecular group through a sulfur atom.

[0046] The term “alkylene” as used herein, represents a saturated divalent hydrocarbon group derived from a straight or branched chain saturated hydrocarbon by the removal of two hydrogen atoms, and is exemplified by methylene, ethylene, isopropylene and the like.

[0047] The term “alkenyl” as used herein, represents monovalent straight or branched chain groups of, unless otherwise specified, from 2 to 15 carbons, such as, for example, 2 to 6 carbon atoms or 2 to 4 carbon atoms, containing one or more carbon-carbon double bonds and is exemplified by ethenyl, 1-propenyl, 2-propenyl, 2-methyl-1-propenyl, 1-butenyl, 2-butenyl and the like and may be optionally substituted with one, two, three or four substituents.

[0048] The term “alkynyl” as used herein, represents monovalent straight or branched chain groups of from two to six carbon atoms comprising a carbon-carbon triple bond and is exemplified by ethynyl, 1-propynyl, and the like and may be optionally substituted with one, two, three or four substituents.

[0049] The term “cycloalkyl” as used herein, represents a monovalent saturated or unsaturated non-aromatic cyclic hydrocarbon group of three to eight carbon atoms, unless otherwise specified, and is exemplified by cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, bicyclo[2.2.1]heptyl and the like.

[0050] The term “halogen” or “halo” as used interchangeably herein, represents F, Cl, Br and I.

[0051] The term “heteroatom”, as used herein, is understood as being oxygen, sulfur or nitrogen.

[0052] The inventors have designed and prepared an additive for use in association with the electrolyte in a Li-ion battery comprising a metal-based cathode material capable of producing M.sup.2+ metal ions. The additive of the invention is added to the electrolyte; and allows for the prevention of the M.sup.2+ ions dissolution.

[0053] More specifically, the additive of the invention for use in association with the electrolyte is a small organic molecule as described herein and having general formulae I-V. Such small organic compounds are exemplified by Compounds A-D. The small organic compound comprises at least one chemical group suitable for forming complexes with the M.sup.2+ metal ions. Such chemical group are apparent to a skilled person. Also, the small organic compound is compatible with the electrolyte as well as other components of the battery.

[0054] Also, the inventors have designed and prepared an additive (binder) for use in association with the cathode material in a Li-ion battery comprising a metal-based cathode material capable of producing M.sup.2+ metal ions. The additive according to this aspect of the invention is a binder. The binder is mixed with the cathode material; and allows for the prevention of the M.sup.2+ ions dissolution.

[0055] More specifically, the additive or binder of the invention for use in association with the cathode material is a polymer compound as described below and having general formulae VI-IX. Such polymer compounds are exemplified by Polymer P and Polymer P′. The polymer compound comprises at least one chemical group suitable for forming complexes with the M.sup.2+ metal ions. Such chemical group are apparent to a skilled person. Also, the polymer compound is compatible with the cathode active material as well as other components of the battery.

[0056] The present invention is illustrated in further details by the following non-limiting examples.

Small Organic Molecule for Use as Additive in Association with the Electrolyte

[0057] Example 1—Preparation of Compound A: 3,4-dimethoxybenzaldehyde (1 equivalent) and malanonitrile (1.5 equivalent) were solubilized in chloroform. Under stirring, 3 drops of trimethylamine were added. After 1 night at 60° C., the solvent was evaporated. The crude was washed with water 3 times and extracted by dichloromethane. The organic phases were dried with MgSO.sub.4 and the solvent evaporated. The orange solid was purified by gel chromatography (eluent: hexanes:dichloromethane (80:20)) to give light yellow solid (70%).

[0058] Compound B, Compound C and Compound D are commercially available and were used as received.

Polymer Compound for Use as Additive (Binder) in Association with the Cathode Material

[0059] The polymer compound according to the invention is obtained from pentafluorostyrene and dimethoxystyrene as outlined in Scheme 1 below. Pentafluorostyrene allows for a good compatibility with PVDF and a good electrochemical stability. The level of incorporation of dimethoxystyrene in the polymer according to the invention is around 40 mol % or higher. In this regard, Polymer dimethoxy-1 (polymer comprising 48 mol % of dimethoxystyrene moities), Polymer dimethoxy-2 (polymer comprising 70 mol % of dimethoxystyrene moities) and Polymer dimethoxy-3 (polymer comprising 100 mol % of dimethoxystyrene moities) were prepared as outlined at Example 2 below. The preparation is generally based on a random copolymerization of dimethoxystyrene (DMSt) and pentafluorostyrene (PFS). Dimethoxystyrene forms a complex with the metals ions including Mn.sup.2+ ions, therefore limiting their diffusion throughout the electrolyte, and thus their deposition on the anode side.

##STR00013##

[0060] The polymer compound of the invention with free hydroxy groups (polymer comprising dihydroxystyrene moieties) is obtained as outlined in Scheme 2. In this regard, Polymer dihydroxy-1 (polymer comprising 50 mol % of dihydroxystyrene moities) was prepared.

##STR00014##

[0061] Example 2—Preparation of Polymer dimethoxy-1: DMSt and PFS were first passed through basic aluminum oxide (alumina, Al.sub.2O.sub.3). Polymerization was achieved by introducing 50 mL of dioxane, 3.2 g of DMSt and 3.7 g of PFS into a 100 mL round bottom flask. The solution was then stirred with a magnetic bar for 30 minutes and bubbled with nitrogen (N.sub.2). 80 mg of AIBN was then added to the obtained solution. A condenser was then attached to the round bottom flask and the reaction mixture was heated at 80° C. for 12 hours under N2. The resulting solution was then cooled down to room temperature and poured in 10 volumes of methanol. The supernatant was separated from the precipitated polymer, which was then dried under vacuum at 60° C. for 12 hours. Yield=4.1 g, 48 mol % in DMSt, M.sub.n=26 000 g/mol, PDI=1.7.

[0062] As will be understood by a skilled person, Polymer dimethoxy-2 and Polymer dimethoxy-3 are prepared by the same procedure described in Example 2.

[0063] Example 3—Preparation of a polymer comprising dihydroxystyrene moieties (Polymer dihydroxy-1): Polymer dimethoxy-2 or 3 obtained in Example 2 was subjected to hydrolysis according to a method described by Westwood et al. [6], 0.50 g of Polymer dimethoxy-2 or 3 and 4.3 mL of BBr.sub.3 in DCM 1.0M were used.

[0064] Example 4—Preparation of the cathode material according to the invention: the hybrid cathode pastes were prepared by mechanically mixing (thinky Mixer SR-500) of additives if present, active material, acetylene black (Denka HS-100L), carbon fiber (VGCF-SDH-HC) and PVDF (130 mg/mol) in NMP. The resulting viscous slurry was cast by the doctor Blade method uniformly onto an aluminum foil serving as a current collector, dried at 80° C. under vacuum and roll-pressed with Rolling Machine (MSK-2150) at 63 μm to achieve an electrode active layer density 8.5 mg/cm.sup.2. Electrodes were further dried under vacuum at 150° C. before use.

[0065] As will be understood by a skilled person, the polymer according to the invention may be prepared by different polymerization processes, such processes include but are not limited to atom transfer radical polymerization (ATRP), atom transfer radical addition polymerization (ATRAP), retarded anionic polymerization (RAP), cationic polymerization or the like.

[0066] Referring to the figures, FIGS. 1-4 outline results obtained using Compound A as additive in the electrolyte. As can be seen in FIG. 2, at the beginning of the cycling process, metals ions dissolution decreases, and this continues during the whole cycling process. Indeed, the plateau related to the metals for the Reference decreases, and the phenomenon is less important for the battery according to the invention, namely, the battery wherein the electrolyte comprises Compound A as additive. Moreover, during the cycling process, the internal resistance of the battery according to the invention remains the same as in the Reference, whereas the resistance associated to charge transfer decreases significantly.

[0067] As can be seen in FIG. 3 and FIG. 4, after 300 cycles at 10 and 45° C., the retention capacity of the battery comprising 0.5% of Compound A as additive is 61%, whereas it is 50% for the Reference. After 300 cycles, the static capacity at 0.05 C of the battery according to the invention is 1.80 mAh, whereas it is 1.30 mAh for the Reference.

[0068] Compound B was also used as additive in the electrolyte. The results obtained are outlined in FIGS. 5-8. The capacity at 0.2 C of the battery LMF/LTO with 0.1% of Compound B as additive is 2.48 mAh, the same as in the Reference. As can be seen, the use of 0.1% of Compound B as additive improves the conductivity and enhances the performances of the battery at various C-rates. It can also be seen that metals ions dissolution decreases right at the beginning of the cycling process.

[0069] As can be seen in FIG. 7 and FIG. 8, after 300 cycles at 10 and 45° C., the retention capacity of the battery comprising 0.1% of Compound B as additive is 62%, whereas it is 50% for the Reference. After 300 cycles, the static capacity at 0.05 C of the battery according to the invention is 1.92 mAh, whereas it is 1.64 mAh for the Reference.

[0070] Compound C and Compound D were also used as additive in the electrolyte. The results obtained are outlined in FIGS. 9-14. Referring to FIG. 9, although a secondary reaction is observed, the capacity obtained is similar to the one obtained for the Reference. As can be seen in FIG. 12, a secondary reaction is observed, which leads to a slight irreversibility. Nonetheless, the capacity obtained is similar to the one obtained for the Reference.

[0071] Referring to FIGS. 15-18, the capacity for LMFP (4% PVDF, 1% Polymer dimethoxy-1, 2 or 3-LTO at 0.2 C is 2.23 mAh, while the capacity is 2.35 mAh for the LMFP (5% PVDF)-LTO. After 350 cycles at 45° C. and 1 C, the retention capacity of 61.9% with 1% of additive while the control is at 45.9%. Moreover, static capacities (0.2 C) are 1.53 and 1.23 mAh after 350 cycles, respectively. Also, voltage fading is reduced after 350 cycles (FIG. 16); the capacity of the Reference is 1.23 mAh, the capacity of the battery according to the invention is 1.53 mAh.

[0072] Referring to FIGS. 19-22, the polymer comprising dihydroxystyrene moieties is also used for complexation. FIG. 18 shows the capacity retention when Polymer dihydroxy-1 (polymer comprising 50 mol % dihydroxystyrene moieties) is used. No major improvement is observed. However, as can be seen in FIG. 20, a decrease of the resistance of the material is observed after 300 cycles. It should be noted that before cycling no major difference is noted between the Reference and the battery according to the invention. Capacities recorded after 300 cycles are higher when the additive (binder) according to the invention is used. The charge/discharge at various C-rates shows a good improvement at 2 C.

[0073] As will be understood by a skilled person, the additive for use in association with the electrolyte and the additive (binder) for use in association the cathode active material are adapted to be compatible with the components of the battery including the electrolyte and the cathode active material.

[0074] The scope of the claims should not be limited by the preferred embodiments set forth in the examples; but should be given the broadest interpretation consistent with the description as a whole.

[0075] The present description refers to a number of documents, the content of which is herein incorporated by reference in their entirety.

REFERENCES

[0076] 1. D. Mohanty, J. Li, D. P. Abraham, A. Huq, E. A. Payzant, D. L. Wood, C. Daniel, Chemistry of Materials, 26 (2014) 6272-6280. [0077] 2. M. Saulnier, A. Auclair, G. Liang, S. B. Schougaard, Solid State Ionics, 294 (2016) 1-5. [0078] 3. Z. Shiming, G. Haitao, P. Hongge, Y. Suhui, D. Wubin, L. Xiang, G. Mingxia, L. Yongfeng, Z. Min, O. Liuzhang, J. Dechao, P. Feng, Advanced Energy Materials, 7 (2017) 1601066. [0079] 4. A. Tomheim, M. He, C.-C. Su, Z. Zhang, Journal of the Electrochemical Society, 164 (2017) A6366-A6372. [0080] 5. U.S. Pat. Nos. 5,846,673; 7,749,660; 10,008,749. [0081] 6. G. Westwood, T. N. Horton, J. J. Wilker, Macromolecules, 40 (2007) 3960-3964. [0082] 7. Z. Xu, Scientific Reports, 3 (2013) 2914.