IP Library Granted Patent US 7,638,243
Granted Patent B2
US 7,638,243 · App. 11/387,142 · Granted Dec 29, 2009

Stabilized nonaqueous electrolytes for rechargeable batteries

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Quick Facts
Patent No.
US 7,638,243
App. No.
11/387,142
Granted
Dec 29, 2009
Kind
B2
Abstract

The invention relates to the use of aromatic phosphite compounds as stabilizers for nonaqueous electrolytic solutions containing halogenated salts such as LiPF 6 and LiBF 4 . The electrolyte containing such a phosphite exhibits excellent shelf life storage at ambient and high temperatures. The electrolytic solution is suitable for use in electrochemical cells such as lithium (ion) rechargeable batteries and supercapacitors.

Claims (25)

1. A secondary battery comprising

a. an anode,

b. a cathode comprising lithium, and

c. an electrolytic solution comprising

i. a non-aqueous solvent,

ii. a solute, and

iii. about 0.01 wt % to about 5 wt % of an aromatic phosphite compound selected from the group consisting of tris(p-fluorophenyl) phosphite), tris(perfluorophenyl) phosphite, di(p-fluorophenyl) phenyl phosphite, and di(perfluorophenyl) phenyl phosphite.

2. The secondary battery of claim 1 comprising about 0.05 to about 3 wt % of the aromatic phosphite compound.

3. The secondary battery of claim 1 comprising about 0.1 to about 2 wt % of the aromatic phosphite compound.

4. The secondary battery of claim 1 wherein the solute is present in a concentration of about 0.1 to about 2.5 M and is selected from the group consisting of LiPF 6 , LiBF 4 , LiClO 4 , LiAsF 6 , LiTaF 6 , LiAlCl 4 , LiCF 3 SO 3 , Li 2 B 10 Cl 10 , Li 2 B 10 F 10 , Li 2 B 12 H x F (12-x) LiBF y (R F ) 4-y , LiPF z (R F ) 6-z , LiBF 2 [C 2 O 4 (CE 2 ) w ], LiPF 2 [C 2 O 4 (CE 2 ) w ] 2 , LiPF 4 [C 2 O 4 (CE 2 ) w ], LiN(SO 2 C m F 2m+1 )(SO 2 C n F 2n+1 ), LiC(SO 2 C k F 2k+1 )(SO 2 C m F 2m+1 )(SO 2 C n F 2n+1 ), LiN(SO 2 C p F 2p SO 2 ), and LiC(SO 2 C p F 2p SO 2 )(SO 2 C q F 2q+1 ), wherein E is H, F, or Cl; wherein R F is a perfluorinated C 1 -C 20 alkyl group or perfluorinated aromatic group, wherein 1≦k, m, n, p, q, ≦10; 0≦w ≦4; 0≦x≦12; 0≦y≦3; and 0≦z≦5.

5. The secondary battery of claim 1 wherein the non-aqueous solvent is selected from the group consisting of ethylene carbonate, propylene carbonate, butylene carbonate, dimethyl carbonate, diethyl carbonate, dipropyl carbonate, dibutyl carbonate, ethyl methyl carbonate, methyl propyl carbonate, ethyl propyl carbonate, tetrahydrofuran, 2-methyl tetrahydrofuran, 1,3-dioxolane, 1,4-dioxane, 1,2-dimethoxyethane, 1,2-diethoxyethane, 1,2-dibutoxyethane, acetonitrile, dimethylformamide, methyl formate, ethyl formate, propyl formate, butyl formate, methyl acetate, ethyl acetate, propyl acetate, butyl acetate, methyl propionate, ethyl propionate, propyl propionate, butyl propionate, methyl butyrate, ethyl butyrate, propyl butyrate, butyl butyrate, γ-butyrolactone, 2-methyl- γ-butyrolactone, 3-methyl- γ-butyrolactone, 4-methyl- γ-butyrolactone, β-propiolactone, δ-valerolactone, trimethyl phosphate, triethyl phosphate, tris(2-chloroethyl) phosphate, tris(2,2,2-trifluoroethyl) phosphate, tripropyl phosphate, triisopropyl phosphate, tributyl phosphate, trihexyl phosphate, triphenyl phosphate, tritolyl phosphate, and combinations thereof.

6. The secondary battery of claim 1 wherein the cathode comprises a lithium mixed metal oxide selected from the group consisting of LiMnO 2 , LiMn 2 O 4 , LiCoO 2 , Li 2 Cr 2 O 7 , Li 2 CrO 4 , LiNiO 2 , LiFeO 2 , LiNi x Co 1-x O 2 (0<x<1), LiFePO 4 , LiMn 0.5 Ni 0.5 O 2 , LiMn x Co y Ni z O 2 wherein 0<x,y,z<1, and LiMc 0.5 Mn 15 O 4 wherein Mc is a divalent metal, and mixtures thereof.

7. The secondary battery of claim 1 , wherein the anode comprises a material selected from the group consisting of crystalline carbon, lithium metal, LiMnO 2 , LiAl, LiZn, Li 3 Bi, Li 3 Cd, Li 3 Sb, Li 4 Si, Li 4.4 Pb, Li 4.4 Sn, LiC 6 , Li 3 FeN 2 , Li 2.6 Co 0.4 N, Li 2.6 Cu 0.4 N, Li 4 Ti 5 O 12 , and combinations thereof.

8. The secondary battery of claim 7 , wherein the anode further comprises a material selected from the group consisting of SnO, SnO 2 , GeO, GeO 2 , In 2 O, In 2 O 3 , PbO, PbO 2 , Pb 2 O 3 , Pb 3 O 4 , Ag 2 O, AgO, Ag 2 O 3 , Sb 2 O 3 , Sb 2 O 4 , Sb 2 O 5 , SiO, ZnO, CoO, NiO, FeO, and combinations thereof.

9. The secondary battery of claim 7 , wherein the anode further comprises a binder selected from the group consisting of polyvinylidene fluoride, styrene-butadiene rubber, polyamide, melamine, and combinations thereof.

10. The secondary battery of claim 1 further comprising a salt additive selected from the group consisting of chelated orthoborate salts and chelated orthophosphate salts.

11. The secondary battery of claim 10 wherein the salt additive is selected from the group consisting of lithium bis(oxalato)borate, lithium bis(malonato) borate, lithium bis(difluoromalonato) borate, lithium (malonato oxalato) borate, lithium (difluoromalonato oxalato) borate, lithium tris(oxalato)phosphate, and lithium tris(difluoromalonato)phosphate.

12. A non-aqueous electrolytic solution for a secondary battery comprising

a. a non-aqueous solvent,

b. a solute, and

c. an aromatic phosphite compound selected from the group consisting of tris(p-fluorophenyl) phosphite), tris(perfluorophenyl) phosphite, di(p-fluorophenyl) phenyl phosphite, and di(perfluorophenyl) phenyl phosphite.

13. The non-aqueous electrolytic solution of claim 12 wherein the solute is selected from the group consisting of LiPF 6 , LiBF 4 , LiClO 4 , LiAsF 6 , LiTaF 6 , LiAlCl 4 , LiCF 3 SO 3 , Li 2 B 10 Cl 10 , Li 2 B 10 F 10 , Li 2 B 12 H x F (12-x) LiBF y (R F ) 4-y , LiPF z (R F ) 6-z , LiBF 2 [C 2 O 4 (CE 2 ) w ], LiPF 2 [C 2 O 4 (CE 2 ) w ] 2 , LiPF 4 [C 2 O 4 (CE 2 ) w ], LiN(SO 2 C m F 2m+1 )(SO 2 C n F 2n+1 ), LiC(SO 2 C k F 2k+1 )(SO 2 C m F 2m+1 )(SO 2 C n F 2n+ ), LiN(SO 2 C p F 2p SO 2 ), and LiC(SO 2 C p F 2p SO 2 )(SO 2 C q F 2q+1 ), wherein E is H, F, or Cl; wherein R F is a perfluorinated C 1 -C 20 alkyl group or perfluorinated aromatic group, wherein 1≦k, m, n, p, q, ≦10; 0≦w≦4; 0≦x≦12; 0≦y≦3; and 0≦z≦5.

14. A method of maintaining below a reading of 50 the APHA color of a non-aqueous electrolytic solution for use in a secondary battery after storage at 50° for two months, comprising contacting a non-aqueous electrolytic solution with about 0.01 to about 5 wt % of an aromatic phosphite compound selected from the group consisting of tris(p-fluorophenyl) phosphite), tris(perfluorophenyl) phosphite, di(p-fluorophenyl) phenyl phosphite, and di(perfluorophenyl) phenyl phosphite.

15. A secondary battery comprising an electrolytic solution, wherein the electrolytic solution comprises a non-aqueous solvent, a solute, and triphenyl phosphite, provided that the concentration of triphenyl phosphite in the solution does not exceed 5 wt %, wherein the triphenyl phosphite is selected from the group consisting of tris(p-fluorophenyl) phosphite), tris(perfluorophenyl) phosphite, di(p-fluorophenyl) phenyl phosphite, and di(perfluorophenyl) phenyl phosphite.

16. A non-aqueous electrolytic solution for use in a secondary battery comprising a salt and triphenyl phosphite, provided that the concentration of triphenyl phosphite in the solution does not exceed 5 wt %, wherein the triphenyl phosphite is selected from the group consisting of tris(p-fluorophenyl) phosphite), tris(perfluorophenyl) phosphite, di(p-fluorophenyl) phenyl phosphite, and di(perfluorophenyl) phenyl phosphite.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 27, 2017
From: BASF CORPORATION
To: SHENZHEN CAPCHEM TECHNOLOGY CO., LTD.
Reel/Frame 043964/0506 →
CHANGE OF NAME Recorded Oct 12, 2016
From: NOVOLYTE TECHNOLOGIES INC.
To: NOVOLYTE LEGACY TECHNOLOGIES LLC.
Reel/Frame 040324/0215 →
MERGER Recorded Oct 12, 2016
From: NOVOLYTE LEGACY TECHNOLOGIES LLC.
To: BASF CORPORATION
Reel/Frame 040336/0890 →
RELEASE OF SECURITY INTEREST Recorded May 11, 2012
From: SQUARE 1 BANK
To: SQUARE 1 BANK; NOVOLYTE TECHNOLOGIES, INC
Reel/Frame 028195/0781 →
RELEASE OF SECURITY INTEREST Recorded May 11, 2012
From: SQUARE 1 BANK
To: NOVOLYTE TECHNOLOGIES, INC
Reel/Frame 028195/0871 →
RELEASE OF SECURITY INTEREST Recorded Mar 23, 2011
From: PNC BANK, NATIONAL ASSOCIATION
To: NOVOLYTE TECHNOLOGIES INC.; NOVOLYTE TECHNOLOGIES LP
Reel/Frame 026007/0991 →