IP Library › Granted Patent US 12,573,655
Granted Patent B2
US 12,573,655 · App. 17/605,952 · Granted Mar 10, 2026

Lithium-sulfur secondary battery

Inventors: Habin Chung (Daejeon, KR); Kwonnam Sohn (Daejeon, KR); Changhun Park (Daejeon, KR); Minsu Kim (Daejeon, KR)
Assignee: LG ENERGY SOLUTION, LTD.
H01M10/056H01M10/0568H01M10/0569H01M2004/021H01M10/0525H01M10/14H01M2300/004
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Quick Facts
Patent No.
US 12,573,655
App. No.
17/605,952
Granted
Mar 10, 2026
Kind
B2
Abstract

Disclosed is a lithium-sulfur secondary battery including a positive electrode, a negative electrode, a separator, and an electrolyte solution, wherein the electrolyte solution contains a lithium salt and a solvent, the solvent includes a nitrile-based solvent, a fluorinated ether-based solvent, and a disulfide-based solvent in a specific volume ratio, and thus for the positive electrode that satisfies the specific conditions of high loading and low porosity, the initial discharging capacity and average discharging voltage of the lithium-sulfur secondary battery containing the electrolyte solution may be improved.

Claims (37)

1 . A lithium-sulfur secondary battery comprising:

a positive electrode;

a negative electrode;

a separator; and

an electrolyte solution comprising a lithium salt and a solvent,

wherein a concentration of the lithium salt is 1.5 M (mol/L) to 2.5 M (mol/L),

wherein the solvent comprises a nitrile-based solvent, a fluorinated ether-based solvent, and a disulfide-based solvent,

wherein the nitrile-based solvent is at least one selected from the group consisting of acetonitrile, propionitrile, butyronitrile, valeronitrile, caprylonitrile, heptanenitrile, cyclopentane carbonitrile, cyclohexane carbonitrile, 2-fluorobenzonitrile, 4-fluorobenzonitrile, difluorobenzonitrile, trifluorobenzonitrile, phenylacetonitrile, 2-fluorophenylacetonitrile, and 4-fluorophenylacetonitrile,

wherein the fluorinated ether-based solvent is at least one selected from the group consisting of 2,2,2-trifluoroethylmethylether(CF 3 CH 2 OCH 3 ), 2,2,2trifluoroethyldifluoromethylether(CF 3 CH 2 OCHF 2 ), 2,2,3,3,3-pentafluoropropylmethylether(CF 3 CF 2 CH 2 OCH 3 ), 2,2,3,3,3-pentafluoropropyldifluoromethylether(CF 3 CF 2 CH 2 OCHF 2 ), 2,2,3,3,3-pentafluoropropyl-1,1,2,2-tetrafluoroethylether(CF 3 CF 2 CH 2 OCF 2 CF 2 H), 1,1,2,2-tetrafluoroethylmethylether(HCF 2 CF 2 OCH 3 ), 1,1,2,2-tetrafluoroethylethylether(HCF 2 CF 2 OCH 2 CH 3 ), 1,1,2,2-tetrafluoroethylpropylether(HCF 2 CF 2 OC 3 H 7 ), 1,1,2,2-tetrafluoroethylbutylether(HCF 2 CF 2 OC 4 H 9 ), 2,2,3,3-tetrafluoroethyldifluoromethylether(H(CF 2 ) 2 CH 2 O(CF 2 )H), 1,1,2,2-tetrafluoroethylisobutylether(HCF 2 CF 2 OCH 2 CH(CH 3 ) 2 ), 1,1,2,2-tetrafluoroethylisopentylether(HCF 2 CF 2 OCH 2 C(CH 3 ) 3 ), 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethylether(HCF 2 CF 2 OCH 2 CF 3 ), 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropylether(HCF 2 CF 2 OCH 2 CF 2 CF 2 H), hexafluoroisopropylmethylether((CF 3 ) 2 CHOCH 3 ), 1,1,3,3,3-pentafluoro-2-trifluoromethylpropylmethylether((CF 3 ) 2 CHCF 2 OCH 3 ), 1,1,2,3,3,3-hexafluoropropylmethylether(CF 3 CHFCF 2 OCH 3 ), 1,1,2,3,3,3-hexafluoropropylethylether(CF 3 CHFCF 2 OCH 2 CH 3 ), and 2,2,3,4,4,4-hexafluorobutyldifluoromethylether(CF 3 CHFCF 2 CH 2 OCHF 2 ),

wherein the disulfide-based solvent is dimethyl disulfide,

wherein the nitrile-based solvent is present in the solvent in an amount of 25 to 35 vol. % based on the total volume of the solvent,

wherein the fluorinated ether-based solvent is present in the solvent in an amount of 30 to 50 vol. % of the total volume of the solvent,

wherein the disulfide-based solvent is present in the solvent in an amount of 20 to 35 vol. % based on the total volume of the solvent,

wherein the positive electrode has an SC factor value of 0.45 or more, expressed by Equation 1 below [Equation 1]

SC

⁢

⁢

factor

=

α

×

L

p

[

Equation

⁢

⁢

1

]

wherein

P is the porosity (%) of a positive electrode active material layer in the positive electrode,

L is the mass of sulfur per unit area (mg/cm 2 ) of the positive electrode active material layer in the positive electrode, and

α is 10.

2 . The lithium-sulfur secondary battery according to claim 1 , wherein the lithium salt is at least one selected from the group consisting of LiCl, LiBr, LiI, LiClO 4 , LiBF 4 , LiB 10 Cl 10 , LiB(Ph) 4 , LiC 4 BO 8 , LiPF 6 , LiCF 3 SO 3 , LiCF 3 CO 2 , LiAsF 6 , LiSbF 6 , LiAlCl 4 , LiSO 3 CH 3 , LiSO 3 CF 3 , LiSCN, LiC(CF 3 SO 2 ) 3 , LiN (CF 3 SO 2 ) 2 , LiN(C 2 F 5 SO 2 ) 2 , LiN(SO 2 F) 2 , lithium chloroborane, lithium lower aliphatic carboxylate, and lithium imide.

3 . The lithium-sulfur secondary battery according to claim 1 , wherein a volume ratio of the fluorinated ether-based solvent and the disulfide-based solvent is 1:0.75 to 1:1.

4 . The lithium-sulfur secondary battery according to claim 1 , wherein the mass of sulfur per unit area (mg/cm 2 ) of the positive electrode active material layer in the positive electrode is 2.5 mg/cm 2 to 5.0 mg/cm 2 .

5 . The lithium-sulfur secondary battery according to claim 1 , wherein the porosity (%) of the positive electrode active material layer in the positive electrode is 50 to 70%.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 25, 2021
From: CHUNG, HABIN; SOHN, KWONNAM; PARK, CHANGHUN; KIM, MINSU
To: LG ENERGY SOLUTION, LTD.
Reel/Frame 058395/0419 →
Priority Claims (1)
KR 10-2019-0134367 · Oct 28, 2019 · national
Continuity (1)
Related Publication 20220231323A1 · Jul 21, 2022
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