IP Library Granted Patent US 12,542,301
Granted Patent B2
US 12,542,301 · App. 18/062,583 · Granted Feb 3, 2026

Supramolecular ionic liquid, solid-state electrolyte membrane, solid-state lithium metal battery, and apparatus

Inventors: Qian Li (Ningde, CN); Chengyong Liu (Ningde, CN); Yongsheng Guo (Ningde, CN); Jiawei Fu (Ningde, CN); Bobing Hu (Ningde, CN); Meng Cheng (Ningde, CN); Ang Fu (Ningde, CN)
Assignee: CONTEMPORARY AMPEREX TECHNOLOGY (HONG KONG) LIMITED
H01M10/0565C07C309/07H01M10/052C07C2603/42H01M2300/0045H01M2300/0082
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Quick Facts
Patent No.
US 12,542,301
App. No.
18/062,583
Granted
Feb 3, 2026
Kind
B2
Abstract

A supramolecular ionic liquid, a solid-state electrolyte membrane, a solid-state lithium metal battery, and an apparatus are provided. The supramolecular ionic liquid of this disclosure has a benzophenanthrene structure represented by formula (I), where R 1 is selected from ether groups, polyether groups, halogenated ether groups, or halogenated polyether groups having 1 to 16 carbon atoms; and R 2 is selected from ether groups or polyether groups having 1 to 16 carbon atoms. The supramolecular ionic liquid of this disclosure has an ionic conductivity as high as 10 −3 S/cm at room temperature. A solid-state electrolyte membrane made therefrom also has an ionic conductivity as high as 10 −3 S/cm at room temperature. This is close to performance of a liquid electrolyte, proposing a solution to the problem of low ionic conductivity in existing solid-state electrolytes.

Claims (46)

1 . A solid-state electrolyte membrane comprising a supramolecular ionic liquid, wherein the supramolecular ionic liquid comprises a benzophenanthrene structure represented by formula (I):

wherein

R 1 is selected from ether groups, polyether groups, halogenated ether groups, or halogenated polyether groups having 1 to 16 carbon atoms; and

R 2 is selected from ether groups or polyether groups having 1 to 16 carbon atoms.

2 . The solid-state electrolyte membrane according to claim 1 , wherein R 1 is selected from structures represented by formula (II):

wherein

m1 is selected from 1-6,

n1 is selected from 1-5,

p1 is selected from 0-4, and

Y is selected from H, F, Cl, or Br.

3 . The solid-state electrolyte membrane according to claim 2 , wherein the formula (II) meets at least one of the following conditions:

(1) m1 is selected from 2-3;

(2) n1 is selected from 2-3;

(3) p1 is selected from 1-2; and

(4) Y is selected from H or F.

4 . The solid-state electrolyte membrane according to claim 1 , wherein R 2 is selected from structures represented by formula (III):

wherein

when n2 is not 0, m2 is selected from 1-6, n2 is selected from 1-5, and p2 is selected from 0-4; and

when n2 is 0, p2 is selected from 1-16, and optionally, p2 is selected from 4-10.

5 . The solid-state electrolyte membrane according to claim 4 , wherein

when n2 is not 0, the formula (III) meets at least one of the following conditions:

(1) m2 is selected from 2-3;

(2) n2 is selected from 2-3; and

(3) p2 is selected from 1-2.

6 . The solid-state electrolyte membrane according to claim 1 , wherein R 1 and R 2 in the formula (I) are selected from one of I-1 to I-22:

7 . The solid-state electrolyte membrane according to claim 1 , wherein the supramolecular ionic liquid is a cylindrical structure formed by a number of the benzophenanthrene structures through π-π stacking and self assembly.

8 . The solid-state electrolyte membrane according to claim 1 , wherein a q value of small-angle X-ray scattering peak of the supramolecular ionic liquid is 15.5 nm −1 to 18.8 nm −1 ; optionally, the q value is 16.0 nm −1 to 18.5 nm −1 , and further optionally, the q value is 16.3 nm −1 to 18.2 nm −1 .

9 . The solid-state electrolyte membrane according to claim 1 , wherein ionic conductivity of the supramolecular ionic liquid at 25° C. is 2*10 −5 S/cm to 7*10 −3 S/cm; optionally, the ionic conductivity is 1.5*10 −3 S/cm to 6.5*10 −3 S/cm.

10 . The solid-state electrolyte membrane according to claim 1 , wherein the solid-state electrolyte membrane further comprises a polymer matrix, and the polymer matrix meets at least one of the following conditions:

(1) the polymer matrix comprises a viscoelastic polymer, and a relative molecular mass of the polymer matrix is 1,000-2,000,000;

(2) crystallinity of the polymer matrix is 1%-40%, optionally, 5%-25%;

(3) the polymer matrix comprises a first polymer and a second polymer, wherein a relative molecular mass of the first polymer is 400,000-800,000, and a relative molecular mass of the second polymer is 1,000-10,000,

optionally, a mass ratio of the first polymer and the second polymer is 10:1-5:1; and

(4) the polymer matrix is selected from one or more of polyethylene oxide, polyethylene terephthalate, polyimide, polyvinylidene fluoride, polymethyl methacrylate, polyacrylonitrile, polypropylene carbonate, polyvinyl chloride, or polyvinylidene fluoride-(2-acrylamido-2-methylpropane sulfonic acid)-trimethylolpropane triacrylate-hyperbranched polyacrylate-methyl methacrylate-copolymer, and optionally, the polymer matrix is selected from one or more of polyethylene oxide, polyvinylidene fluoride, or polymethyl methacrylate.

11 . The solid-state electrolyte membrane according to claim 1 , wherein the solid-state electrolyte membrane further comprises a lithium salt, and the lithium salt is selected from one or more of LiPF 6 , LiBF 4 , LiClO 4 , LiAsF 6 , LiCF 3 SO 3 , LiFSI, or LiTFSI; and optionally, the lithium salt is LiTFSI.

12 . A solid-state lithium metal battery, comprising the solid-state electrolyte membrane according to claim 1 .

13 . An apparatus, comprising the solid-state lithium metal battery according to claim 12 , wherein the solid-state lithium metal battery is capable of serving as a power source of the apparatus or as an energy storage unit of the apparatus.

14 . A method for preparing a solid-state electrolyte membrane, the method comprising:

providing a polymer matrix, a lithium salt, and a supramolecular ionic liquid; and

mixing, hot pressing, and vacuum annealing the polymer matrix, the lithium salt, and the supramolecular ionic liquid to obtain the solid-state electrolyte membrane,

wherein the supramolecular ionic liquid comprises a benzophenanthrene structure represented by formula (I):

wherein

R 1 is selected from ether groups, polyether groups, halogenated ether groups, or halogenated polyether groups having 1 to 16 carbon atoms; and

R 2 is selected from ether groups or polyether groups having 1 to 16 carbon atoms.

15 . The method according to claim 14 , wherein

a mass ratio of the polymer matrix, the lithium salt, and the supramolecular ionic liquid is 100:(5-40):(10-80).

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 6, 2024
From: CONTEMPORARY AMPEREX TECHNOLOGY CO., LIMITED
To: CONTEMPORARY AMPEREX TECHNOLOGY (HONG KONG) LIMITED
Reel/Frame 068338/0402 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 7, 2022
From: LI, QIAN; LIU, CHENGYONG; GUO, YONGSHENG; FU, JIAWEI; HU, BOBING; CHENG, MENG; FU, ANG
To: CONTEMPORARY AMPEREX TECHNOLOGY CO., LIMITED
Reel/Frame 062078/0744 →
Continuity (2)
Continuation PCTCN2020105917 · Jul 30, 2020
Related Publication 20230198015A1 · Jun 22, 2023
References Cited (20)
US 6464904B1 · Hirose et al. · 2002 [cited by applicant]
US 6692658B2 · Nakamura · 2004 [cited by examiner]
US 20020017632A1 · Nakamura et al. · 2002 [cited by applicant]
US 20180261886A1 · Picard et al. · 2018 [cited by applicant]
US 20190157715A1 · Makino et al. · 2019 [cited by applicant]
US 20210020986A1 · Shen · 2021 [cited by examiner]
CN 106654364A · 2017 [cited by applicant]
CN 108878966A · 2018 [cited by applicant]
CN 110098378A · 2019 [cited by applicant]
CN 111193064A · 2020 [cited by applicant]
CN 111244537A · 2020 [cited by applicant]
EP 3109924A1 · 2016 [cited by applicant]
JP 2004115477A · 2004 [cited by applicant]
WO 2019170694A1 · 2019 [cited by applicant]
WO 2020143259A1 · 2020 [cited by applicant]
Machine translation of JP 2004-115477 A (Year: 2004). [cited by examiner]
First Office Action received in the counterpart Chinese Application 202080095432.9, mailed on May 18, 2024. [cited by applicant]
Extended European search report received in the counterpart European Application 20947397.4, mailed on Jul. 2, 2024. [cited by applicant]
International Search Report received in International Application PCT/CN2020/105917, mailed Mar. 30, 2021. [cited by applicant]
Written Opinion received in International Application PCT/CN2020/105917, mailed Mar. 30, 2021. [cited by applicant]