journal article·2026-02Open access

Mortise‐Tenon Joint Inspired Weakly Solvated Gel Electrolyte Based on Halogen Bonds for High‐Voltage Lithium Metal Batteries

Shuohan Liu, Wensheng Tian, Hui Pan, Shunwei Chen, Xiujun Han, Hengdao Quan, Shenmin Zhu

Advanced Science· Volume 13· Issue 7

Abstract

Abstract In situ gel polymer electrolytes (GPEs) offer a promising approach to improve safety and cycling stability in lithium metal batteries (LMBs), yet often suffer from poor electrode compatibility, especially at high temperatures. This work reports a “mortise‐tenon joint” inspired non‐covalent interaction — “π‐hole” based halogen bond, that enables solvation structure regulation beyond traditional van der Waals force or hydrogen bond. The electrophilic π‐hole on the polymer skeleton engages in halogen bonding with solvents, thereby weakening their coordination with Li + to form a weakly solvated structure. Moreover, the fluorine‐rich skeleton participates in the formation of the electrode‐electrolyte interphases, achieving good anode compatibility and high‐voltage stability simultaneously. The resulting electrolyte exhibits high ionic conductivity (0.30 mS cm −1 ) and a Li + transference number of 0.84. Li symmetric cells stably cycle over 1000 h. The Li/LiNi 0.8 Co 0.1 Mn 0.1 O 2 (NCM811) cell delivers discharge specific capacities of 161.0 mAh g −1 after 500 cycles at 1C. Especially, the cell can work stably for 100 cycles at 80 °C (1C, 156.0 mAh g −1 ). Furthermore, the pouch cell achieves an energy density of 462.2 Wh kg −1 . This study demonstrates that the concept of a weakly solvated gel electrolyte based on halogen bonds provides a new approach to achieving high‐energy‐density LMBs.
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Research context

OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Thermal Expansion and Ionic Conductivity

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Metal Matrix Composites School of Materials Science and Engineering Shanghai Jiao Tong University Shanghai 200240 China

State Key Laboratory of Space Power‐Sources Shanghai Institute of Space Power‐Sources Shanghai 200245 China

School of Materials Science and Engineering Qilu University of Technology (Shandong Academy of Sciences) Jinan Shandong 250353 China

School of Materials and Chemistry University of Shanghai for Science and Technology Shanghai 200093 China

Funding

National Natural Science Foundation of China

References (53)

Show source-provided references
1. 10.1038/s41467-023-36853-x10.1038/s41467-023-36853-x ↗
2. 10.1002/smll.20230638110.1002/smll.202306381 ↗
3. 10.1002/adfm.20231080110.1002/adfm.202310801 ↗
4. 10.1002/aesr.20220002210.1002/aesr.202200022 ↗
5. 10.1002/adma.20251037610.1002/adma.202510376 ↗
6. 10.1002/ange.20251345010.1002/ange.202513450 ↗
7. 10.1002/smll.20230755310.1002/smll.202307553 ↗
8. 10.1021/acsami.2c0910310.1021/acsami.2c09103 ↗
9. 10.1016/j.ensm.2024.10368310.1016/j.ensm.2024.103683 ↗
10. 10.1038/s41586-021-03885-610.1038/s41586-021-03885-6 ↗
11. 10.1039/D5EE02373D10.1039/D5EE02373D ↗
12. 10.1016/j.jpowsour.2024.23418310.1016/j.jpowsour.2024.234183 ↗
13. 10.1016/j.ensm.2022.12.02010.1016/j.ensm.2022.12.020 ↗
14. 10.1016/j.ensm.2022.10.01910.1016/j.ensm.2022.10.019 ↗
15. 10.1002/cssc.20230067110.1002/cssc.202300671 ↗
16. 10.1021/acsenergylett.1c0242510.1021/acsenergylett.1c02425 ↗
17. 10.1021/acsenergylett.2c0140810.1021/acsenergylett.2c01408 ↗
18. 10.1002/anie.20242279110.1002/anie.202422791 ↗
19. 10.1002/1521-3773(20020104)41:1<48::AID-ANIE48>3.0.CO;2-U10.1002/1521-3773(20020104)41:1<48::AID-ANIE48>3.0.CO;2-U ↗
20. 10.1002/aenm.20220354710.1002/aenm.202203547 ↗
21. 10.1021/acs.chemrev.5b0052710.1021/acs.chemrev.5b00527 ↗
22. 10.1002/cphc.20190096810.1002/cphc.201900968 ↗
23. 10.1021/jacs.4c0950410.1021/jacs.4c09504 ↗
24. 10.1021/jp309102c10.1021/jp309102c ↗
25. 10.1016/j.cej.2024.15181210.1016/j.cej.2024.151812 ↗
26. 10.1002/adma.20250207610.1002/adma.202502076 ↗
27. 10.1002/adfm.20231552710.1002/adfm.202315527 ↗
28. 10.1038/s41467-025-57856-w10.1038/s41467-025-57856-w ↗
29. 10.1021/acsenergylett.8b0248310.1021/acsenergylett.8b02483 ↗
30. 10.1021/acsami.2c0151310.1021/acsami.2c01513 ↗
31. 10.1016/j.nanoen.2023.10905410.1016/j.nanoen.2023.109054 ↗
32. 10.1002/adfm.20190104710.1002/adfm.201901047 ↗
33. 10.1002/anie.20242522110.1002/anie.202425221 ↗
34. 10.1002/adfm.20200992510.1002/adfm.202009925 ↗
35. 10.1021/acsami.0c0235410.1021/acsami.0c02354 ↗
36. 10.1002/advs.20200330110.1002/advs.202003301 ↗
37. 10.1002/smll.20250555210.1002/smll.202505552 ↗
38. 10.1016/j.ensm.2023.02.02710.1016/j.ensm.2023.02.027 ↗
39. 10.1038/s41467-022-35636-010.1038/s41467-022-35636-0 ↗
40. 10.1002/adma.20230722010.1002/adma.202307220 ↗
41. 10.1039/D4EE04011B10.1039/D4EE04011B ↗
42. 10.1021/acsami.5c0851710.1021/acsami.5c08517 ↗
43. 10.1002/ange.20221568010.1002/ange.202215680 ↗
44. 10.1021/acsami.2c0910310.1021/acsami.2c09103 ↗
45. 10.1039/D3EE00558E10.1039/D3EE00558E ↗
46. 10.1016/j.ensm.2022.05.05110.1016/j.ensm.2022.05.051 ↗
47. 10.1002/aenm.20220249310.1002/aenm.202202493 ↗
48. 10.1016/j.nanoen.2020.10528210.1016/j.nanoen.2020.105282 ↗
49. 10.1021/acsnano.4c0995310.1021/acsnano.4c09953 ↗
50. 10.1021/acsnano.4c0987810.1021/acsnano.4c09878 ↗
51. 10.1002/ange.20231560810.1002/ange.202315608 ↗
52. 10.1002/adfm.20230686810.1002/adfm.202306868 ↗
53. 10.1002/anie.20240079710.1002/anie.202400797 ↗