journal article·2026-07Open access

Tailoring the Work Function of Oxyhalide Solid Electrolytes via Sulfur Doping to Boost High‐Performance All‐Solid‐State Lithium Batteries

Rongzeng Jin, Shaowei Li, Yile Ding, Jia‐ao Wang, Zihao Zhang, Ke Yue, Chenglong Li, Yutong Wang, Yiqun Wu, Chengpu Diao, Mengjie Wu, Yao Wang, Peng Shi, Shihui Zou, Yujing Liu, Jianwei Nai, Jianmin Luo, Xinyong Tao, Huadong Yuan

Small· Volume 22· Issue 40

Abstract

ABSTRACT Achieving high ionic conductivity alongside interfacial stability is essential yet challenging for solid‐state electrolytes. Here, we report a sulfur‐doped oxohalide solid‐state electrolyte, LiTaO 0.5 S 0.5 Cl 4 , synthesized via a facile high‐energy ball milling method. Confirmed by the experimental and theoretical simulation results, sulfur incorporation significantly elevates the work function and ionization energy to 4.54 and 8.0 eV, respectively, reducing electron availability for interfacial charge transfer and enhancing oxidative stability against high‐voltage cathodes. In addition, the coexistence of S 2− and O 2− promotes in‐situ formation of a Ta 2 O/TaS 2 composite protective layer, featuring high electronic insulation and low Li + migration barrier. Consequently, the all‐solid‐state Li battery delivers a high‐capacity retention of 75.5% after 500 cycles at 0.5 C using LiNi 0.8 Co 0.1 Mn 0.1 O 2 cathodes. This work demonstrates that anion doping is an effective strategy for concurrently improving ionic conductivity and cathode interfacial stability.
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Research context

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

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Affiliations

College of Materials Science and Engineering Zhejiang University of Technology Hangzhou Zhejiang China

Science and Education Integration College of Energy and Carbon Neutralization Zhejiang University of Technology Hangzhou China

State Key Laboratory of Green Chemical Synthesis and Conversion Zhejiang University of Technology Hangzhou China

Funding

National Natural Science Foundation of China · Natural Science Foundation of Zhejiang Province

References (38)

Show source-provided references
1. 10.1038/nenergy.2016.4210.1038/nenergy.2016.42 ↗
2. 10.1002/adma.20220662510.1002/adma.202206625 ↗
3. 10.1021/acs.chemrev.4c0101210.1021/acs.chemrev.4c01012 ↗
4. 10.1038/s41578‐025‐00817‐y10.1038/s41578‐025‐00817‐y ↗
5. 10.1021/acs.chemrev.4c0089410.1021/acs.chemrev.4c00894 ↗
6. 10.1038/s41563‐023‐01535‐y10.1038/s41563‐023‐01535‐y ↗
7. 10.1038/s41563‐025‐02374‐910.1038/s41563‐025‐02374‐9 ↗
8. 10.1002/aenm.20230342210.1002/aenm.202303422 ↗
9. 10.1021/jacs.5c1028310.1021/jacs.5c10283 ↗
10. 10.1007/s41918‐023‐00179‐510.1007/s41918‐023‐00179‐5 ↗
11. 10.1021/acsenergylett.0c0169010.1021/acsenergylett.0c01690 ↗
12. 10.1016/j.jpowsour.2025.23642410.1016/j.jpowsour.2025.236424 ↗
13. 10.1002/adma.20251325510.1002/adma.202513255 ↗
14. 10.1002/aenm.20250406710.1002/aenm.202504067 ↗
15. 10.1021/jacs.5c1721310.1021/jacs.5c17213 ↗
16. 10.1039/D5EE02411K10.1039/D5EE02411K ↗
17. 10.1002/anie.20221758110.1002/anie.202217581 ↗
18. 10.1039/D4EE00750F10.1039/D4EE00750F ↗
19. 10.1038/s41467‐025‐65702‐210.1038/s41467‐025‐65702‐2 ↗
20. 10.1002/adfm.20251665710.1002/adfm.202516657 ↗
21. 10.1002/adma.20250310710.1002/adma.202503107 ↗
22. 10.1016/j.jechem.2025.07.04210.1016/j.jechem.2025.07.042 ↗
23. 10.1002/adma.20241119710.1002/adma.202411197 ↗
24. 10.1002/aenm.20250522310.1002/aenm.202505223 ↗
25. 10.1002/adma.20251459210.1002/adma.202514592 ↗
26. 10.1002/aenm.20250242510.1002/aenm.202502425 ↗
27. 10.1002/adfm.20241000810.1002/adfm.202410008 ↗
28. 10.1038/s41560‐025‐01853‐210.1038/s41560‐025‐01853‐2 ↗
29. 10.1021/jacs.5c1148010.1021/jacs.5c11480 ↗
30. 10.1002/aenm.20180393510.1002/aenm.201803935 ↗
31. 10.1002/anie.20250408410.1002/anie.202504084 ↗
32. 10.1002/aenm.20220409810.1002/aenm.202204098 ↗
33. 10.1002/aenm.20230238310.1002/aenm.202302383 ↗
34. 10.1016/j.ensm.2025.10451210.1016/j.ensm.2025.104512 ↗
35. 10.1002/adma.20250206710.1002/adma.202502067 ↗
36. 10.1038/s41467-024-48585-710.1038/s41467-024-48585-7 ↗
37. 10.1126/science.adt967810.1126/science.adt9678 ↗
38. 10.1016/j.est.2023.10679010.1016/j.est.2023.106790 ↗