journal article·2026-07-09

Asymmetric Ultrathin Salt-Rich Composite Polymer Electrolyte Formed by Spin Coating for High-Performance Lithium Metal Batteries

Shuaitian Jia, Linxin Yang, Yanpei Wang, Lifeng Zhang, Langli Luo

Publisher page

Abstract

Solid-state lithium metal batteries (SSLMBs) are being intensively explored as next-generation energy storage solutions, combining high energy density with enhanced safety. However, conventional composite polymer electrolytes face critical challenges including low room-temperature ionic conductivity, limited lithium ion (Li + ) transference numbers, and mechanically incompatible interfaces. Herein, we design a spin-coated asymmetric high-salt polymer electrolyte where a polyvinylidene fluoride (PVDF) framework spans the entire membrane while a sulfolane-containing polyethylene oxide (PEO)/lithium bis(trifluoromethanesulfonyl)imide (LiTFSI)-rich cathode-side layer establishes a high-dielectric microenvironment. This converts ion aggregates into free Li + coordinated with ether oxygens, endowing the cathode side with low interfacial impedance and a robust solid electrolyte interphase (CEI). Meanwhile, the anode side maintains high modulus and homogenized Li + flux to suppress dendrite growth. Dispersed lithium lanthanum titanate (LLTO) fillers further construct an inorganic percolated pathway for Li + transport. This spin-coated asymmetric electrolyte achieves an optimized Li + transference number of 0.78. Full cells paired with lithium iron phosphate (LFP) and Li anodes deliver 82.5% capacity retention after 500 cycles accompanied by nearly 100% Coulombic efficiency and excellent rate-capability recovery. Our results highlight the potential of this asymmetric high-salt polymer electrolyte platform for developing thin, high-energy density SSLMBs.
Source: openalex_inverted_index · Quality: baseline

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

Institute of Molecular Plus, Department of Chemistry

Tianjin University

Haihe Laboratory of Sustainable Chemical Transformations

Funding

National Natural Science Foundation of China (NSFC)

References (28)

Show source-provided references
1. 10.1038/s41560-023-01426-110.1038/s41560-023-01426-1 ↗
2. 10.1039/D0EE02525A10.1039/D0EE02525A ↗
3. 10.1039/D5EE01767J10.1039/D5EE01767J ↗
4. 10.1016/j.mser.2018.10.00410.1016/j.mser.2018.10.004 ↗
5. 10.1021/acsnano.5c0710510.1021/acsnano.5c07105 ↗
6. 10.1007/s40820-023-01051-310.1007/s40820-023-01051-3 ↗
7. 10.1002/adma.20251037610.1002/adma.202510376 ↗
8. 10.1016/j.ensm.2023.10282110.1016/j.ensm.2023.102821 ↗
9. 10.1016/j.scriptamat.2025.11691010.1016/j.scriptamat.2025.116910 ↗
10. 10.1016/j.jechem.2025.02.00910.1016/j.jechem.2025.02.009 ↗
11. 10.1002/aenm.20220403610.1002/aenm.202204036 ↗
12. 10.1039/D4CS00214H10.1039/D4CS00214H ↗
13. 10.1002/sus2.9310.1002/sus2.93 ↗
14. 10.1016/j.enchem.2021.10005810.1016/j.enchem.2021.100058 ↗
15. 10.1007/s40820-024-01389-210.1007/s40820-024-01389-2 ↗
16. 10.1002/aenm.20220364010.1002/aenm.202203640 ↗
17. 10.1038/s41563-022-01319-w10.1038/s41563-022-01319-w ↗
18. 10.1016/j.cej.2024.15416310.1016/j.cej.2024.154163 ↗
19. 10.1016/j.est.2025.11810910.1016/j.est.2025.118109 ↗
20. 10.1002/adfm.20210304910.1002/adfm.202103049 ↗
21. 10.1039/D4TA03543G10.1039/D4TA03543G ↗
22. 10.1016/j.ensm.2025.10451310.1016/j.ensm.2025.104513 ↗
23. 10.1002/aenm.20210177510.1002/aenm.202101775 ↗
24. 10.1038/s41467-022-29103-z10.1038/s41467-022-29103-z ↗
25. 10.1021/jacs.0c1253810.1021/jacs.0c12538 ↗
26. 10.1016/j.nanoen.2024.11058210.1016/j.nanoen.2024.110582 ↗
27. 10.1002/adfm.20220982810.1002/adfm.202209828 ↗
28. 10.1038/s41467-023-43467-w10.1038/s41467-023-43467-w ↗