Spatially surface ion-aggregated solid polymer electrolyte with robust mechanical properties for lithium metal batteries

Solid polymer electrolytes (SPEs) show great promise for solid-state lithium batteries, but achieving mechanical robustness and fast interfacial kinetics simultaneously poses critical challenges. Herein, we introduce a spatially surface ion-aggregated SPE (SIA-SPE), featuring a LiTFSI-enriched surface layer with a dense poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) microstructure embedded in a polyethylene (PE) framework, enabled by leveraging the selective solubility of lithium salt and PVDF-HFP in fluoroethylene carbonate and dimethyl formamide co-solvents. The submicron salt-rich surface layer not only enhances lithium-ion transportation but also produces an anion-derived inorganic-rich solid electrolyte interphase with electrochemical stability and fast kinetics. In addition, the PE framework and lithium aluminum titanium phosphate nanofillers confine the crystallization of PVDF-HFP and induce a dense configuration with a β-rich phase. Consequently, the SIA-SPE delivers a remarkable tensile strength of 115 MPa and a high ambient ionic conductivity of 0.75 mS cm −1 . The SIA-SPE achieves a record-breaking performance, with a high critical current density of 10 mA cm −2 in Li||Li symmetric cells, stable cycling of 18000 cycles in Li||LiFePO 4 cells at 1.4 A g −1 , and a high capacity of 149.5 mAh g −1 over 350 cycles (8 mg cm −2 LiFePO 4 loading). Excellent performance in a high-voltage LiNi 0.8 Mn 0.1 Co 0.1 O 2 cathode over 1100 cycles and stable cycling over 1000 cycles in pouch cells further demonstrate its scalability for practical applications. • A novel surface ion-concentrated SPE with a submicron salt-rich layer is designed to produce a highly conductive, inorganic-rich SEI. • The incorporation of a PE framework and LATP nanofiller confines the crystallization of PVDF-HFP and induces a β-rich phase with a dense morphology and robust mechanical properties. • A record high rate capacity of over 20 C and long-term cycling performance for 18000 cycles are achieved.

Authors

Institutions

Publication Details

Journal
eScience
Published
2025-08-26
DOI
https://doi.org/10.1016/j.esci.2025.100462
Citations
8
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
5.84

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Spatially surface ion-aggregated solid polymer electrolyte with robust mechanical properties for lithium metal batteries

Bo Liu, Minfeng Chen, Guiming Zhong, Zhangquan Peng et al.
8 citations
eScience
Advanced Battery Materials and Technologies
5.84
article

Spatially surface ion-aggregated solid polymer electrolyte with robust mechanical properties for lithium metal batteries

Bo Liu, Minfeng Chen, Guiming Zhong, Zhangquan Peng, Jizhang Chen, Qing-Qing Zhou, Qiu Fang, Bin Wang, Xuefeng Wang, Hongli Chen, Xiang Han, Junjie Lu, Chuyang Li, Bifu Sheng
article en
8 citations

Abstract

Solid polymer electrolytes (SPEs) show great promise for solid-state lithium batteries, but achieving mechanical robustness and fast interfacial kinetics simultaneously poses critical challenges. Herein, we introduce a spatially surface ion-aggregated SPE (SIA-SPE), featuring a LiTFSI-enriched surface layer with a dense poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) microstructure embedded in a polyethylene (PE) framework, enabled by leveraging the selective solubility of lithium salt and PVDF-HFP in fluoroethylene carbonate and dimethyl formamide co-solvents. The submicron salt-rich surface layer not only enhances lithium-ion transportation but also produces an anion-derived inorganic-rich solid electrolyte interphase with electrochemical stability and fast kinetics. In addition, the PE framework and lithium aluminum titanium phosphate nanofillers confine the crystallization of PVDF-HFP and induce a dense configuration with a β-rich phase. Consequently, the SIA-SPE delivers a remarkable tensile strength of 115 MPa and a high ambient ionic conductivity of 0.75 mS cm −1 . The SIA-SPE achieves a record-breaking performance, with a high critical current density of 10 mA cm −2 in Li||Li symmetric cells, stable cycling of 18000 cycles in Li||LiFePO 4 cells at 1.4 A g −1 , and a high capacity of 149.5 mAh g −1 over 350 cycles (8 mg cm −2 LiFePO 4 loading). Excellent performance in a high-voltage LiNi 0.8 Mn 0.1 Co 0.1 O 2 cathode over 1100 cycles and stable cycling over 1000 cycles in pouch cells further demonstrate its scalability for practical applications. • A novel surface ion-concentrated SPE with a submicron salt-rich layer is designed to produce a highly conductive, inorganic-rich SEI. • The incorporation of a PE framework and LATP nanofiller confines the crystallization of PVDF-HFP and induces a β-rich phase with a dense morphology and robust mechanical properties. • A record high rate capacity of over 20 C and long-term cycling performance for 18000 cycles are achieved.

eScienceVol. 6(3)
East China University of Science and Technology (CN), Jinggangshan University (CN), Nanjing Forestry University (CN), Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), State Key Laboratory of Chemical Engineering (CN), Institute of Physics (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences, Jiangsu Association for Science and Technology
Affordable and clean energy
Openalex Percentile: Top 4%
Advanced Battery Materials and Technologies
5.84
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.