A Solvent-Induced Solid Polymer Electrolyte with Controllable Polymerization for Low-Temperature Lithium Metal Batteries

Solid-state electrolytes based on in situ ring-opening polymerization of 1,3-dioxolane (DOL) have attracted widespread attention in Li metal batteries because of their high interface compatibility. However, its conventional cationic polymerization mechanism frequently results in the formation of long polymer chains during in situ polymerization, thereby impeding Li<sup>+</sup> transport. Here, we regulate the ring opening polymerization of DOL by introducing <i>N</i>,<i>N</i>-dimethyltrifluoroacetamide (FDMA), thus avoiding the formation of long polymer chains. Meanwhile, FDMA can derive a stable SEI rich in LiF during electrochemical cycling, improving interface stability and suppressing dendritic Li growth. Therefore, the full battery with LiFePO<sub>4</sub> as the cathode can achieve a high capacity retention rate of 83.9% after 400 cycles at a rate of 5.0 C. At -20 °C, the Li∥LiFePO<sub>4</sub> full battery can provide a high capacity of 137 mAh g<sup>-1</sup>. The solvent-induced strategy provides a promising new avenue for designing a solid electrolyte with high temperature resistance.

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Institutions

Publication Details

Journal
Nano Letters
Published
2025-03-25
DOI
https://doi.org/10.1021/acs.nanolett.4c06471
Citations
16
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
11.69

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article

A Solvent-Induced Solid Polymer Electrolyte with Controllable Polymerization for Low-Temperature Lithium Metal Batteries

Qian Wang, Lifeng Hou, Shuai Liu, Hao Huang et al.
16 citations
Nano Letters
Advanced Battery Materials and Technologies
11.69
article

A Solvent-Induced Solid Polymer Electrolyte with Controllable Polymerization for Low-Temperature Lithium Metal Batteries

Qian Wang, Lifeng Hou, Shuai Liu, Hao Huang, Bai Xiang, Xinyue Chang, Bing Wu, Jiahui Zhang, Shi Wang, Zhong Jin, Yinghui Wei
article en
16 citations

Abstract

Solid-state electrolytes based on in situ ring-opening polymerization of 1,3-dioxolane (DOL) have attracted widespread attention in Li metal batteries because of their high interface compatibility. However, its conventional cationic polymerization mechanism frequently results in the formation of long polymer chains during in situ polymerization, thereby impeding Li<sup>+</sup> transport. Here, we regulate the ring opening polymerization of DOL by introducing <i>N</i>,<i>N</i>-dimethyltrifluoroacetamide (FDMA), thus avoiding the formation of long polymer chains. Meanwhile, FDMA can derive a stable SEI rich in LiF during electrochemical cycling, improving interface stability and suppressing dendritic Li growth. Therefore, the full battery with LiFePO<sub>4</sub> as the cathode can achieve a high capacity retention rate of 83.9% after 400 cycles at a rate of 5.0 C. At -20 °C, the Li∥LiFePO<sub>4</sub> full battery can provide a high capacity of 137 mAh g<sup>-1</sup>. The solvent-induced strategy provides a promising new avenue for designing a solid electrolyte with high temperature resistance.

Nano LettersVol. 25(13)
Nanjing University of Posts and Telecommunications (CN), China Coal Research Institute (China) (CN), Nanjing University (CN), Taiyuan University of Technology (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Natural Science Foundation of Jiangsu Province, Nanjing University of Posts and Telecommunications, Jiangsu Science and Technology Department, Beijing Municipal Natural Science Foundation
Affordable and clean energy
Openalex Percentile: Top 1%
Advanced Battery Materials and Technologies
11.69
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