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用于高压和坚固的 Li/LiCoO 电池的具有空间限制增塑剂的原位聚合 1,3-二氧戊环固态电解质。

In-Situ-Polymerized 1,3-Dioxolane Solid-State Electrolyte with Space-Confined Plasticizers for High-Voltage and Robust Li/LiCoO Batteries.

机构信息

Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, People's Republic of China.

College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2023 Jun 7;15(22):26834-26842. doi: 10.1021/acsami.3c04234. Epub 2023 May 24.

Abstract

In-situ-polymerized solid-state electrolytes can significantly improve the interfacial compatibility of Li metal batteries. Typically, in-situ-polymerized 1,3-dioxolane electrolyte (PDOL) exhibits good compatibility with Li metal. However, it still suffers from the narrow electrochemical window (4.1 V), limiting the application of high-voltage cathodes. Herein, a novel modified PDOL (PDOL-F/S) electrolyte with an expanded electrochemical window of 4.43 V and a considerable ionic conductivity of 1.95 × 10 S cm is developed by introducing high-voltage stable plasticizers (fluoroethylene carbonate and succinonitrile) to its polymer network. The space-confined plasticizers are beneficial to construct a high-quality cathode-electrolyte interphase, hindering the decomposition of lithium salts and polymers in electrolytes at high voltage. The as-assembled Li|PDOL-F/S|LiCoO battery delivers superior cycling stability (capacity retention of 80% after 400 cycles) at 4.3 V, superior to that of pristine PDOL (3% after 120 cycles). This work provides new insights into the design and application of high-voltage solid-state lithium metal batteries by in situ polymerization.

摘要

原位聚合固态电解质可以显著改善锂金属电池的界面相容性。通常,原位聚合的 1,3-二氧戊环电解质(PDOL)与锂金属具有良好的相容性。然而,它仍然受到 4.1 V 窄电化学窗口的限制,限制了高压阴极的应用。在此,通过将高压稳定的增塑剂(氟代碳酸乙烯酯和丁二腈)引入聚合物网络,开发了一种具有 4.43 V 扩展电化学窗口和相当高离子电导率 1.95×10 S cm 的新型改性 PDOL(PDOL-F/S)电解质。受限的增塑剂有利于构建高质量的阴极-电解质界面,阻碍电解质中锂盐和聚合物在高压下的分解。组装的 Li|PDOL-F/S|LiCoO 电池在 4.3 V 下具有优异的循环稳定性(400 次循环后容量保持率为 80%),优于原始 PDOL(120 次循环后为 3%)。这项工作通过原位聚合为设计和应用高压固态锂金属电池提供了新的见解。

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