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用于固态锂金属电池的纳米充电复合聚合物电解质的锂离子动态界面工程

Lithium-Ion Dynamic Interface Engineering of Nano-Charged Composite Polymer Electrolytes for Solid-State Lithium-Metal Batteries.

作者信息

Lv Shanshan, Wang Jingwen, Zhai Yuanming, Chen Yu, Yang Jiarui, Zhu Zhiwei, Peng Rui, Fu Xuewei, Yang Wei, Wang Yu

机构信息

College of Polymer Science and Engineering, National Key Laboratory of Advanced Polymer Materials, Sichuan University, Chengdu, 610065, People's Republic of China.

Analytical and Testing Center, Sichuan University, Chengdu, 610065, People's Republic of China.

出版信息

Nanomicro Lett. 2025 Aug 29;18(1):46. doi: 10.1007/s40820-025-01899-7.

DOI:10.1007/s40820-025-01899-7
PMID:40879855
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12397479/
Abstract

Composite polymer electrolytes (CPEs) offer a promising solution for all-solid-state lithium-metal batteries (ASSLMBs). However, conventional nanofillers with Lewis-acid-base surfaces make limited contribution to improving the overall performance of CPEs due to their difficulty in achieving robust electrochemical and mechanical interfaces simultaneously. Here, by regulating the surface charge characteristics of halloysite nanotube (HNT), we propose a concept of lithium-ion dynamic interface (Li-DI) engineering in nano-charged CPE (NCCPE). Results show that the surface charge characteristics of HNTs fundamentally change the Li-DI, and thereof the mechanical and ion-conduction behaviors of the NCCPEs. Particularly, the HNTs with positively charged surface (HNTs) lead to a higher Li transference number (0.86) than that of HNTs (0.73), but a lower toughness (102.13 MJ m for HNTs and 159.69 MJ m for HNTs). Meanwhile, a strong interface compatibilization effect by Li is observed for especially the HNTs-involved Li-DI, which improves the toughness by 2000% compared with the control. Moreover, HNTs are more effective to weaken the Li-solvation strength and facilitate the formation of LiF-rich solid-electrolyte interphase of Li metal compared to HNTs. The resultant Li|NCCPE|LiFePO cell delivers a capacity of 144.9 mAh g after 400 cycles at 0.5 C and a capacity retention of 78.6%. This study provides deep insights into understanding the roles of surface charges of nanofillers in regulating the mechanical and electrochemical interfaces in ASSLMBs.

摘要

复合聚合物电解质(CPEs)为全固态锂金属电池(ASSLMBs)提供了一种很有前景的解决方案。然而,具有Lewis酸碱表面的传统纳米填料对提高CPEs的整体性能贡献有限,因为它们难以同时实现强大的电化学和机械界面。在此,通过调节埃洛石纳米管(HNT)的表面电荷特性,我们提出了纳米充电CPE(NCCPE)中的锂离子动态界面(Li-DI)工程概念。结果表明,HNTs的表面电荷特性从根本上改变了Li-DI,进而改变了NCCPEs的机械和离子传导行为。特别是,表面带正电的HNTs(HNTs)导致锂迁移数(0.86)高于HNTs(0.73),但韧性较低(HNTs为102.13 MJ m,HNTs为159.69 MJ m)。同时,对于特别是涉及HNTs的Li-DI,观察到Li具有很强的界面增容效果,与对照相比,其韧性提高了2000%。此外,与HNTs相比,HNTs在削弱锂溶剂化强度和促进锂金属富LiF固体电解质界面形成方面更有效。由此得到的Li|NCCPE|LiFePO电池在0.5 C下循环400次后容量为144.9 mAh g,容量保持率为78.6%。这项研究为理解纳米填料表面电荷在调节ASSLMBs中的机械和电化学界面方面的作用提供了深刻见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af80/12397479/df8f0007400b/40820_2025_1899_Fig7_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af80/12397479/df8f0007400b/40820_2025_1899_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af80/12397479/a06f73930499/40820_2025_1899_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af80/12397479/fce4c6336c6c/40820_2025_1899_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af80/12397479/df8f0007400b/40820_2025_1899_Fig7_HTML.jpg

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本文引用的文献

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Stable Cycling of All-Solid-State Lithium Batteries Enabled by Cyano-Molecular Diamond Improved Polymer Electrolytes.
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