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增强的电化学稳定性和离子传输速率:一种用于高性能全固态锂硫电池的聚合物/陶瓷复合电解质。

Enhanced electrochemical stability and ion transfer rate: A polymer/ceramic composite electrolyte for high-performance all-solid-state lithium-sulfur batteries.

作者信息

Shao Yaxin, Mei Yuhan, Liu Tao, Li Zhenhu, Zhang Yulin, Liu Shuangyi, Liu Yuping

机构信息

Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing 400714, PR China; Chongqing School, University of Chinese Academy of Sciences, Chongqing 400714, PR China; University of Chinese Academy of Sciences, Beijing 10049, PR China.

Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing 400714, PR China; Chongqing School, University of Chinese Academy of Sciences, Chongqing 400714, PR China; University of Chinese Academy of Sciences, Beijing 10049, PR China.

出版信息

J Colloid Interface Sci. 2025 Jan 15;678(Pt C):682-689. doi: 10.1016/j.jcis.2024.09.088. Epub 2024 Sep 13.

DOI:10.1016/j.jcis.2024.09.088
PMID:39307057
Abstract

All-solid-state (ASS) lithium-sulfur (LiS) batteries utilizing composite polymer electrolytes (CPEs) represent a promising avenue in the domain of electric vehicles and large-scale energy storage systems, leveraging the combined benefits of polymer electrolytes (PEs) and ceramic electrolytes (CEs). However, the inherent weak interface compatibility between PEs and CEs often leads to phase separation, thereby impeding the transposition of Li. In this study, the trimethoxy-[3-(2-methoxyethoxy)propyl]silane (TM-MES) is introduced as a chemical agent to form bonds with polyethylene oxide (PEO) and LiGePS (LGPS), resulting in the development of a novel composite polymer electrolyte (CPE). This innovative approach mitigates phase separation between PEs and CEs while concurrently enhancing the protective capabilities of LGPS against decomposition at the interfaces of both the Li anode and sulfur cathode. Moreover, the CPE exhibits superior mechanical toughness, an expanded electrochemical window, and elevated ionic conductivity. In the symmetric cell, it demonstrates an extended operational lifespan exceeding 1800 h, and the current density can reach up to 1.05 mA/cm. Furthermore, the initial discharge capacity of ASS LiS batteries utilizing CPE attains 1227 mAh/g and maintains a capacity of 904 mAh/g after 100 cycles. Notably, a high-energy-density of 2454 Wh/kg is achieved based on the sulfur cathode.

摘要

采用复合聚合物电解质(CPE)的全固态(ASS)锂硫(LiS)电池,融合了聚合物电解质(PE)和陶瓷电解质(CE)的优势,在电动汽车和大规模储能系统领域展现出广阔前景。然而,PE与CE之间固有的弱界面相容性常导致相分离,阻碍锂的迁移。本研究引入三甲氧基-[3-(2-甲氧基乙氧基)丙基]硅烷(TM-MES)作为化学试剂,使其与聚环氧乙烷(PEO)和锂锗磷硫(LGPS)形成化学键,从而开发出一种新型复合聚合物电解质(CPE)。这种创新方法减轻了PE与CE之间的相分离,同时增强了LGPS在锂阳极和硫阴极界面处抵抗分解破坏的能力。此外,该CPE具有优异的机械韧性、更宽的电化学窗口和更高的离子电导率。在对称电池中,其运行寿命超过1800小时,电流密度可达1.05 mA/cm²。此外,采用CPE的ASS LiS电池的初始放电容量达到1227 mAh/g,100次循环后容量保持在904 mAh/g。值得注意的是,基于硫阴极实现了2454 Wh/kg的高能量密度。

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