材料科学
微尺度化学
电解质
阴极
电化学
拉曼光谱
锂(药物)
化学工程
纳米技术
化学物理
物理化学
电极
工程类
化学
数学教育
内分泌学
物理
光学
医学
数学
作者
Yuexian Song,Yang Shi,Jing Wan,Bing Liu,Li‐Jun Wan,Rui Wen
标识
DOI:10.1002/aenm.202000465
摘要
Abstract Solid‐state lithium–sulfur batteries (SSLSBs) are highly appealing for electrochemical energy devices because of their promising theoretical energy density. An intensive acquaintance of SSLS interfacial behavior is of importance in gaining fundamental knowledge of working/failure mechanisms and clarifying further optimized design of advanced batteries. Herein, a direct visualization of the evolution of both component and structure is present inside a working SSLSB. In situ Raman spectroscopy clearly sheds light on the potential‐dependent evolution of sulfur speciation via subtly fabricating the electrochemical cell. Moreover, the real‐time optical microscopic views show that the irreversible structure deformation of solid‐state electrolytes (SSEs), which results from the decomposition of dissolved polysulfides (PSs) and gas generation inside the SSE, directly causes the fracture of sulfur cathode with the cycling times increasing. Furthermore, by an atomic force microscopy study, the evolving structure and dynamic behavior of SSEs are directly captured at the nano/microscale and further elucidate the PS shuttling determining the mechanism stability of electrolyte. This work provides a straightforward monitoring of the compositional and morphological evolution, which contributes one to exploring the failure mechanisms and interfacial reactions for the cell performance enhancement.
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