Unveiling the Mechanical and Electrochemical Evolution of Nanosilicon Composite Anodes in Sulfide‐Based All‐Solid‐State Batteries

材料科学 阳极 氧烷 复合数 硫化物 化学工程 电解质 电化学 扫描电子显微镜 碳纤维 复合材料 电极 光谱学 冶金 物理化学 化学 量子力学 物理 工程类
作者
Daxian Cao,Tongtai Ji,Avtar Singh,Seong‐Min Bak,Yonghua Du,Xianghui Xiao,Hongyi Xu,Juner Zhu,Hongli Zhu
出处
期刊:Advanced Energy Materials [Wiley]
卷期号:13 (14) 被引量:120
标识
DOI:10.1002/aenm.202203969
摘要

Abstract The utilization of silicon anodes in all‐solid‐state lithium batteries provides good prospects for facilitating high energy density. However, the compatibility of sulfide solid‐state electrolytes (SEs) with Si and carbon is often questioned due to potential decomposition. Herein, operando X‐ray absorption near‐edge structure (XANES) spectroscopy, ex situ scanning electron microscopy (SEM), and ex situ X‐ray nanotomography (XnT) are utilized to investigate the chemistry and structure evolution of nano‐Si composite anodes. Results from XANES demonstrate a partial decomposition of SEs during the first lithiation stage, which is intensified by the presence of carbon. Nevertheless, the performances of first three cycles in Si–SE–C are stable, which proves that the generated media is ionically conductive. XnT and SEM results show that the addition of SEs and carbon improves the structural stability of the anode, with fewer pores and voids. A chemo‐elasto‐plastic model reveals that SEs and carbon buffer the volume expansion of Si, thus enhancing mechanical stability. The balance between the pros and cons of SEs and carbon in enhancing reaction kinetics and structural stability enables the Si composite anode to demonstrate the highest Si utilization with higher specific capacities and a better rate than pure Si and Si composite anodes with only SEs.
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