电解质
阳极
成核
电池(电)
降级(电信)
晶界
材料科学
微观结构
无定形固体
再结晶(地质)
纳米尺度
电化学
化学工程
化学物理
纳米技术
冶金
化学
工程类
物理
热力学
结晶学
物理化学
计算机科学
电极
功率(物理)
古生物学
生物
电信
作者
Se‐Ho Kim,Kang Dong,Huan Zhao,Ayman A. El‐Zoka,Xuyang Zhou,Eric Woods,Finn Giuliani,Ingo Manke,Dierk Raabe,Baptiste Gault
标识
DOI:10.1021/acs.jpclett.2c02236
摘要
To advance the understanding of the degradation of the liquid electrolyte and Si electrode, and their interface, we exploit the latest developments in cryo-atom probe tomography. We evidence Si anode corrosion from the decomposition of the Li salt before charge–discharge cycles even begin. Volume shrinkage during delithiation leads to the development of nanograins from recrystallization in regions left amorphous by the lithiation. The newly created grain boundaries facilitate pulverization of nanoscale Si fragments, and one is found floating in the electrolyte. P is segregated to these grain boundaries, which confirms the decomposition of the electrolyte. As structural defects are bound to assist the nucleation of Li-rich phases in subsequent lithiations and accelerate the electrolyte's decomposition, these insights into the developed nanoscale microstructure interacting with the electrolyte contribute to understanding the self-catalyzed/accelerated degradation Si anodes and can inform new battery designs unaffected by these life-limiting factors.
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