合金
锂(药物)
材料科学
阳极
扩散
电池(电)
固溶体
动能
Atom(片上系统)
降水
过渡金属
化学物理
化学工程
热力学
物理化学
冶金
化学
电极
催化作用
内分泌学
功率(物理)
气象学
嵌入式系统
工程类
物理
医学
量子力学
生物化学
计算机科学
作者
Yang Lu,Chen‐Zi Zhao,Rui Zhang,Hong Yuan,Li‐Peng Hou,Zhongheng Fu,Xiang Chen,Jia‐Qi Huang,Qiang Zhang
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2021-09-17
卷期号:7 (38)
被引量:154
标识
DOI:10.1126/sciadv.abi5520
摘要
The stable cycling of energy-dense solid-state batteries is highly relied on the kinetically stable solid-state Li alloying reactions. The Li metal precipitation at solid-solid interfaces is the primary cause of interface fluctuations and battery failures, whose formation requires a clear mechanism interpretation, especially on the key kinetic short board. Here, we introduce the lithium alloy anode as a model system to quantify the Li kinetic evolution and transition from the alloying reaction to the metal deposition in solid-state batteries, identifying that there is a carrier transition from Li atoms to Li vacancies during lithiation processes. The rate-determining step is charge transfer or Li atom diffusion at different lithiation stages.
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