固态
材料科学
功率(物理)
化学
热力学
物理
物理化学
作者
Y. Sun,Yanbin Ning,Zhuomin Qiang,Lizhi Xiang,Qingsong Liu,Chaoqun Zhang,Guoce Quan,Yan Zhang,Biao Deng,Geping Yin,Tiefeng Liu,Jiajun Wang,Shuaifeng Lou
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-03-11
卷期号:64 (36): e202502169-e202502169
被引量:4
标识
DOI:10.1002/anie.202502169
摘要
In solid-state lithium-ion batteries, the fraction of active materials involved in electrode electrochemistry reduces with the increase of electrode thickness. Conventional wisdom suggests that the degree of reaction linearly decreases toward the current collector as in lithium-ion batteries, which is, however, limited by the high difficulty of experimental capture of operando charge and mass transport. Electrode dynamics simulations can provide space visualization but are usually based on simplified models. Herein, we build digital-twin electrodes with digital-space voxel microstructure based on synchrotron tomography, which transforms the electrode architecture from real space to digital space for the construction of precision models. From the digital model-driven simulation, we find an "lithium trapping" effect, stemming from susceptible lithium stuck in the solid electrolyte, triggers an inadequate reaction of the intermediate region of electrodes. Then, we construct locally accelerated ion paths activating the lithium trapping, indicating that this strategy can significantly guide the sustainable battery design for next-generation energy storage.
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