材料科学
阴极
涂层
固态
纳米技术
化学工程
光电子学
工程物理
化学
物理化学
工程类
作者
Wuyan Zhao,Ruizhuo Zhang,Fucheng Ren,Leonhard Karger,Sören L. Dreyer,Jing Lin,Yuan Ma,Yong Cheng,Avnish Singh Pal,Martin Velazquez-Rizo,Ali Ahmadian,Ziyan Zhang,Philipp Müller,Jürgen Janek,Yong Yang,Aleksandr Kondrakov,Torsten Brezesinski
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-01-29
标识
DOI:10.1021/acsnano.4c14322
摘要
Improving interfacial stability between cathode active material (CAM) and solid electrolyte (SE) is vital for developing high-performance all-solid-state batteries (ASSBs), with compatibility issues among the cell components representing a major challenge. CAM surface coating with a chemically inert ion conductor is a promising approach to suppress side reactions occurring at the cathode interfaces. Another strategy to mitigate mechanical degradation involves utilizing single-crystalline particle morphologies. Their more robust bulk structure and lower tortuosity for charge transport, compared to polycrystalline (PC) CAMs, can significantly enhance cyclability in ASSBs. Herein, we coated a LiNbO3 protective layer onto the free surface of quasi single-crystalline LiNi0.83Co0.12Mn0.05O2 (SC83) particles. Pellet-stack ASSB cells using the LiNbO3@SC83 CAM and argyrodite Li6PS5Cl as SE showed a capacity retention of 88% after 1000 cycles at the 1 C rate, compared to only 71% for the uncoated counterpart and far superior to that of LiNbO3@PC83 (30%). The effectiveness of LiNbO3 coating and the SC-NCM nature in mitigating electro-chemo-mechanical degradation was studied by combining modeling and physical/electrochemical characterizations. We demonstrate that the capacity decay at fast charge is due primarily to the mechanical degradation of CAM particles, while it is strongly determined by CAM|SE interfacial reactions under slow-charging conditions.
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