Enhancing interfacial stability in sulfide all-solid-state batteries through surface dual-doping of Zr and F in Ni-rich cathodes

被引:8
|
作者
Feng, Daoyan [1 ,2 ]
Liu, Yu [1 ]
Zhao, Chen [2 ]
Su, Han [1 ]
Kong, Xia [2 ]
Zhong, Yu [1 ]
Wang, Junzhang [1 ]
Xu, Zhou [1 ]
Wang, Xiuli [1 ]
Guo, Xingzhong [1 ]
Lee, Jonghee [2 ]
Tu, Jiangping [1 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon & Adv Semicond Mat, Hangzhou 310058, Peoples R China
[2] Ningbo Ronbay New Energy Technol Co Ltd, Ningbo 315400, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Sulfide all -solid -state battery; Ni-rich layered cathode; Interfacial stability; Surface doping; TOTAL-ENERGY CALCULATIONS; LITHIUM-ION TRANSPORT; PERFORMANCE; LINI0.8CO0.15AL0.05O2; ELECTROLYTE; CAPACITY;
D O I
10.1016/j.cej.2023.147184
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Achieving a stable interface between sulfide solid-state electrolytes (SSEs) and high-voltage Ni-rich oxide cathodes is crucial for enhancing the electrochemical performance of all-solid-state batteries (ASSBs). However, addressing the interface challenges through surface coating modifications remains a significant hurdle. In this work, a straightforward modification approach is proposed to achieve a highly stable interface by surface dual doping of Zr and F in LiNi0.83Co0.12Mn0.05O2 (NCM83) cathodes via acid washing followed by annealing. First-principle calculations demonstrate the thermodynamic stability of Zr-F doped NCM83, effectively inhibiting the formation of unfavorable interfaces with decomposition products. The modified NCM83-1% ZrF cathode exhibits exceptional long-cycle stability, retaining 85.1% of its capacity after 1000 cycles at 0.5C rate. This simple and scalable modification strategy offers a new perspective for the design of high-performance sulfide-based ASSBs.
引用
收藏
页数:8
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