材料科学
锂(药物)
电解质
电极
快离子导体
金属
化学工程
碱金属
可逆氢电极
半电池
无机化学
物理化学
参比电极
工作电极
冶金
化学
医学
有机化学
工程类
内分泌学
作者
Xinshuang Chang,Wei Weng,Mengqi Li,Ming Wu,George Z. Chen,Kam Loon Fow,Xiayin Yao
标识
DOI:10.1021/acsami.3c03242
摘要
Lithium (Li) metal has an ultrahigh specific capacity in theory with an extremely negative potential (versus hydrogen), receiving extensive attention as a negative electrode material in batteries. However, the formation of Li dendrites and unstable interfaces due to the direct Li metal reaction with solid sulfide-based electrolytes hinders the application of lithium metal in all-solid-state batteries. In this work, we report the successful fabrication of a LiAlO2 interfacial layer on a Li/Li10GeP2S12 interface through magnetic sputtering. As LiAlO2 can be a good Li+ ion conductor but an electronic insulator, the LiAlO2 interface layer can effectively suppress Li dendrite growth and the severe interface reaction between Li and Li10GeP2S12. The Li@LiAlO2 200 nm/Li10GeP2S12/Li@LiAlO2 200 nm symmetric cell can remain stable for 3000 h at 0.1 mA cm-2 under 0.1 mAh cm-2. Moreover, unlike the rapid capacity decay of a cell with a pristine lithium negative electrode, the Li@LiAlO2 200 nm/Li10GeP2S12/LiCoO2@LiNbO3 cell delivers a reversible capacity of 118 mAh g-1 and a high energy efficiency of 96.6% after 50 cycles. Even at 1.0 C, the cell with the Li@LiAlO2 200 nm electrode can retain 95% of its initial capacity after 800 cycles.
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