材料科学
阳极
电解质
电化学
卤化物
成核
枝晶(数学)
锂(药物)
化学工程
金属
沉积(地质)
纳米技术
电极
无机化学
冶金
物理化学
热力学
医学
化学
物理
几何学
数学
工程类
内分泌学
古生物学
沉积物
生物
作者
Hui Duan,Changhong Wang,Ruizhi Yu,Weihan Li,Jiamin Fu,Xiaofei Yang,Xiaoting Lin,Matthew Zheng,Xiaona Li,Sixu Deng,Xiaoge Hao,Ruying Li,Jiantao Wang,Huan Huang,Xueliang Sun
标识
DOI:10.1002/aenm.202300815
摘要
Abstract Constructing a 3D lithium metal anode has been demonstrated to be the most effective strategy to address its dendrite issue in liquid batteries. However, this promising approach has proved challenging to inherit in all‐solid‐state Li metal batteries (ASSLMBs) because of the rigidity of inorganic solid electrolytes (SEs), which constrains interfacial solid–solid ionic contact. Herein, a 3D Li anode is in situ constructed for ASSLMBs by spontaneous chemical reactions between halide SEs and Li metal. The in situ formed Li–Al alloys and well‐maintained sulfide SEs inside the 3D structure serve as continuous electron and Li + transport pathways and facilitate the homogenous distribution of charge carriers. The lithiophilic Li alloy can regulate Li deposition behavior and enable uniform Li nucleation and deposition. Both the Li||Li symmetric and full batteries exhibit good electrochemical performance at high current density. This work provides a universal strategy and new insight perspective to construct 3D Li for high‐performance ASSLMBs.
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