材料科学
阳极
金属锂
合金
锂(药物)
自行车
固态
金属
冶金
化学工程
电极
工程物理
物理化学
考古
化学
内分泌学
工程类
历史
医学
作者
Linxue Zhang,Dehua Xu,Hao Chen,Rui Li,Zhenglin Hu,Bohua Wen,Aosai Chen,Xingjiang Liu,Jiayan Luo,Aoxuan Wang
标识
DOI:10.1002/adfm.202416013
摘要
Abstract All solid state lithium metal batteries (ASSLMBs) with enhanced energy density has driven the exploration of Li‐alloy anodes such as Li‐Mg alloy owing to its solid‐solution structure and high theoretical specific capacity. But the Li atom diffusion limitation on Li‐Mg electrode surface further leads to sluggish atoms transport dynamics. Herein, single‐crystalline (110)‐oriented Li 0.9 Mg 0.1 (denoted as LiMg(110)) anode is obtained by a tailored melt‐annealing procedure to tackle the above issues. Theoretical analyses and experimental results demonstrate that the crystallographic structural (110) orientation of LiMg anode can facilitate Li atom diffusion and guarantee the electrode stability during deep cycling. As a result, the LiMg(110) electrode exhibits longer cycle life with lower overpotential than polycrystalline LiMg at high current densities and areal capacities in symmetric cells. A critical current density (CCD) at the forefront of 2.5 mA cm −2 is achieved in Li 3 InCl 6 (LIC) solid‐state system. The ASSLMB with high areal capacity (3.8 mAh cm −2 ), high current density (0.76 mA cm −2 ), and low negative/positive capacity N/P ratio (2.14) achieves exceptional cyclability over 160 cycles. The outcomes highlight a promising crystallographic regulation strategy toward practical applications of high‐performance lithium metal batteries.
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