阳极
材料科学
电极
固态
化学工程
工程物理
国家(计算机科学)
光电子学
纳米技术
化学
物理化学
计算机科学
算法
工程类
作者
Wei-xiao Ji,Xiaoxiao Zhang,Miao Liu,Tianyao Ding,Huainan Qu,Dantong Qiu,Dong Zheng,Deyang Qu
标识
DOI:10.1016/j.ensm.2022.10.003
摘要
The development of all-solid-state Li–S batteries has been greatly impeded by dendrite growth and dendrite penetration, which are both related to the Li metal anode. As a compromised alternative, we report lithium silicide (LixSi) as a dendrite-free and high-capacity anode with Li source. The as-synthesized LixSi is relatively soft, highly electronically conductive, and with a high Li diffusivity. These distinctive properties make LixSi anode viable as an “all-electrochem-active” electrode (consisted of 100 wt.% LixSi). Compared with the typical composite electrode, the all-electrochem-active electrode not merely maximizes the electrode-level energy density but also minimizes the electrolyte-related interfacial degradation. LixSi symmetric cell demonstrates a reversible cycling at 4 mA cm–2 for over 320 h. Stress change and morphological evolution of the LixSi electrode are investigated upon dealloying/alloying. When paired with a S cathode (active mass loading of 3 mg cm–2), LixSi–S full cell shows a good cycling behavior over 500 cycles and rate performance (69% capacity retained at 1.2C) even at 25 °C.
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