固溶体
材料科学
硫黄
锂硫电池
相(物质)
电池(电)
锂(药物)
化学工程
无机化学
化学
冶金
功率(物理)
热力学
有机化学
物理
工程类
内分泌学
医学
作者
Xiang Li,Lixia Yuan,Dezhong Liu,Jingwei Xiang,Zhen Li,Yunhui Huang
出处
期刊:Small
[Wiley]
日期:2022-02-26
卷期号:18 (43)
被引量:34
标识
DOI:10.1002/smll.202106970
摘要
Abstract The lithium–sulfur (Li–S) battery is considered as one of the most promising options because the redox couple has almost the highest theoretical specific energy (2600 Wh kg −1 ) among all solid anode‐cathode candidates for rechargeable batteries. The “solid–liquid–solid” mechanism has become a dominating phase transformation process since it was first reported, although this cathode mode suffers from a tough “shuttle” phenomenon due to the dissolution of the soluble intermediate polysulfides generated during the charging‐discharging process, which causes rapid loss of energy‐bearing material and shortened lifespan. For decades, tremendous efforts have been made to restrict the shuttle effect. Changing sulfur conversion to “solid–solid” mode or “quasi‐solid” mode, which successfully exceed the limit of the dissolution of the intermediates, and may address the root of the problem. In this review, the main focus is on the fundamental chemistry of the “solid‐solid” and “quasi‐solid” phase transformation of the sulfur cathode. First, the strategies of sulfur immobilization in “solid–liquid–solid” multi‐phase conversions as well as the pivotal influence factors for the electrochemical conversion process are briefly introduced. Then, the different routes are summarized to realize the “solid–solid” and “quasi‐solid” redox mechanisms. Finally, a perspectives on building high‐energy‐density Li–S batteries are provided.
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