阴极
阳极
电池(电)
电化学
材料科学
钠
纳米技术
钠离子电池
降级(电信)
枝晶(数学)
化学工程
电极
化学
电气工程
冶金
工程类
物理
法拉第效率
物理化学
功率(物理)
量子力学
数学
几何学
作者
Zhen Xiong,Xuyuan Nie,Binwei Zhang,Zidong Wei
标识
DOI:10.1002/batt.202300503
摘要
Abstract Room temperature sodium‐sulfur (RT‐Na/S) battery is regarded as a promising next‐generation battery system because of their high theoretical specific capacity, and abundant availability of anodes and cathodes. Nevertheless, the direct use of sodium metal could result in the dendrite growth, causing the safety concerns. Interestingly, employing Na 2 S as the cathode materials can be paired with Na‐free anode to effectively avoid the problem of dendrite growth. However, the poor electronic conductivity of Na 2 S and the sluggish kinetic conversion to sodium polysulfides can lead to high initial charge activation barriers and rapid capacity degradation, thereby constraining their practical application. In this concept, the electrochemical mechanism of Na 2 S cathode is summarized to present the potential for RT‐Na/S batteries. Additionally, recent advances on Na 2 S cathodes have been discussed in detail with an emphasis on functionalized matrix, morphology modulation, and optimizing cell structure. Finally, the future opportunities and challenges for the development of Na 2 S cathode based RT‐Na/S batteries are proposed.
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