电化学
催化作用
电池(电)
过渡金属
价(化学)
化学
电极
化学工程
材料科学
纳米技术
物理化学
物理
有机化学
功率(物理)
量子力学
工程类
作者
Rong Zhou,Yongqiang Ren,Weixin Li,Meng Guo,Yinan Wang,Haixin Chang,Xin Zhao,Wei Hu,Guowei Zhou,Shaonan Gu,Shaonan Gu,Shaonan Gu
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-05-18
卷期号:63 (31): e202405417-e202405417
被引量:49
标识
DOI:10.1002/anie.202405417
摘要
Abstract Lithium‐sulfur (Li−S) batteries have many advantages but still face problems such as retarded polysulfides redox kinetics and Li dendrite growth. Most reported single atom catalysts (SACs) for Li−S batteries are based on d ‐band transition metals whose d orbital constitutes active valence band, which is inclined to occur catalyst passivation. SACs based on 4 f inner valence orbital of rare earth metals are challenging for their great difficulty to be activated. In this work, we design and synthesize the first rare earth metal Sm SACs which has electron‐rich 4 f inner orbital to promote catalytic conversion of polysulfides and uniform deposition of Li. Sm SACs enhance the catalysis by the activated 4 f orbital through an f‐d‐p orbital hybridization. Using Sm‐N 3 C 3 modified separators, the half cells deliver a high capacity over 600 mAh g −1 and a retention rate of 84.3 % after 2000 cycles. The fabricated Sm‐N 3 C 3 ‐Li|Sm‐N 3 C 3 @PP|S/CNTs full batteries can provide an ultra‐stable cycling performance of a retention rate of 80.6 % at 0.2 C after 100 cycles, one of the best full Li−S batteries. This work provides a new perspective for the development of rare earth metal single atom catalysis in electrochemical reactions of Li−S batteries and other electrochemical systems for next‐generation energy storage.
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