材料科学
锂硫电池
催化作用
硫黄
电池(电)
Atom(片上系统)
锂(药物)
无机化学
化学工程
纳米技术
冶金
有机化学
热力学
计算机科学
嵌入式系统
医学
物理
工程类
内分泌学
功率(物理)
化学
作者
Yi Li,Zhaoyang Chen,Xinyu Zhong,Tiehan Mei,Zhao Li,Yue Liang,Jin‐Lin Yang,Hong Jin Fan,Maowen Xu
标识
DOI:10.1002/adfm.202412279
摘要
Abstract The coordination environment is crucial to the electrocatalytic activity of single‐atom catalysts (SACs). Although substituting N atoms in traditional transition metal‐nitrogen (TM‐N 4 ) configuration with other non‐metal atoms has been reported, its specific role in sulfur electrochemical reactions has not been sufficiently investigated. Herein, a Co‐P 2 N 2 SACs configuration is fabricated to investigate the mechanistic differences compared to Co‐N 4 in sulfur reduction/oxidation. This configuration enhances the electron transfer with Li 2 S 6 , where the electrons tend to aggregate between P and Li atoms as two separate parts rather than a single merged zone as observed in symmetric Co‐N 4 SACs. This process facilitates polysulfide decomposition and promotes Li 2 S nucleation/oxidation. Furthermore, the CoPNC interlayer effectively suppresses cell self‐discharge and Li anode corrosion due to polysulfide shuttling. Li‐Li symmetrical cell incorporated with the CoPNC interlayer achieves a prolonged lifespan exceeding 1000 h, and Li‐S full cell delivers a discharge capacity of more than 1500 mAh g −1 . This research provides insights into how the geometric configuration of SACs influences the performance of conversion‐type batteries.
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