电催化剂
催化作用
氧化还原
硫黄
化学
金属
吸附
过渡金属
无机化学
化学稳定性
化学反应
分离器(采油)
化学工程
催化循环
半反应
化学键
动力学
功能群
反应机理
化学动力学
化学改性
活动站点
主组元素
化学反应工程
电池(电)
作者
Shengjie Wei,Xingxin Hu,Rongyan Yang,Baixiong Liu,Qi Kang,Xijun Wang,Yuxiang Hu
标识
DOI:10.1002/ange.202517190
摘要
Abstract Precisely constructing atomic engineering of catalytic site and thus accelerating sulfur redox kinetics are meaningful but challenging for energy storage and conversion. Herein, the catalytic nano‐reactor engineering containing Fe‐N 4 catalytic site and the adjacent PO chemical group as synergistic catalytic site (Fe‐N 4 /CNPO) was first designed for Li‐S batteries with remarkably improved performance. The adjacent PO chemical group of Fe‐N 4 site in catalytic nano‐reactor simultaneously strengthened the adsorption of lithium polysulfides and facilitated the fracture of Li─S bonds by Li─O interaction, thus lowering the free energy change of potential‐determining step and accelerating sulfur redox kinetics, which was further verified via density functional theory calculation. The optimized Fe‐N 4 /CNPO modified separator exhibited much higher battery capacity of 1322.1 mAh g −1 at 0.2 C and enhanced long‐term stability (low capacity decay of 0.08% per cycle over 500 cycles at 1.0 C). This work demonstrated the enormous potentiality of catalytic nano‐reactor engineering containing metal single‐atom catalytic site and chemical group as synergistic catalytic site for accelerating sulfur redox in metal‐sulfur batteries.
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