级联
催化作用
多硫化物
反键分子轨道
化学
材料科学
电解质
电极
锂(药物)
化学工程
动力学
无机化学
纳米技术
原子轨道
Atom(片上系统)
掺杂剂
阴极
原位
呼吸
活动站点
燃料电池
作者
Yan Zhang,Wei Zhao,Yanbin Ning,Shenglu Geng,Shengwei Dong,Chong Wang,Feiyun Sun,Geping Yin,Shuaifeng Lou
标识
DOI:10.1002/anie.202524645
摘要
Abstract High‐energy‐density lithium–sulfur batteries exhibit obvious kinetics differences involving multistep reactions, making it hard to realize constantly high‐efficient polysulfide conversion during the full charging/discharging Herein, we propose a concept of Li + ‐respiration‐effect‐induced cascade catalysis through taking full advantage of dynamic active sites from in situ potential‐modulated TiNb 2 O 7 . The Li + respiration effect activates the lattice O atom and regulates the antibonding orbitals filling, triggering an electrochemical‐dominated switchable catalytic for sequential conversion of intermediates. As a result, the Li–S cell displays a good cycling stability and wide‐temperature ability from −30 to +60 °C. A flexible pouch cell maintains a capacity retention of 94.6% after 120 cycles. Our discovery provides a fire‐new perspective in electrochemically reconstructed catalysis for wide‐temperature‐tolerant Li − S batteries.
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