硫黄
氧化还原
硫化钴
钴
化学
阴极
硫化物
电子转移
钠
化学工程
无机化学
电极
光化学
电化学
有机化学
物理化学
工程类
作者
Yaojie Lei,Can Wu,Xinxin Lu,Weibo Hua,Shaobo Li,Yaru Liang,Hanwen Liu,Wei‐Hong Lai,Qinfeng Gu,Xiaolan Cai,Nana Wang,Yunxiao Wang,Shulei Chou,Huan Liu,Guoxiu Wang,Shi Xue Dou
标识
DOI:10.1002/anie.202200384
摘要
It is vital to dynamically regulate S activity to achieve efficient and stable room-temperature sodium-sulfur (RT/Na-S) batteries. Herein, we report using cobalt sulfide as an electron reservoir to enhance the activity of sulfur cathodes, and simultaneously combining with cobalt single atoms as double-end binding sites for a stable S conversion process. The rationally constructed CoS2 electron reservoir enables the straight reduction of S to short-chain sodium polysulfides (Na2 S4 ) via a streamlined redox path through electron transfer. Meanwhile, cobalt single atoms synergistically work with the electron reservoir to reinforce the streamlined redox path, which immobilize in situ formed long-chain products and catalyze their conversion, thus realizing high S utilization and sustainable cycling stability. The as-developed sulfur cathodes exhibit a superior rate performance of 443 mAh g-1 at 5 A g-1 with a high cycling capacity retention of 80 % after 5000 cycles at 5 A g-1 .
科研通智能强力驱动
Strongly Powered by AbleSci AI