Lei Yaojie, Wu Can, Lu Xinxin, Hua Weibo, Li Shaobo, Liang Yaru, Liu Hanwen, Lai Wei-Hong, Gu Qinfeng, Cai Xiaolan, Wang Nana, Wang Yun-Xiao, Chou Shu-Lei, Liu Hua-Kun, Wang Guoxiu, Dou Shi-Xue
Institute for Superconducting & Electronic Materials, University of Wollongong, Innovation Campus, Wollongong, NSW 2500, Australia.
Institute of Powder and New Energy Material Preparation Technology, Faculty of Metallurgical and Energy Engineering, Kunming University of Science and Technology, Kunming, 650093, China.
Angew Chem Int Ed Engl. 2022 Apr 11;61(16):e202200384. doi: 10.1002/anie.202200384. Epub 2022 Feb 21.
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 CoS electron reservoir enables the straight reduction of S to short-chain sodium polysulfides (Na S ) 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 at 5 A g with a high cycling capacity retention of 80 % after 5000 cycles at 5 A g .
动态调节硫活性对于实现高效稳定的室温钠硫(RT/Na-S)电池至关重要。在此,我们报道使用硫化钴作为电子储存库来提高硫阴极的活性,并同时与钴单原子结合作为双端结合位点以实现稳定的硫转化过程。合理构建的CoS电子储存库能够通过电子转移的简化氧化还原路径将硫直接还原为短链多硫化钠(Na S )。同时,钴单原子与电子储存库协同作用以加强简化的氧化还原路径,该路径固定原位形成的长链产物并催化其转化,从而实现高硫利用率和可持续的循环稳定性。所开发的硫阴极在5 A g 时表现出443 mAh g 的优异倍率性能,在5 A g 下5000次循环后具有80%的高循环容量保持率。