多硫化物
铜
电化学
材料科学
硒化物
阴极
硫黄
锂(药物)
化学工程
化学吸附
相(物质)
无机化学
催化作用
电极
电解质
纳米技术
化学
物理化学
冶金
硒
有机化学
医学
工程类
内分泌学
作者
Dawei Yang,Mengyao Li,Xuejiao Zheng,Xu Han,Chaoqi Zhang,Jordi Jacas Biendicho,Jordi Llorca,Jiaao Wang,Hongchang Hao,Junshan Li,Graeme Henkelman,Jordi Arbiol,J.R. Morante,David Mitlin,Shulei Chou,Andreu Cabot
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-06-27
卷期号:16 (7): 11102-11114
被引量:73
标识
DOI:10.1021/acsnano.2c03788
摘要
The shuttling of soluble lithium polysulfides (LiPS) and the sluggish Li-S conversion kinetics are two main barriers toward the practical application of lithium-sulfur batteries (LSBs). Herein, we propose the addition of copper selenide nanoparticles at the cathode to trap LiPS and accelerate the Li-S reaction kinetics. Using both computational and experimental results, we demonstrate the crystal phase and concentration of copper vacancies to control the electronic structure of the copper selenide, its affinity toward LiPS chemisorption, and its electrical conductivity. The adjustment of the defect density also allows for tuning the electrochemically active sites for the catalytic conversion of polysulfide. The optimized S/Cu1.8Se cathode efficiently promotes and stabilizes the sulfur electrochemistry, thus improving significantly the LSB performance, including an outstanding cyclability over 1000 cycles at 3 C with a capacity fading rate of just 0.029% per cycle, a superb rate capability up to 5 C, and a high areal capacity of 6.07 mAh cm-2 under high sulfur loading. Overall, the present work proposes a crystal phase and defect engineering strategy toward fast and durable sulfur electrochemistry, demonstrating great potential in developing practical LSBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI