硫化钴
电化学
硫黄
化学工程
材料科学
碳纳米纤维
氧化还原
电化学动力学
电极
成核
碳纤维
钴
静电纺丝
纳米纤维
催化作用
无机化学
复合数
化学
纳米技术
碳纳米管
复合材料
有机化学
物理化学
工程类
冶金
聚合物
作者
Shanshan Yao,Cuijuan Zhang,Ruiduo Guo,Arslan Majeed,Yanping He,Youqiang Wang,Xiangqian Shen,Tianbao Li,Shibiao Qin
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2020-08-17
卷期号:8 (36): 13600-13609
被引量:72
标识
DOI:10.1021/acssuschemeng.0c02869
摘要
Lithium sulfur (Li–S) batteries have been considerably studied in energy storage systems because of their extremely high energy density. Nevertheless, poor sulfur utilization and lower sulfur loading, polysulfides shuttling, and short cycling life are the major obstacles to their application. Herein, we present the cubic structure of CoS2 microcrystals decorated on Co/N-codoped carbon nanofibers (denoted as CSCNC) by an electrospinning technique followed by a hydrothermal process. The Li2S6 catholyte was added in the fibrous CSCNC network as the current free electrode for Li–S batteries, which was used as the positive catalyst to restrain the shuttle effect and facilitate the reaction kinetics. Additionally, CoS2 and Co are dual functional electrocatalysts for facilitating lithium sulfide nucleation onto the surface of CSCNC, thus reduce electrochemical polarization and enhance the specific capacity. This CSCNC@Li2S6 electrode exhibits 877 mAh g–1 capacity retention with sulfur loading of 7.11 mg over 200 cycles and has an average decay of 0.11% per cycle. Additionally, the composite electrode with sulfur loading accomplishes up to 14.22 mg, providing 12.7 mAh of extremely high capacity, which is much higher than that of the carbon-based electrodes for Li–S batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI