多硫化物
催化作用
硫黄
钴
电化学
化学
分离器(采油)
氧化还原
涂层
化学工程
无机化学
材料科学
纳米技术
电极
物理化学
有机化学
电解质
物理
工程类
热力学
作者
Ziwei Wang,Yuwen Cheng,Shan-Ying Wang,Jie Xu,Bo Peng,Dan Luo,Lianbo Ma
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-03-13
卷期号:16 (7): 9335-9343
被引量:42
标识
DOI:10.1007/s12274-023-5557-6
摘要
Although promising strategies have been developed to resolve the critical drawbacks of lithium-sulfur (Li-S) batteries, the intractable issues including undesirable shuttling of polysulfides and sluggish redox reaction kinetics have still been unresolved thoroughly. Herein, a cobalt single-atom (CoSA) catalyst comprising of atomic Co distributed homogeneously within nitrogen (N)-doped porous carbon (Co-NPC) nanosphere is constructed and utilized as a separator coating in Li-S batteries. The Co-NPC exposes abundant active sites participating in sulfur redox reactions, and remarkable catalytic activity boosting the rapid polysulfide conversions. As a result, Li-S batteries with Co-NPC coating layer realize significantly enhanced specific capacity (1295 mAh·g−1 at 0.2 C), rate capability (753 mAh·g−1 at 3.0 C), and long-life cyclic stability (601 mAh·g−1 after 500 cycles at 1.0 C). Increasing the areal sulfur loading to 6.2 mg·cm−2, an extremely high areal capacity of 7.92 mAh·cm−2 is achieved. Further in situ X-ray diffraction, density functional theory calculations, and secondary ion mass spectrometry confirm the high catalytic capability of CoSA towards reversible polysulfide conversion. This study supplies new insights for adopting single-atom catalyst to upgrade the electrochemical performance of Li-S batteries.
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