Boosting polysulfide redox conversion of Li-S batteries by one-step-synthesized Co-Mo bimetallic nitride

多硫化物 双金属片 电化学 氮化物 X射线光电子能谱 催化作用 硫黄 法拉第效率 化学工程 化学 阴极 材料科学 电解质 电极 纳米技术 有机化学 物理化学 工程类 图层(电子)
作者
Yingying Yan,Hongtai Li,Chen Cheng,Tianran Yan,Wenping Gao,Jing Mao,Kehua Dai,Liang Zhang
出处
期刊:Journal of Energy Chemistry [Elsevier]
卷期号:61: 336-346 被引量:90
标识
DOI:10.1016/j.jechem.2021.03.041
摘要

Lithium-sulfur (Li-S) batteries are considered as one of the most promising next generation energy storage systems due to the high theoretical specific capacity, low cost, and environmental benignity. However, the notorious shuttle effect of polysulfides hinders the practical application of Li-S batteries. Herein, we have rationally designed and synthesized sea urchin-like Co-Mo bimetallic nitride (Co3Mo3N) in the absence of additional nitrogen sources with only one step, which was applied as the sulfur host materials for Li-S batteries. The results indicate that Co3Mo3N can efficiently anchor and catalyze the conversion of polysulfides, thus accelerating the electrochemical reaction kinetics and enabling prominent electrochemical properties. As a consequence, the [email protected]3Mo3N cathode exhibits a high rate performance of 705 mAh g−1 at 3 C rate and an excellent cycling stability with a low capacity fading rate of 0.08% per cycle at 1 C over 600 cycles. Even at a high sulfur loading of 5.4 cmg cm−2, it delivers a high initial areal capacity of 4.50 mAh cm−2, which is still retained at 3.64 mAh cm−2 after 120 cycles. Furthermore, the catalytic mechanism and structural stability of Co3Mo3N during cycling were elucidated by a combination of X-ray photoelectron spectroscopy and X-ray absorption fine structure. This work highlights the strategy of structure-catalysis engineering of bimetallic nitride, which is expected to have a wide application in Li-S batteries.
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