多硫化物
化学工程
材料科学
碳纤维
催化作用
硫黄
电化学
锂(药物)
阴极
钼
热解
纳米技术
化学
有机化学
电极
复合材料
复合数
物理化学
冶金
内分泌学
工程类
医学
电解质
作者
Shungui Deng,Xiaotang Shi,Yüe Zhao,Chao Wang,Jinghua Wu,Xiayin Yao
标识
DOI:10.1016/j.cej.2021.133683
摘要
Lithium sulfur (Li-S) batteries hold promise as next-generation high energy density devices due to their high theoretical capacities. However, their commercialization confronts great challenges, in particular the notorious shuttle effect and sluggish kinetics, making it difficult to realize high sulfur loading and cell energy density properties. Herein, we explore the potential of molybdenum carbide (Mo2C) as the cathode catalyst to promote the polysulfide conversion. Nanosized Mo2C embedded porous carbon network (Mo2[email protected]) are prepared through the pyrolysis of molybdenum and chitosan precursor. Both electrochemical performance and theoretical calculations reveal that introducing the Mo2C can not only enhance the affinity toward the polysulfide intermediate, but also significantly accelerate the polysulfide interconversion compared with that of the pristine porous carbon network (PCN), thereby endowing the Li-S batteries with excellent cycling stability with a low capacity decay of 0.034 % per cycle over 600 cycles, and superb rate capability of 644 mAh g−1 at 5 A g−1.
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