多硫化物
杂原子
硫黄
石墨烯
动力学
电催化剂
活化能
电化学
化学
无机化学
催化作用
材料科学
化学工程
纳米技术
电极
有机化学
电解质
物理化学
工程类
物理
量子力学
戒指(化学)
作者
Lele Peng,Ziyang Wei,Chengzhang Wan,Jing Li,Zhuo Chen,Dan Zhu,Daniel Baumann,Haotian Liu,Christopher S. Allen,Xiang Xu,Angus I. Kirkland,Imran Shakir,Zeyad Almutairi,Sarah H. Tolbert,Bruce Dunn,Yu Huang,Philippe Sautet,Xiangfeng Duan
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2020-08-31
卷期号:3 (9): 762-770
被引量:555
标识
DOI:10.1038/s41929-020-0498-x
摘要
The fundamental kinetics of the electrocatalytic sulfur reduction reaction (SRR), a complex 16-electron conversion process in lithium–sulfur batteries, is so far insufficiently explored. Here, by directly profiling the activation energies in the multistep SRR, we reveal that the initial reduction of sulfur to the soluble polysulfides is relatively easy owing to the low activation energy, whereas the subsequent conversion of the polysulfides into the insoluble Li2S2/Li2S has a much higher activation energy, contributing to the accumulation of polysulfides and exacerbating the polysulfide shuttling effect. We use heteroatom-doped graphene as a model system to explore electrocatalytic SRR. We show that nitrogen and sulfur dual-doped graphene considerably reduces the activation energy to improve SRR kinetics. Density functional calculations confirm that the doping tunes the p-band centre of the active carbons for an optimal adsorption strength of intermediates and electroactivity. This study establishes electrocatalysis as a promising pathway to tackle the fundamental challenges facing lithium–sulfur batteries. The fundamental kinetics of the electrocatalytic sulfur reduction reaction, a complex 16-electron conversion process in lithium–sulfur batteries, is a topic that remains largely unexplored. Here, by directly profiling the activation energies in the multi-step reaction, the authors establish how the conversion kinetics differ for each step.
科研通智能强力驱动
Strongly Powered by AbleSci AI