多硫化物
法拉第效率
硫化物
纳米颗粒
氧化还原
催化作用
材料科学
X射线光电子能谱
硫黄
锂硫电池
化学工程
无机化学
电化学
纳米技术
化学
电极
有机化学
电解质
冶金
物理化学
工程类
作者
Monica J. Theibault,Connor R. McCormick,Shuang‐Yan Lang,Raymond E. Schaak,Héctor D. Abruña
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-09-17
卷期号:17 (18): 18402-18410
被引量:36
标识
DOI:10.1021/acsnano.3c05869
摘要
The polysulfide shuttle contributes to capacity loss in lithium–sulfur batteries, which limits their practical utilization. Materials that catalyze the complex redox reactions responsible for the polysulfide shuttle are emerging, but foundational knowledge that enables catalyst development remains limited with only a small number of catalysts identified. Here, we employ a rigorous electrochemical approach to show quantitatively that the lithium polysulfide redox reaction is catalyzed by nanoparticles of a high entropy sulfide material, Zn0.30Co0.31Cu0.19In0.13Ga0.06S. When 2% by weight of the high entropy sulfide is added to the lithium sulfur cathode composite, the capacity and Coulombic efficiency of the resulting battery are improved at both moderate (0.2 C) and high (1 C) charge/discharge rates. Surface analysis of the high entropy sulfide nanoparticles using X-ray photoelectron spectroscopy provides important insights into how the material evolves during the cycling process. The Zn0.30Co0.31Cu0.19In0.13Ga0.06S nanoparticle catalyst outperformed the constituent metal sulfides, pointing to the role that the high-entropy "cocktail effect" can play in the development of advanced electrocatalytic materials for improved lithium sulfur battery performance.
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