多硫化物
X射线光电子能谱
材料科学
锂(药物)
催化作用
拉曼光谱
硫黄
电化学
硒化物
化学工程
过渡金属
成核
相(物质)
无机化学
化学
电极
物理化学
有机化学
电解质
冶金
内分泌学
工程类
硒
物理
光学
医学
作者
Ruilong Li,Zhe Bai,Wensuo Hou,Zeyu Wu,Pingli Feng,Yu Bai,Kening Sun,Zhenhua Wang
标识
DOI:10.1016/j.cclet.2023.108263
摘要
The sluggish conversion kinetics and shuttle effect of lithium polysulfides (LiPSs) severely hamper the commercialization of lithium–sulfur batteries. Numerous electrocatalysts have been used to address these issues, amongst which, transition metal dichalcogenides have shown excellent catalytic performance in the study of lithium–sulfur batteries. Note that dichalcogenides in different phases have different catalytic properties, and such catalytic materials in different phases have a prominent impact on the performance of lithium–sulfur batteries. Herein, 1T-phase rich MoSe2 (T-MoSe2) nanosheets are synthesized and used to catalyze the conversion of LiPSs. Compared with the 2H-phase rich MoSe2 (H-MoSe2) nanosheets, the T-MoSe2 nanosheets significantly accelerate the liquid phase transformation of LiPSs and the nucleation process of Li2S. In-situ Raman and X-ray photoelectron spectroscopy (XPS) find that T-MoSe2 effectively captures LiPSs through the formation of Mo-S and Li-Se bonds, and simultaneously achieves fast catalytic conversion of LiPSs. The lithium–sulfur batteries with T-MoSe2 functionalized separators display a fantastic rate performance of 770.1 mAh/g at 3 C and wonderful cycling stability, with a capacity decay rate as low as 0.065% during 400 cycles at 1 C. This work offers a novel perspective for the rational design of selenide electrocatalysts in lithium–sulfur chemistry.
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