4.6 Article

Cooperative catalytic platinum species accelerating polysulfide redox reactions for Li-S batteries

期刊

JOURNAL OF ENERGY CHEMISTRY
卷 87, 期 -, 页码 123-135

出版社

ELSEVIER
DOI: 10.1016/j.jechem.2023.08.015

关键词

Lithium-sulfur batteries; Platinum species; N -doped carbon spheres; Bidirectional catalysis; Polysulfide conversion

向作者/读者索取更多资源

This study construct Pt nanoparticle loaded nitrogen-doped carbon spheres (Pt/NCS composites) as cathode materials to catalyze the dissociation/nucleation processes of Li2S in lithium-sulfur batteries. The active Pt0 and Pt2+ species are identified for accelerating the dissociation and nucleation of Li2S, respectively. In addition, bidirectional catalysis of active Pt species leads to the expedited conversion of sulfur species and improved redox kinetics. Therefore, Pt/NCS cathode exhibits enhanced long-term cyclability and rate capability.
The shuttle effect derived from diffusion of lithium polysulfides (LiPSs) and sluggish redox kinetic bring about poor cycling stability and low utilization of sulfur, which have always been the key challenging issues for the commercial application of lithium-sulfur (Li-S) batteries. Rational design of cathode materials to catalyze Li2S dissociation/nucleation processes is an appealing and valid strategy to develop high-energy practical Li-S batteries. Herein, considering the synergistic effect of bidirectional catalysis on LiPSs conversion and enhanced chemical immobilization for LiPSs by heteroatom doping, Pt nanoparticles loaded on nitrogen-doped carbon spheres (Pt/NCS composites) were constructed as cathode materials. According to the dynamic evolution of Pt catalysts and sulfur species, Pt0 and Pt2+ species were identified as active species for the accelerated dissociation and nucleation of Li2S, respectively. Meanwhile, in-situ Raman results demonstrated the expedited conversion of sulfur species resulted from bidirectional catalysis of active Pt species, corresponding to boosted redox kinetics. Consequently, Pt/NCS cathode exhibited improved long-term cyclability with high initial capacity, along with enhanced rate capability. This work provides a facile approach to construct cathode materials with bidirectional catalysis on Li2S dissociation/ nucleation, and sheds light on a more global understanding of the catalytic mechanism of metal catalysts during LiPSs conversion.(c) 2023 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据