Balancing Adsorption, Catalysis, and Desorption in Cathode Catalyst For Li–S Batteries

Author:

Zhang Wei12,Pan Hui3,Han Ning1,Feng Shihui4,Zhang Xuan15ORCID,Guo Wei1,Tan Pingping5,Xie Sijie1,Zhou Zhenyu1,Ma Qianru1,Guo Xiaolong6,Vlad Alexandru6,Wübbenhorst Michael3,Luo Jiangshui2,Fransaer Jan1

Affiliation:

1. Department of Materials Engineering KU Leuven Leuven 3001 Belgium

2. Lab of Electrolytes and Phase Change Materials College of Materials Science and Engineering Sichuan University Chengdu 610065 P. R. China

3. Laboratory for Soft Matter and Biophysics Department of Physics and Astronomy KU Leuven Leuven 3001 Belgium

4. Department of Material and Environmental Chemistry Stockholm University Stockholm SE 106‐91 Sweden

5. ZJU‐Hangzhou Global Scientific and Technological Innovation Centre Zhejiang University Hangzhou 311200 P. R. China

6. Institute of Condensed Matter and Nanosciences Université Catholique de Louvain Louvain‐la‐Neuve 1348 Belgium

Abstract

AbstractThe complicated electrochemical catalytic conversion process of polysulfides in metal–sulfur batteries involves three steps: adsorption, catalysis, and desorption process. Even as huge efforts are made for the understanding of the separate steps (especially for the adsorption and catalysis process), research focusing on the entire process is still scarce. Herein, a series of cobalt phosphides (CoP, CoP2, and CoP3) is employed with identical hollow morphology as model electrocatalysts to investigate the significance of the desorption process and discuss the balancing among the adsorption, catalysis, and desorption of lithium polysulfides (LiPSs). The experimental data demonstrate that, compared to CoP and CoP3, CoP2 exhibits moderate adsorption of LiPSs, which enhances the reduction kinetics of S8 to Li2S and regulates the desorption of short‐chain LiPSs. Theoretical calculations further confirm that CoP2 with moderate adsorption of LiPSs exhibits better redox kinetics of LiPSs compared to CoP and CoP3. Moderate adsorption enables the CoP2‐based sulfur cathode to deliver excellent stability with 86% capacity retention (2.6 and 2.0 times higher than CoP and CoP3, respectively) over 1000 cycles at 1 C. All these results indicate that in the adsorption‐catalysis‐desorption chain for LiPSs, all steps need to be considered rather than just focusing on one step of the process.

Funder

Fonds Wetenschappelijk Onderzoek

National Natural Science Foundation of China

Sichuan Province Science and Technology Support Program

National Key Research and Development Program of China

Publisher

Wiley

Subject

General Materials Science,Renewable Energy, Sustainability and the Environment

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