journal article·2024-11-04Open access

Cationic and Anionic Dual Redox Activity of MoS 2 for Electrochemical Potassium Storage

Ajay Piriya Vijaya Kumar Saroja, Yupei Han, Charlie A. F. Nason, Gopinathan Sankar, Pan He, Yi Lu, Henry R. Tinker, Andrew Stewart, Veronica Celorrio, Min Zhou, Jiayan Luo, Yang Xu

ACS Materials Letters· Volume 6· Issue 11

Abstract

High Resolution Image Download MS PowerPoint Slide MoS 2 is regarded as one of the most promising potassium-ion battery (PIB) anodes. Despite the great progress to enhance its electrochemical performance, understanding of the electrochemical mechanism to store K-ions in MoS 2 remains unclear. This work reports that the K storage process in MoS 2 follows a complex reaction pathway involving the conversion reactions of Mo and S, showing both cationic redox activity of Mo and anionic redox activity of S. The presence of dual redox activity, characterized in-depth through synchrotron X-ray absorption, X-ray photoelectron, Raman, and UV–vis spectroscopies, reveals that the irreversible Mo oxidation during the depotassiation process directs the reaction pathway toward S oxidation, which leads to the occurrence of K–S electrochemistry in the (de)potassiation process. Moreover, the dual reaction pathway can be adjusted by controlling the discharge depth at different cycling stages of MoS 2, realizing a long-term stable cycle life of MoS 2 as a PIB anode.
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Research context

OpenAlex topics: Advancements in Battery Materials · 2D Materials and Applications · Advanced battery technologies research

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Affiliations

Department of Chemistry

University College London

Diamond Light Source

Harwell Science and Innovation Campus

Hefei National Research Center for Physical Sciences at the Microscale, School of Chemistry and Materials Science

University of Science and Technology of China

State Key Laboratory of Metal Matrix Composites, School of Materials Science and Engineering

Shanghai Jiao Tong University

Funding

Engineering and Physical Sciences Research Council · Royal Society · Leverhulme Trust · Diamond Light Source

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