Recent Progress of Transition Metal Selenides for Electrochemical Oxygen Reduction to Hydrogen Peroxide: From Catalyst Design to Electrolyzers Application

Author:

Wang Yingnan1,Han Caidi1,Ma Li2,Duan Tigang2,Du Yue1,Wu Jinting1,Zou Ji‐Jun3ORCID,Gao Jian1,Zhu Xiao‐Dong1,Zhang Yong‐Chao1ORCID

Affiliation:

1. State Key Laboratory Base of Eco‐Chemical Engineering College of Chemical Engineering Qingdao University of Science & Technology Qingdao 266042 China

2. State Key Laboratory for Marine Corrosion and Protection Luoyang Ship Material Research Institute Qingdao 266237 China

3. Key Laboratory for Green Chemical Technology of Ministry of Education School of Chemical Engineering and Technology Tianjin University Tianjin 300072 China

Abstract

AbstractHydrogen peroxide (H2O2) is a highly value‐added and environmental‐friendly chemical with various applications. The production of H2O2 by electrocatalytic 2e oxygen reduction reaction (ORR) has emerged as a promising alternative to the energy‐intensive anthraquinone process. High selectivity Catalysts combining with superior activity are critical for the efficient electrosynthesis of H2O2. Earth‐abundant transition metal selenides (TMSs) being discovered as a classic of stable, low‐cost, highly active and selective catalysts for electrochemical 2e ORR. These features come from the relatively large atomic radius of selenium element, the metal‐like properties and the abundant reserves. Moreover, compared with the advanced noble metal or single‐atom catalysts, the kinetic current density of TMSs for H2O2 generation is higher in acidic solution, which enable them to become suitable catalyst candidates. Herein, the recent progress of TMSs for ORR to H2O2 is systematically reviewed. The effects of TMSs electrocatalysts on the activity, selectivity and stability of ORR to H2O2 are summarized. It is intended to provide an insight from catalyst design and corresponding reaction mechanisms to the device setup, and to discuss the relationship between structure and activity.

Funder

Natural Science Foundation of Shandong Province

China Postdoctoral Science Foundation

Publisher

Wiley

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