Low‐Cost Self‐Reconstructed High Entropy Oxide as an Ultra‐Durable OER Electrocatalyst for Anion Exchange Membrane Water Electrolyzer

Author:

Karthikeyan S.C.1,Ramakrishnan Shanmugam2,Prabhakaran Sampath3,Subramaniam Mohan Raj14,Mamlouk Mohamed2,Kim Do Hwan15,Yoo Dong Jin16ORCID

Affiliation:

1. Department of Energy Storage/Conversion Engineering (BK21 FOUR) for Graduate School Hydrogen and Fuel Cell Research Center Jeonbuk National University Jeonju Jeollabuk‐do 54896 Republic of Korea

2. School of Engineering Newcastle University Newcastle upon Tyne NE1 7RU United Kingdom

3. Department of Nano Convergence Engineering Jeonbuk National University Jeonju Jeonbuk 54896 Republic of Korea

4. Department of Chemistry Centre for Research and Development KPR Institute of Engineering and Technology Coimbatore Tamilnadu 641 407 India

5. Division of Science Education Jeonbuk National University Jeonju Jeonbuk 54896 Republic of Korea

6. Department of Life Science Jeonbuk National University Jeonju Jeollabuk‐do 54896 Republic of Korea

Abstract

AbstractFuture energy loss can be minimized to a greater extent via developing highly active electrocatalysts for alkaline water electrolyzers. Incorporating an innovative design like high entropy oxides, dealloying, structural reconstruction, in situ activation can potentially reduce the energy barriers between practical and theoretical potentials. Here, a Fd‐3m spinel group high entropy oxide is developed via a simple solvothermal and calcination approach. The developed (FeCoMnZnMg)3O4 electrocatalyst shows a near equimolar distribution of all the metal elements resulting in higher entropy (ΔS ≈1.61R) and higher surface area. The self‐reconstructed spinel high entropy oxide (S‐HEO) catalyst exhibited a lower overpotential of 240 mV to reach 10 mA cm−2 and enhanced reaction kinetics (59 mV dec−1). Noticeably, the S‐HEO displayed an outstanding durability of 1000 h without any potential loss, significantly outperforming most of the reported OER electrocatalysts. Further, S‐HEO is evaluated as the anode catalyst for an anion exchange membrane water electrolyzer (AEMWE) in 1 m, 0.1 m KOH, and DI water at 20 and 60 °C. These results demonstrate that S‐HEO is a highly attractive, non‐noble class of materials for high active oxygen evolution reaction (OER) electrocatalysts allowing fine‐tuning beyond the limits of bi‐ or trimetallic oxides.

Funder

National Research Foundation of Korea

Ministry of Education

UK Research and Innovation

Publisher

Wiley

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