Electrocatalytic Oxygen Reduction Using Metastable Zirconium Suboxide

Author:

Hu Huashuai1,Xu Zhihang2,Zhang Zhaorui1,Yan Xiaohui1,Zhu Ye2,Attfield J. Paul3,Yang Minghui1ORCID

Affiliation:

1. School of Environmental Science and Technology Dalian University of Technology No.2 Linggong Road, Ganjingzi District Dalian 116024 China

2. Department of Applied Physics, Research Institute for Smart Energy The Hong Kong Polytechnic University Hung Hom, Kowloon Hong Kong 999077 China

3. Centre for Science at Extreme Conditions and School of Chemistry University of Edinburgh King's Buildings, Mayfield Road Edinburgh EH9 3JZ UK

Abstract

AbstractStrategies for discovery of high‐performance electrocatalysts are important to advance clean energy technologies. Metastable phases such as low temperature or interfacial structures that are difficult to access in bulk may offer such catalytically active surfaces. We report here that the suboxide Zr3O, which is formed at Zr−ZrO2 interfaces but does not appear in the experimental Zr−O phase diagram exhibits outstanding oxygen reduction reaction (ORR) performance surpassing that of benchmark Pt/C and most transition metal‐based catalysts. Addition of Fe3C nanoparticles to give a Zr−Zr3O−Fe3C/NC catalyst (NC=nitrogen‐doped carbon) gives a half‐wave potential (E1/2) of 0.914 V, outperforming Pt/C and showing only a 3 mV decrease after 20,000 electrochemical cycles. A zinc‐air battery (ZAB) using this cathode material has a high power density of 241.1 mW cm−2 and remains stable for over 50 days of continuous cycling, demonstrating potential for practical applications. Zr3O demonstrates that interfacial or other phases that are difficult to stabilize may offer new directions for the discovery of high‐performance electrocatalysts.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Hong Kong Polytechnic University

Publisher

Wiley

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