Structurally‐Distorted RuIr‐Based Nanoframes for Long‐Duration Oxygen Evolution Catalysis

Author:

Liu Shangheng1,Tan Huang23,Huang Yu‐Cheng4,Zhang Qiaobao5,Lin Haiping3,Li Ling6,Hu Zhiwei7,Huang Wei‐Hsiang8,Pao Chih‐Wen8,Lee Jyh‐Fu8,Kong Qingyu9,Shao Qi6,Xu Yong2,Huang Xiaoqing1ORCID

Affiliation:

1. State Key Laboratory of Physical Chemistry of Solid Surfaces College of Chemistry and Chemical Engineering Xiamen University Xiamen 361005 China

2. Guangzhou Key Laboratory of Low‐Dimensional Materials and Energy Storage Devices Collaborative Innovation Center of Advanced Energy Materials School of Materials and Energy Guangdong University of Technology Guangzhou 510006 China

3. School of Physics and Information Technology Shaanxi Normal University Xi'an 710119 China

4. Department of Electrophysics National Yang Ming Chiao Tung University Hsinchu 30010 Taiwan

5. Department of Materials Science and Engineering College of Materials Xiamen University Xiamen 361005 China

6. College of Chemistry, Chemical Engineering and Materials Science Soochow University Jiangsu 215123 China

7. Max Planck Institute for Chemical Physics of Solids Nothnitzer Strasse 40 01187 Dresden Germany

8. National Synchrotron Radiation Research Center 101 Hsin‐Ann Road Hsinchu 30076 Taiwan

9. Synchrotron Soleil L'Orme des Merisiers St‐Aubin Gif‐sur‐Yvette Cedex 91192 France

Abstract

AbstractOxygen evolution reaction (OER) plays a key role in proton exchange membrane water electrolysis (PEMWE), yet the electrocatalysts still suffer from the disadvantages of low activity and poor stability in acidic conditions. Here, a new class of CdRu2IrOx nanoframes with distorted structure for acidic OER is successfully fabricated. Impressively, CdRu2IrOx displays an ultralow overpotential of 189 mV and an ultralong stability of 1500 h at 10 mA cm⁻2 toward OER in 0.5 M H2SO4. Moreover, a PEMWE using the distorted CdRu2IrOx can be steadily operated at 0.1 A cm⁻2 for 90 h. Microstructural analyses and X‐ray absorption spectroscopy (XAS) demonstrate that the synergy between Ru and Ir in CdRu2IrOx induces the distortion of Ru−O, Ir−O, and Ru−M (M = Ru, Ir) bonds. In situ XAS indicates that the applied potential leads to the deformation octahedral structure of RuOx/IrOx and the formation of stable Ru5+ species for OER. Theoretical calculations also reveal that the distorted structures can reduce the energy barrier of rate‐limiting step during OER. This work provides an efficient strategy for constructing structural distortion to achieve significant enhancement on the activity and stability of OER catalysts.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Priority Academic Program Development of Jiangsu Higher Education Institutions

Xiamen University

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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