Related Experiment Video
Updated: Sep 17, 2026

Growth and Electrostatic/chemical Properties of Metal/LaAlO3/SrTiO3 Heterostructures
Published on: February 8, 2018
Lattice Strain and Charge Transfer Induced by the Ru@RuO2 Core-Shell Heterostructure Enable Efficient and Durable
Yuxiang Song1, Wanghui Zhao1, Weili Shi1
1Center of Artificial Photosynthesis for Solar Fuels and Department of Chemistry, School of Science and Research Center for Industries of the Future, Westlake University, Hangzhou, China.
Abstract:
Ru-based electrocatalysts are promising for low-cost proton exchange membrane (PEM) electrolyzers, but their stability is severely limited by the overoxidation of Ru sites during the acidic oxygen evolution reaction (OER). Herein, we propose a synthetic approach to convert the typical Ru/RuO2 heterostructure into a well-defined Ru@RuO2 core-shell structure, with preferential exposure of the (020) plane of RuO2. Such a core-shell design not only shields the metallic Ru core from direct contact with the oxidative catalytic environment, thereby suppressing metallic Ru overoxidation, but also maximizes the surface with abundant active sites on the (020) plane, leading to enhanced durability and intrinsic activity. Ru@RuO2 achieves a low overpotential of 165 mV at 10 mA·cm-2 and operates stably for over 1500 h. In a PEM electrolyzer, it delivers a current density of 1.0 A·cm-2 at 1.606 V and maintains stable operation for more than 200 h at 500 mA·cm-2. This study highlights metal-oxide core-shell heterostructures as a new paradigm for designing highly active and stable RuO2-based catalysts for acidic OER.
Related Concept Videos
Redox Equilibria: Overview
Electrochemical Cells
Ladder Diagrams: Redox Equilibria
Consider the Fe3+/Fe2+ half-reaction, which has a standard-state potential of +0.771 V. At potentials more positive than +0.771 V, Fe3+ predominates, whereas Fe2+...
Oxidation-Reduction Reactions
Electrochemical Systems
Heterogeneous Catalysis
