Chemical Research in Chinese Universities ›› 2026, Vol. 42 ›› Issue (3): 805-812.doi: 10.1007/s40242-026-5252-8

• Research Articles • Previous Articles     Next Articles

Accelerating Electron Transfer via Ternary Heterostructures for Enhanced Acidic Oxygen Evolution Performance

YANG Peizhi1, DENG Liming1, WANG Luqi1, ZHAO Sheng1, LI Linlin1, PENG Shengjie2   

  1. 1. College of Materials Science and Technology, Nanjing University of Aeronautics and Astronautics, Nanjing, 210016, P. R. China;
    2. Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center, Southeast University, Nanjing, 211189, P. R. China
  • Received:2025-10-19 Accepted:2025-11-27 Published:2026-06-02
  • Contact: PENG Shengjie,E-mail:pengshengjie@seu.edu.cn E-mail:pengshengjie@seu.edu.cn
  • Supported by:
    This work was supported by the National Natural Science Foundation of China (Nos. 92472117, 22509085, and 52371226), the Natural Science Foundation of Jiangsu Province, China (Nos. BK20221482 and BK20210311), the China National Postdoctoral Program for Innovative Talents (No. BX20250441), the China Postdoctoral Science Foundation (No. 2025M774272), the Postgraduate Research & Practice Innovation Program of Nanjing University of Aeronautics and Astronautics, China (No. xcxjh20240602), and the Jiangsu Funding Program for Excellent Postdoctoral Talent, China.

Abstract: Developing ruthenium-based catalysts with high activity and long-term stability is crucial for sustaining efficient oxygen evolution reactions (OER) under acidic conditions. Here, we develop a ruthenium-titanium-tin oxide (RuO2/TiSnOx) electrocatalyst featuring a rationally engineered ternary heterostructure composed of RuO2, TiO2, and SnO2 phases with well-defined interfaces. Such a unique architecture establishes a multidirectional electron transport network, which accelerates electron delivery to Ru active sites and mitigates local charge accumulation, thereby suppressing overoxidation and dissolution of Ru under acidic conditions. Structural and spectroscopic characterizations confirm the formation of coherent heterointerfaces, which reconstruct the coordination environment of Ru, thereby favoring optimal adsorption of OER intermediates. Benefiting from synergistic effects, the RuO2/TiSnOx catalyst achieves a remarkably low overpotential of 187 mV at 10 mA/cm2 in 0.5 mol/L H2SO4 and maintains stable operation for 500 h, outperforming most previous Ru-based catalysts. This study demonstrates that ternary heterostructure engineering provides an effective pathway to balance activity and stability in Ru-based acidic OER catalysts, advancing the practical application in proton exchange membrane water electrolysis (PEMWE) systems for green hydrogen production.

Key words: Oxygen evolution reaction, Ternary heterostructure, Electronic environment modulation, Ru-based catalyst