J. Mater. Sci. Technol. ›› 2026, Vol. 254: 71-80.DOI: 10.1016/j.jmst.2025.07.044

• Research Article • Previous Articles     Next Articles

Two-dimensional lamellar TiO2 surface-loaded RuCo nanoclusters for pH-universal electrocatalytic hydrogen evolution

Enhao Liua,1, Xiaochun Wanga,1, Jinzhou Lib, Chao Chena,*, Qian Lib,c, Xuewei Lvb, Jie Dangb,*   

  1. aCollege of Materials Science and Engineering, Taiyuan University of Technology, Taiyuan 030024, China;
    bCollege of Materials Science and Engineering, Chongqing University, Chongqing 400044, China;
    cState Key Laboratory of Advanced Special Steels &Shanghai Key Laboratory of Advanced Ferrometallurgy, School of Materials Science and Engineering, Shanghai University, Shanghai 200444, China
  • Received:2025-06-09 Revised:2025-07-26 Accepted:2025-07-30 Online:2026-05-08
  • Contact: *E-mail addresses: chenchao@tyut.edu.cn (C. Chen), jiedang@cqu.edu.cn (J. Dang)
  • About author:1These authors contributed equally to this work.

Abstract: The development of cost-effective, efficient, and corrosion-resistant electrocatalysts is crucial for industrial hydrogen production under universal pH conditions. In this study, RuCo nanoclusters were deposited onto Ti3C2Tx MXene using an impregnation method and subsequently annealed in a mildly oxidative atmosphere, leading to the formation of anatase TiO2 with retained 2D morphology. This transformation significantly improved the material’s oxidation and corrosion resistance. Furthermore, the spatial confinement effect of MXene ensured the uniform dispersion of RuCo nanoparticles on the catalyst surface after annealing, thereby exposing abundant active sites. The catalyst delivers low hydrogen evolution overpotentials of 44 mV in 1 M KOH and 50 mV in 0.5 M H2SO4 at a current density of 10 mA cm-2. Characterization and theoretical calculations indicate that Co doping donates additional electrons to Ru, stabilizing its low-valence state and thus improving the overall structural stability. This localized charge transfer further tunes the D-band center of Ru sites, promoting optimal interactions with reaction intermediates. As a result, it lowers the energy barrier and enhances the catalytic activity.

Key words: Lamellar TiO2, pH -universal, Hydrogen evolution reaction, Metal-support interactions, First-principles calculations