Chinese Journal of Catalysis ›› 2026, Vol. 89: 232-245.DOI: 10.1016/S1872-2067(26)65155-8

• Article • Previous Articles     Next Articles

Autogenous force-mediated assembly: A general strategy for constructing single-atom architectures in hierarchical hybrid electrocatalysts

Ting Lia, Xiaohui Chena, Xiaolin Lia, Qi Xiaob,*(), Hongqun Luoa,*(), Nianbing Lia,*()   

  1. aSchool of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China
    bSchool of Chemistry and Materials, Nanning Normal University, Nanning 530001, Guangxi, China
  • Received:2026-01-07 Accepted:2026-03-12 Online:2026-10-18 Published:2026-09-01
  • Contact: *E-mail:qi.xiao@nnnu.edu.cn(Q. Xiao),luohq@swu.edu.cn (H. Luo),linb@swu.edu.cn(N. Li).
  • Supported by:
    National Natural Science Foundation of China(21675131);Natural Science Foundation of Chongqing(cstc2020jcyj-zdxmX0003);Natural Science Foundation of Chongqing(CSTB2023NSCQ-MSX0924)

Abstract:

The design of efficient and pH-universal ruthenium (Ru) single-atom catalysts (SACs) remains a pivotal challenge for hydrogen economy systems. Here, inspired by tubular capillary phenomena, a novel approach is introduced—autogenous force-mediated assembly—enabled by a unique asymmetric N-doped carbon nanotubes (NCNTs) scaffold with a Co-embedded sealed end. The confined geometry drives a spontaneous, directional outward migration of Co2+ species at room temperature, which deposit as amorphous or poorly crystalline cobalt-based compounds at the outer surface while concurrently capturing and stabilizing Ru species in single-atom configurations. And these precursors transform into well-crystallized Co3O4 anchored with Ru single-atom upon calcination. This process yields a precisely organized three-dimensional architecture where metallic Co nanoparticles remain confined within the NCNTs, while atomically dispersed Ru sites are firmly anchored on the exterior Co3O4 lattice. The gradual migration-deposition process is inherently self-limiting, ensuring uniform dispersion of Ru single-atoms (SAs). The resulting lattice confinement induces a strong electronic metal-support interaction (EMSI), which effectively suppresses atomic aggregation and optimizes the electronic structure of the active sites. The integrated system—coupling the conductive Co@NCNT with the EMSI-enhanced Ru-Co3O4 interface—delivers outstanding hydrogen evolution reaction performance. This work establishes a generalizable synthesis paradigm that leverages internally generated forces for the precise spatial organization of active components, presenting a versatile route toward high-performance SACs for sustainable energy conversion.

Key words: Single-atom catalysts, Hydrogen evolution reaction, Metal-support interaction, Carbon nanotubes, Three-dimensional hierarchical, material