Facilitating the Construction of Strong Metal‐Support Interaction via Accelerating the Hydrogen Catalysis

W Wei Guo G Guoqiang Zhao (Institute of Science and Technology for New Energy) M Mingxia Gao H Hongge Pan (Institute of Science and Technology for New Energy) W Wenping Sun

Abstract

Abstract Strong metal‐support interaction (SMSI) critically regulates the catalytic performance of supported metal catalysts. Conventionally, a high‐temperature reduction (HTR) in H 2 is required to construct this state, a process that involves H 2 dissociation, spillover, and support activation. However, while a high temperature is indispensable to initiate SMSI, it also risks sintering the metal species, presenting a fundamental dilemma. Here, we demonstrate that this challenge can be overcome by accelerating the hydrogen catalysis kinetics through strategically manipulating active metal sites. As a proof of concept, by introducing Pt single atoms, the HTR temperature required to construct SMSI between Ru nanoparticles and TiO 2 is reduced from 600 to 400 °C. The key is that the Pt sites substantially promote the hydrogen spillover from Ru to TiO 2 , which is inherently sluggish due to an over‐strong Ru–H interaction. Both experimental and theoretical results confirm the accelerated support activation with the presence of Pt. The general effectiveness of this strategy is further validated by promoting SMSI formation in a Pd/TiO 2 system. The results highlight the significant role catalysis plays in SMSI manipulation and provide deeper insights into the SMSI formation mechanism, which is vital to the advancement of supported metal catalysts and beyond.

Article Details

Volume / Issue Vol. 65, Issue 5
Published January 28, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (5)

W

Wei Guo

G

Guoqiang Zhao

Institute of Science and Technology for New Energy

M

Mingxia Gao

H

Hongge Pan

Institute of Science and Technology for New Energy

W

Wenping Sun