Embedded‐Type Cu Nanoparticle with Largely Enhanced Catalytic Activity and Stability Toward Methanol Steam Reforming

H Hao Meng T Tianyao Shen (State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing P. R. China) Z Zhiming Yin (State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing P. R. China) Y Yusen Yang (State Key Laboratory of Chemical Resource Engineering) J Jian Zhang K Kai Feng (Department of Chemical Engineering) S Shaoteng Yuan (State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing P. R. China) L Lei Wang E Enze Xu (State Key Laboratory of Chemical Resource Engineering, Beijing Advanced Innovation Center for Soft Matter Science and Engineering Beijing University of Chemical Technology Beijing 100029 P.R. China) L Lirong Zheng S Song Hong (State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing P. R. China) F Feng‐Shou Xiao (Key Lab of Biomass Chemical Engineering of Ministry of Education College of Chemical and Biological Engineering Zhejiang University Hangzhou 310027 China) M Min Wei (Department of Chemistry and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province)

Abstract

Abstract Hydrogen production through low‐temperature methanol steam reforming (MSR) reaction plays a critical role in the development of new energy but remains a great challenge. Herein, we report a Cu/Zn(Ga)O x catalyst, which is prepared via an interface reconstruction strategy. Interestingly, this catalyst is featured with a unique mortise‐and‐tenon structure: Cu nanoparticles are embedded into the Zn(Ga)O x substrate, which ensures a stable Zn–O–Cu + –O v –Ga δ + interface structure. The resulting Cu/Zn(Ga)O x catalyst exhibits 99.3% CH 3 OH conversion with an H 2 production rate of 124.6 µmol g cat −1  s −1 at 225 °C, which is preponderant to the state‐of‐the‐art catalysts. Furthermore, an ultra‐high catalytic stability was demonstrated through a 400 h stream‐on‐line test without obvious decline. Kinetic isotope analysis, in situ spectroscopy characterizations, and theoretical calculations reveal that the MSR reaction over Cu/Zn(Ga)O x catalyst follows the formaldehyde oxidation route. The CH 3 O* and H 2 O molecule adsorb at the adjacent Cu + −O v interface (intrinsic active site) with an oxygen‐terminal adsorption configuration, which promotes electron transfer from the d ‐band center of Cu to the O ( s , p )‐band of the substrate molecule. This significantly reduces the energy barrier of C─H bond cleavage in CH 3 O* dehydrogenation (the rate‐determining step) and H 2 O dissociation, accounting for the extraordinarily enhanced H 2 production.

Article Details

Volume / Issue Vol. 64, Issue 33
Published August 11, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (13)

H

Hao Meng

T

Tianyao Shen

State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing P. R. China

Z

Zhiming Yin

State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing P. R. China

Y

Yusen Yang

State Key Laboratory of Chemical Resource Engineering

J

Jian Zhang

K

Kai Feng

Department of Chemical Engineering

S

Shaoteng Yuan

State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing P. R. China

L

Lei Wang

E

Enze Xu

State Key Laboratory of Chemical Resource Engineering, Beijing Advanced Innovation Center for Soft Matter Science and Engineering Beijing University of Chemical Technology Beijing 100029 P.R. China

L

Lirong Zheng

S

Song Hong

State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing P. R. China

F

Feng‐Shou Xiao

Key Lab of Biomass Chemical Engineering of Ministry of Education College of Chemical and Biological Engineering Zhejiang University Hangzhou 310027 China

M

Min Wei

Department of Chemistry and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province