"Atomic Topping" of MnOx on Al2O3 to Create Electron-Rich, Aperiodic, Lattice Oxygens that Resemble Noble Metals for Catalytic Oxidation

Enhancing the catalytic oxidation activity of traditional transition-metal oxides to rival that of noble metals has been a prominent focus in the field of catalysis. However, existing synthesis strategies that focus on controlling the electronic states of metal centers have not yet fully succeeded i...

Full description

Saved in:
Bibliographic Details
Published in:Journal of the American Chemical Society 2024-06, Vol.146 (24 p.16549-16557), p.16549-16557
Main Authors: Gan, Tao, Chen, Xin, Chu, Xuefeng, Jing, Pei, Shi, Shaozhen, Zhang, Zedong, Zhang, Wenxiang, Li, Jiong, Zhang, Shuo, Pavanello, Michele, Wang, Dayang, Liu, Gang
Format: Article
Language:English
Subjects:
absorption
adsorption
catalysts
catalytic activity
Fourier transform infrared spectroscopy
oxidation
oxygen
reaction kinetics
transmission electron microscopy
X-radiation
X-ray photoelectron spectroscopy
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Enhancing the catalytic oxidation activity of traditional transition-metal oxides to rival that of noble metals has been a prominent focus in the field of catalysis. However, existing synthesis strategies that focus on controlling the electronic states of metal centers have not yet fully succeeded in achieving this goal. Our current research reveals that manipulating the electronic states of oxygen centers can yield unexpected results. By creating electron-rich, aperiodic lattice oxygens through atomic topping of MnOx, we have produced a catalyst with performance that closely resembles supported Pt. Spherical aberration-corrected transmission electron microscopy and X-ray absorption spectra have confirmed that the atomic topping of the MnOx layer on Al2O3 can form an aperiodic arrangement oxide structure. Near-ambient pressure X-ray photoelectron spectroscopy, in situ diffuse reflectance infrared Fourier transform spectroscopy, reaction kinetics test, and theoretical calculations demonstrated that this structure significantly increases the electron density around the oxygen in MnOx, shifting the activation center for CO adsorption from Mn to O, thereby exhibiting catalytic activity and stability close to that of the precious metal Pt. This study presents a fresh perspective on designing efficient oxide catalysts by targeting electron-rich anionic centers, thereby deepening the understanding of how these centers can be altered to enhance catalytic efficiency in oxidation reactions.
ISSN:1520-5126
1520-5126
DOI:10.1021/jacs.4c03299