Strong Electronic Interaction of Amorphous Fe2O3 Nanosheets with Single-Atom Pt toward Enhanced Carbon Monoxide Oxidation

86Citations
Citations of this article
33Readers
Mendeley users who have this article in their library.

Abstract

Platinum-based catalysts are critical to several chemical processes, but their efficiency is not satisfying enough in some cases, because only the surface active-site atoms participate in the reaction. Henceforth, catalysts with single-atom dispersions are highly desirable to maximize their mass efficiency, but fabricating these structures using a controllable method is still challenging. Most previous studies have focused on crystalline materials. However, amorphous materials may have enhanced performance due to their distorted and isotropic nature with numerous defects. Here reported is the facile synthesis of an atomically dispersed catalyst that consists of single Pt atoms and amorphous Fe2O3 nanosheets. Rational control can regulate the morphology from single atom clusters to sub-nanoparticles. Density functional theory calculations show the synergistic effect resulted from the strong binding and stabilization of single Pt atoms with the strong metal-support interaction between the in situ locally anchored Pt atoms and Fe2O3 lead to a weak CO adsorption. Moreover, the distorted amorphous Fe2O3 with O vacancies is beneficial for the activation of O2, which further facilitates CO oxidation on nearby Pt sites or interface sites between Pt and Fe2O3, resulting in the extremely high performance for CO oxidation of the atomic catalyst.

Cite

CITATION STYLE

APA

Chen, W., Ma, Y., Li, F., Pan, L., Gao, W., Xiang, Q., … Wu, J. (2019). Strong Electronic Interaction of Amorphous Fe2O3 Nanosheets with Single-Atom Pt toward Enhanced Carbon Monoxide Oxidation. Advanced Functional Materials, 29(42). https://doi.org/10.1002/adfm.201904278

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free