Methane Activation by [AlFeO3]+: the Hidden Spin Selectivity

Author:

Yan Linghui12,Yuan BoWei12,Qian Chao12,Zhou Shaodong12ORCID

Affiliation:

1. College of Chemical and Biological Engineering Zhejiang Provincial Key Laboratory of Advanced Chemical Engineering Manufacture Technology Zhejiang University 310027 Hangzhou P. R. China

2. Institute of Zhejiang University - Quzhou Zheda Rd. #99 324000 Quzhou P.R. China

Abstract

AbstractThe performance of heteronuclear cluster [AlFeO3]+ in activating methane has been explored by a combination of high‐level quantum chemical calculations with gas‐phase experiments. At room temperature, [AlFeO3]+ is a mixture of 7[AlFeO3]+ and 5[AlFeO3]+, in which two states lead to different reactivity and chemoselectivity for methane activation. While hydrogen extracted from methane is the only product channel for the 7[AlFeO3]+/CH4 couple, 5[AlFeO3]+ is able to convert this substrate to formaldehyde. In addition, the introduction of an external electric field may regulate the reactivity and product selectivity. The interesting doping effect of Fe and the associated electronic origins are discussed, which may guide one on the design of Fe‐involved catalyst for methane conversion.

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,Atomic and Molecular Physics, and Optics

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