Density-functional theory models of Fe(iv)O reactivity in metal–organic frameworks: self-interaction error, spin delocalisation and the role of hybrid exchange. Issue 22 (29th May 2020)

• Record Type: Journal Article
• Authors: Saiz, Fernan; Bernasconi, Leonardo
• Is Part Of: Physical chemistry chemical physics. Volume 22:Issue 22(2020)
• Page Start: 12821
• Page End: 12830
• Publication Date: 2020-05-29
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/d0cp01285h
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : We study the reactivity of Fe(iv )O moieties supported by a metal–organic framework (MOF-74) in the oxidation reaction of methane to methanol using all-electron, periodic density-functional theory calculations. Abstract : We study the reactivity of Fe(iv )O moieties supported by a metal–organic framework (MOF-74) in the oxidation reaction of methane to methanol using all-electron, periodic density-functional theory calculations. We compare results concerning the electronic properties and reactivity obtained using two hybrid (B3LYP and sc-BLYP) and two standard generalised gradient corrected (PBE and BLYP) semi-local density functional approximations. The semi-local functionals are unable to reproduce the expected reaction profiles and yield a qualitatively incorrect representation of the reactivity. Non-local hybrid functionals provide a substantially more reliable description and predict relatively modest ( ca. 60 kJ mol −1 ) reaction energy barriers for the H-atom abstraction reaction from CH4 molecules. We examine the origin of these differences and we highlight potential means to overcome the limitations of standard semi-local functionals in reactivity calculations in solid-state systems.