Mars–van Krevelen mechanism for CO oxidation on the polyoxometalates-supported Rh single-atom catalysts: An insight from density functional theory calculations

• Published in: Molecular catalysis Vol. 512; p. 111761
• Main Authors: Lin, Chun-Hong, Sun, Zi-Yi, Liu, Chun-Guang
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.08.2021
• Subjects: CO oxidation; Density functional theory; Mar-van Krevelen mechanism; Polyoxometalates; Single–atom catalysts; Density functional theory; Polyoxometalates; CO oxidation; Mar-van Krevelen mechanism; Single–atom catalysts
• ISSN: 2468-8231; 2468-8231
• DOI: 10.1016/j.mcat.2021.111761

•The mechanism of CO oxidation by O2 was studied over two POM-supported SACs (Rh1/PTA and Rh1/PMA).•The oxidation process involves consecutive oxidation of three CO molecules via a Rh-assisted MvK mechanism.•The second CO molecule was oxidized by the corner O atom of the POM support rather than adsorbed O2 molecule.•Oxidation state of the Rh center changes among III, II, and I, which promotes electron transfer and the whole reaction. The low and insufficient anchored site on support structure is the bottleneck problem for development of single-atom catalysts (SACs). Owing to the discrete anionic structure, the surface structure of unimolecular polyoxometalates (POMs) in solid is more like the fragments of metal oxide and possesses the unique separate structure, which can be viewed as the separate small “island” and effectively prevent agglomeration of single metal atoms. In the present paper, the mechanism of CO oxidation by O2 was systematically studied over two POM-supported SACs, Rh1/PTA and Rh1/PMA (PTA = [PW12O40]3− and PMA = [PMo12O40]3−) by means of density functional theory (DFT) calculations. The results indicated that this process involves consecutive oxidation of three CO molecules over Rh1/PTA and Rh1/PMA SACs via a Rh-assisted Mar-van Krevelen (MvK) mechanism. The first CO molecule was oxidized by a bridged O atom of POM support to form CO2 molecule and an oxygen vacancy. The surface oxygen vacancy was refilled by O2 molecule, and the second CO molecule was oxidized by a corner O atom of the POM support to form CO2 molecule and a new oxygen vacancy. Finally, the forming surface oxygen vacancy was replenished by the O2 molecule to form the key Mo-O-O-Mo unit, which can easily oxidize the third CO to form the CO2 molecule. Compared with the reported MvK mechanism, the significant difference arises from oxidation of the second CO molecule, in which the second CO molecule was oxidized by the corner O atom of the POM support rather than adsorbed O2 molecule. This is mainly due to a low reactivity for the adsorbed O2 molecule, which comes from a bonding interaction between the adsorbed O2 molecule and the single Rh atom. The atomic charge analysis show that the single Rh atom stabilized on the POM supports promotes the whole catalytic cycle via the change of oxidation state among III, II, and I. All these results show that the presence of single Rh atom on the unimolecular PTA and PMA supports is a key factor for determination of new reaction pathway and high reactivity. We hope our computation results can provide new physical insights to design SACs for CO oxidation by using unimolecular POM cluster. The reaction mechanism of CO oxidation by O2 was systematically studied over two polyoxometalate-supported single-atom catalysts by means of density functional theory calculations. [Display omitted]