Author, as appears in the article.: López, J. ; Musaev, D. ; Craig, H. ; Galán-Mascarós, J. R. ; Carbó, J. ; Poblet, J. M:

Department: Química Física i Inorgànica

URV's Author/s: LÓPEZ FERNÁNDEZ, JAVIER; Musaev, D. ; Craig, H. ; Galán-Mascarós, J. R. ; CARBÓ MARTIN, JORGE JUAN; POBLET RIUS, JOSEP MARIA

Keywords: polyoxometalates water oxidation catalysis DFT

Abstract: A mechanism of water oxidation catalyzed by the carbon-free tetra-Co containing polyoxometalates [Co4(H2O)2(PW9O34)2]10− (PCo4) and [Co4(H2O)2(VW9O34)2]10− (VCo4) is elucidated by DFT calculations. Computational analysis for PCo4 suggests that a first PCET step may proceed via a sequential electron-then-proton transfer (ET + PT) pathway and leads to one electron oxidize species S1 (POM-CoIIIOH). In contrast, the second PCET, which controls the potential required to form POM-CoIII active species S2 is clearly a concerted process. The overall S0 → S2 transformation is estimated to require less than 1.48 V and 1.62 V applied potential at pH = 8 for PCo4 and VCo4 anions, respectively. At operando conditions, with the presence of a buffer and with an applied potential above the threshold potential the two H-atom removal could take place via concerted pathways. These steps represent rapid pre-equilibria before the rate determining step, which corresponds to the OO bond formation. The key chemical step occurs via nucleophilic attack of an external water molecule to intermediate S2. We assume that this step governs the kinetics of the reaction. Comparison of the calculated energetics and electronic structures of intermediate species in the PCo4 and VCo4 catalyzed water oxidation cycle shows that coupling of d orbitals of V and Co atoms in VCo4 increases the oxidation potential of the Co-center. The orbital coupling is also responsible for the higher catalytic activity of VCo4 because it increases the electrophilicity of CoIII moiety in the key S2 species.

Research group: Química Quàntica

Thematic Areas: Química Química Chemistry

licence for use: https://creativecommons.org/licenses/by/3.0/es/

ISSN: 0021-9517

Author identifier: 0000-0003-0322-6796; ; ; ; 0000-0002-3945-6721; 0000-0002-4533-0623

Record's date: 2018-03-05

Last page: 63

Journal volume: 350

Papper version: info:eu-repo/semantics/publishedVersion

Link to the original source: https://www.sciencedirect.com/science/article/pii/S0021951717301021?via%3Dihub

Funding program: plan; Excelencia; CTQ2014-52774-P altres; Grupos Consolidados; 2014SGR199 altres; ICREA Academia

Article's DOI: 10.1016/j.jcat.2017.03.018

Entity: Universitat Rovira i Virgili

Journal publication year: 2017

First page: 56

Publication Type: Article Artículo Article