Catalytic activity of Pt38 in the oxygen reduction reaction from first-principles simulations. Issue 18 (30th June 2016)

• Record Type: Journal Article
• Authors: Sementa, Luca; Andreussi, Oliviero; Goddard III, William A.; Fortunelli, Alessandro
• Is Part Of: Catalysis science & technology. Volume 6:Issue 18(2016)
• Page Start: 6901
• Page End: 6909
• Publication Date: 2016-06-30
• Subjects: Catalysis -- Periodicals; 541.395
• DOI: 10.1039/c6cy00750c
• Languages: English
• ISSNs: 2044-4753

Abstract

Abstract : Mechanism of OHads /Pt38 diffusion via transient hydronium species in first-principles molecular dynamics simulations. Abstract : The activity of truncated octahedral Pt38 clusters as a catalyst in the oxygen reduction reaction (ORR) is investigated via first-principles simulations. Three catalytic steps: O2 dissociation (O2ads → 2Oads ), O hydration (Oads + H2 Oads → 2OHads ), and H2 O formation (OHads + Hads → H2 Oads ) are considered, in which all reactant species are co-adsorbed on the Pt38 cluster according to a Langmuir–Hinshelwood mechanism. The minimum structures and saddle points for these different steps are then calculated at the density-functional theory (DFT) level using a gradient-corrected exchange–correlation (xc-)functional and taking into account the effect of the solvent via a self-consistent continuum solvation model. Moreover, first-principles molecular dynamics (AIMD) simulations in which the H2 O solvent is explicitly described are performed to explore dynamic phenomena such as fast hydrogen transfer via meta-stable hydronium-type configurations and their possible role in ORR reaction paths. By comparing the present findings with previous results on the Pt(111) surface, it is shown that in such a nanometer-size cluster the rate-determining-step (rds) corresponds to H2 O formation, at variance with the extended surface in which O hydration was rate-determining, and that the overall reaction barrier is actually increased with respect to the extended system. This is in agreement with and rationalizes experimental results showing a decrease of ORR catalytic activity in the nanometer-size cluster range.