Adsorbate-induced structural evolution changes the mechanism of CO oxidation on a Rh/Fe3O4(001) model catalyst. Issue 10 (27th February 2020)

• Record Type: Journal Article
• Authors: Jakub, Zdenek; Hulva, Jan; Ryan, Paul T. P.; Duncan, David A.; Payne, David J.; Bliem, Roland; Ulreich, Manuel; Hofegger, Patrick; Kraushofer, Florian; Meier, Matthias; Schmid, Michael; Diebold, Ulrike; Parkinson, Gareth S.
• Is Part Of: Nanoscale. Volume 12:Issue 10(2020)
• Page Start: 5866
• Page End: 5875
• Publication Date: 2020-02-27
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/c9nr10087c
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : The Rh1 /Fe3 O4 (001) "single-atom" catalyst evolves differently upon exposure to O2 and CO, which results in distinct mechanisms of CO2 production. Abstract : The structure of a catalyst often changes in reactive environments, and following the structural evolution is crucial for the identification of the catalyst's active phase and reaction mechanism. Here we present an atomic-scale study of CO oxidation on a model Rh/Fe3 O4 (001) "single-atom" catalyst, which has a very different evolution depending on which of the two reactants, O2 or CO, is adsorbed first. Using temperature-programmed desorption (TPD) combined with scanning tunneling microscopy (STM) and X-ray photoelectron spectroscopy (XPS), we show that O2 destabilizes Rh atoms, leading to the formation of Rh x O y clusters; these catalyze CO oxidation via a Langmuir–Hinshelwood mechanism at temperatures as low as 200 K. If CO adsorbs first, the system is poisoned for direct interaction with O2, and CO oxidation is dominated by a Mars-van-Krevelen pathway at 480 K.