Indium oxide has received attention as an exciting candidate for catalyzing the CO hydrogenation to methanol due to its high selectivity (>80%). Compared to the extent of research on the activity of indium oxide-based powder catalysts, very little is known about the phenomena associated with the formation of surface alloys involving indium or the growth mechanism for indium oxide nanoparticles. In this report, scanning tunneling microscopy and X-ray photoelectron spectroscopy (XPS) were employed to elucidate the growth mode, structure, and chemical state of In/Au(111) alloys and InO/Au(111) inverse model catalysts. Our study reveals distinct morphological differences between In/Au(111) and InO/Au(111), and the InO structure also depends strongly on the preparation conditions. In/Au surface alloy systems with extremely low coverage (0.02 ML) form islands preferentially on the elbow sites of reconstructed Au(111) herringbone, regardless of hexagonally closed packed and face centered cubic stacking. At higher coverage (0.1 ML), the In islands expand over the herringbone in the ⟨110⟩ direction and create two dimensional domain structures over the entire surfaces. Moreover, this 2D domain structure is disturbed by temperature with high dispersion of indium atoms observed during the annealing process. Oxidation of the In/Au(111) surface alloys with O at 550 K produces InO/Au(111) systems which contain various sizes of InO aggregates (from 0.7 nm to 10 nm). On the other hand, InO/Au(111) surfaces prepared by vapor deposition of In at 550 K in an O background exhibit highly dispersed and uniformly small InO particles (∼1 nm). Both InO systems were confirmed to be partially oxidized by XPS.
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http://dx.doi.org/10.1063/1.5139237 | DOI Listing |
ACS Omega
April 2024
Department of Chemistry, National Central University Chungli County, Taoyuan 320317, Taiwan, Republic of China.
A nickel film electroplated onto a metal substrate can be used as a catalyst for water splitting and a magnetic material for spin valves. Although the nucleation and growth of Ni on Au(111) have already been examined with in situ scanning tunneling microscopy (STM), the current study provides new insights of the structure of the first layer of Ni on an ordered Au(111) electrode in 0.1 M KSO + 1 mM HSO + 10 mM NiSO (pH 3).
View Article and Find Full Text PDFJ Chem Phys
January 2024
State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
The 6D time-dependent wave packet calculations were performed to explore H2 dissociation on Ag, Au, and two AgAu alloy surfaces, using four newly fitted potential energy surfaces based on the neural network fitting to density functional theory energy points. The ligand effect resulting from the Ag-Au interaction causes a reduction in the barrier height for H2+Ag/Au(111) compared to H2+Ag(111). However, the scenario is reversed for H2+Au/Ag(111) and H2+Au(111).
View Article and Find Full Text PDFACS Catal
December 2023
Thomas Young Centre and Department of Chemical Engineering, University College London, Roberts Building, Torrington Place, London WC1E 7JE, U.K.
Molecules
December 2023
Dipartimento di Scienze Chimiche e Farmaceutiche, Università degli Studi di Trieste, Via L. Giorgieri 1, I-34127 Trieste, Italy.
The surprisingly high catalytic activity of gold has been known to the heterogeneous catalysis community since the mid-1980s. Significant efforts have been directed towards improving the reactivity of these surfaces towards important industrial reactions. One such strategy is the introduction of small amounts of other metals to create Au-based surface alloys.
View Article and Find Full Text PDFJ Phys Chem Lett
November 2023
State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Understanding polar molecule dynamics on bimetallic surfaces, especially electropositivity and electronegativity, remains a challenge. Here, we report the reactivity of HCl on a strained Ag monolayer on Au(111) using six-dimensional quantum dynamics with a new machine-learning-based potential energy surface. Surprisingly, HCl reactivity is significantly suppressed by the Ag-Au interaction despite a lower HCl+Ag/Au(111) barrier than pure Ag(111).
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