4.7 Article

Surface hydroxyl dependent adsorption of ruthenium on SiO2(001)-Understanding metal-support interaction

期刊

APPLIED SURFACE SCIENCE
卷 593, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.apsusc.2022.153396

关键词

Ruthenium; Silica; Surface hydroxyl; Metal-Support Interaction; DFT

资金

  1. Transformational Technologies for Clean Energy and Demonstration, Strategic Priority Research Program of the Chinese Academy of Sciences [XDA 21000000, XDA21020100]
  2. Synfuels China, Co. Ltd
  3. BMBF
  4. state of Mecklenburg-Vorpommern, Germany

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In this study, we computed the adsorption structures and energies of ruthenium on SiO2(001) surfaces and found that the adsorption of ruthenium atoms depends on the presence of surface hydroxyl groups. This finding is significant for understanding the structure, stability, and activity of silica supported ruthenium catalysts and catalysis.
To understand the metal-support interaction of oxide supported transition metal catalysts, we computed the adsorption structures and energies of ruthenium on the idealized SiO2(0 0 1) surfaces with full (OH, 100%), partial (OH, 50%) surface hydroxyl and without surface hydroxyl (OH, 0%) at different ruthenium loading. On the fully (up to 9Ru) and partially (up to 6Ru) hydroxylated surfaces, ruthenium adsorption prefers surface O-H oxidative addition and forms regularly distributed Ru(H)(2) species. After the reductive and re-combinative desorption of H-2, the adsorbed ruthenium atoms prefer structures with aggregated 2Ru dimeric units on the fully hydroxylated surface, while structures of remote and dispersed singly adsorbed Ru atoms on the partially hydroxylated surface. On the hydroxyl free surface (up to 6Ru), the adsorbed ruthenium atoms prefer threedimensional aggregated structures, which become more stable with the increase of ruthenium loading. This indicates the surface hydroxyl dependent ruthenium adsorption on SiO2 (001), and this finding is important for understanding the structure, stability and activity of silica supported ruthenium catalysts and catalysis.

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