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SiO-Rh(111) Interface: Stability and Activation of Small Molecules
Lan Chen1, Changle Mu1, Wuyang Song1
1State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, Fujian, China.
This study explores the SiO2-Rh interface, crucial for CO hydrogenation. Results show SiO2 films grow on Rh(111), and small molecules activate at this interface, enhancing catalyst performance.
Area of Science:
- Materials Science
- Surface Science
- Catalysis
Background:
- Rhodium (Rh) supported on silicon dioxide (SiO2) catalysts are vital for CO hydrogenation.
- Promoters enhance Rh/SiO2 catalyst activity and selectivity for C2 oxygenates.
- The Rh-SiO2 interface's structural and electronic properties require deeper investigation.
Purpose of the Study:
- To investigate the growth and stability of ultrathin SiO2 films on Rh(111).
- To explore the adsorption behavior of O2 and CO at the SiO2-Rh interface.
- To understand the electronic changes at the interface upon gas adsorption.
Main Methods:
- Silicon evaporation onto Rh(111) followed by O2 annealing to form SiO2 films.
- Analysis of film growth mode (layer-plus-island).
- Examination of interface stability under O2 pressure and vacuum annealing.
- X-ray photoelectron spectroscopy (XPS) to study binding energy shifts of Si 2p and O 1s.
Main Results:
- SiO2 films grow on Rh(111) in a layer-plus-island mode.
- The SiO2-Rh interface is stable under elevated O2 pressure and vacuum annealing.
- Both O2 and CO adsorb at the SiO2-Rh interface at elevated pressures.
- Adsorption of oxygen at the interface causes shifts in Si 2p and O 1s binding energies.
Conclusions:
- Evidence for small molecule activation at the metal-oxide interface.
- Demonstration of a passivation effect of oxide-coated metal surfaces.
- Provides fundamental insights into metal-oxide interfaces for catalytic applications.
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