Andrea Resta - Academia.edu (original) (raw)
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Papers by Andrea Resta
Journal of Physical Chemistry C, Sep 16, 2020
The reaction of ammonia oxidation over PtRh binary alloy has been studied with a surface science ... more The reaction of ammonia oxidation over PtRh binary alloy has been studied with a surface science approach by operando techniques such as Near Ambient Pressure X-Ray Photoemission Spectroscopy (NAP-...
ACS Applied Materials & Interfaces, Jul 28, 2020
The Journal of Physical Chemistry C, 2021
ACS Applied Materials & Interfaces, 2020
The Journal of Physical Chemistry C, 2020
ACS Applied Nano Materials, 2019
The Journal of Physical Chemistry C, 2007
Using a variety of dedicated surface sensitive techniques, we studied the interaction of hydrogen... more Using a variety of dedicated surface sensitive techniques, we studied the interaction of hydrogen with bare and adsorbate modified RuO2 (110) surfaces on the atomic scale. Hydrogen interacts strongly with the undercoordinated O atoms, thereby forming hydroxyl ...
The Journal of Physical Chemistry C, 2009
ABSTRACT The adsorption of CO on nanosized gold particles deposited on a cerium oxide substrate i... more ABSTRACT The adsorption of CO on nanosized gold particles deposited on a cerium oxide substrate is strongly influenced by the roughness and concentration of oxygen vacancies of the CeOx substrate surface. Literature showed that Au nucleates at step edges on oxidized samples. For oxidized samples we found that the Au dispersion is dependent on the surface roughness. A rough CeO2 surface has a higher step density, which results in a Au higher particle density with a smaller average diameter. Other studies showed that Au nucleates on oxygen vacancies on reduced CeOx substrates. We found that small Au particles adsorbed on oxygen vacancies exhibit a significantly higher Au 4f binding energy than Au particles on oxidized CeO2. Relatively less CO adsorbs on small Au particles on a reduced substrate, with a significantly lower adsorption energy than on Au on an oxidized substrate. For larger particles the influence of oxygen vacancies in the substrate is negligible.
The Journal of Physical Chemistry C, 2007
Soft X-ray photoelectron spectroscopy (SXPS) and X-ray absorption near-edge structure (XANES) hav... more Soft X-ray photoelectron spectroscopy (SXPS) and X-ray absorption near-edge structure (XANES) have been combined with low-energy electron diffraction (LEED) to examine the growth of titanium dioxide thin films on Ni (110). Depending on the initial titanium ...
The Journal of Physical Chemistry C, 2010
ABSTRACT Using a combination of surface X-ray diffraction and mass spectrometry at realistic pres... more ABSTRACT Using a combination of surface X-ray diffraction and mass spectrometry at realistic pressures, the CO oxidation reactivity of a Rh(111) model catalyst has been studied in conjunction with the surface structure. The measurements show that a specific thin surface oxide is always present in the high activity regime of Rh-based CO oxidation.
The Journal of Physical Chemistry C, 2008
The Journal of Physical Chemistry B, 2006
The Journal of Physical Chemistry B, 2006
Journal of Physical Chemistry C, Sep 16, 2020
The reaction of ammonia oxidation over PtRh binary alloy has been studied with a surface science ... more The reaction of ammonia oxidation over PtRh binary alloy has been studied with a surface science approach by operando techniques such as Near Ambient Pressure X-Ray Photoemission Spectroscopy (NAP-...
ACS Applied Materials & Interfaces, Jul 28, 2020
The Journal of Physical Chemistry C, 2021
ACS Applied Materials & Interfaces, 2020
The Journal of Physical Chemistry C, 2020
ACS Applied Nano Materials, 2019
The Journal of Physical Chemistry C, 2007
Using a variety of dedicated surface sensitive techniques, we studied the interaction of hydrogen... more Using a variety of dedicated surface sensitive techniques, we studied the interaction of hydrogen with bare and adsorbate modified RuO2 (110) surfaces on the atomic scale. Hydrogen interacts strongly with the undercoordinated O atoms, thereby forming hydroxyl ...
The Journal of Physical Chemistry C, 2009
ABSTRACT The adsorption of CO on nanosized gold particles deposited on a cerium oxide substrate i... more ABSTRACT The adsorption of CO on nanosized gold particles deposited on a cerium oxide substrate is strongly influenced by the roughness and concentration of oxygen vacancies of the CeOx substrate surface. Literature showed that Au nucleates at step edges on oxidized samples. For oxidized samples we found that the Au dispersion is dependent on the surface roughness. A rough CeO2 surface has a higher step density, which results in a Au higher particle density with a smaller average diameter. Other studies showed that Au nucleates on oxygen vacancies on reduced CeOx substrates. We found that small Au particles adsorbed on oxygen vacancies exhibit a significantly higher Au 4f binding energy than Au particles on oxidized CeO2. Relatively less CO adsorbs on small Au particles on a reduced substrate, with a significantly lower adsorption energy than on Au on an oxidized substrate. For larger particles the influence of oxygen vacancies in the substrate is negligible.
The Journal of Physical Chemistry C, 2007
Soft X-ray photoelectron spectroscopy (SXPS) and X-ray absorption near-edge structure (XANES) hav... more Soft X-ray photoelectron spectroscopy (SXPS) and X-ray absorption near-edge structure (XANES) have been combined with low-energy electron diffraction (LEED) to examine the growth of titanium dioxide thin films on Ni (110). Depending on the initial titanium ...
The Journal of Physical Chemistry C, 2010
ABSTRACT Using a combination of surface X-ray diffraction and mass spectrometry at realistic pres... more ABSTRACT Using a combination of surface X-ray diffraction and mass spectrometry at realistic pressures, the CO oxidation reactivity of a Rh(111) model catalyst has been studied in conjunction with the surface structure. The measurements show that a specific thin surface oxide is always present in the high activity regime of Rh-based CO oxidation.
The Journal of Physical Chemistry C, 2008
The Journal of Physical Chemistry B, 2006
The Journal of Physical Chemistry B, 2006