Segregation dynamics of a Pd-Ag surface during CO oxidation investigated by NAP-XPS
(2022) In Catalysis Today 384-386. p.265-273- Abstract
The dynamic changes in composition in the near-surface region of a Pd75%Ag25%(100) single crystal were monitored using near-ambient pressure x-ray photoelectron spectroscopy (NAP-XPS) during CO oxidation under oxygen rich conditions at a total pressure of 1.1 mbar. Six CO oxidation temperature cycles were investigated at different heating rates and maximum temperatures of 450 °C or 600 °C. It was found that the history of the bimetallic sample plays an important role, as the CO2 formation profile varies depending on initial conditions, and previous heating rates and maximum temperatures. In terms of CO coverage effects, normal, reversed and no hysteresis behaviour were all observed. In agreement with... (More)
The dynamic changes in composition in the near-surface region of a Pd75%Ag25%(100) single crystal were monitored using near-ambient pressure x-ray photoelectron spectroscopy (NAP-XPS) during CO oxidation under oxygen rich conditions at a total pressure of 1.1 mbar. Six CO oxidation temperature cycles were investigated at different heating rates and maximum temperatures of 450 °C or 600 °C. It was found that the history of the bimetallic sample plays an important role, as the CO2 formation profile varies depending on initial conditions, and previous heating rates and maximum temperatures. In terms of CO coverage effects, normal, reversed and no hysteresis behaviour were all observed. In agreement with previous modelling predictions, the NAP-XPS data confirm a dynamic segregation behaviour upon heating/cooling where the amount of Pd in the surface region decreases with increasing temperature. Nevertheless, the Pd 3d5/2 core level relative area assessment is not fully capable of capturing all the surface dynamics inferred from the temperature dependent CO2 formation profiles, due to the probing depth. While residing at ambient temperature in the reaction mixture, however, there is a build-up of adsorbed CO at the surface showing that CO induces segregation of Pd to the topmost surface layer under these conditions. In total, this suggests that the segregation is kinetically relatively facile during temperature cycling, and that adsorbate coverage is the main controlling factor for the surface termination.
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- author
- Strømsheim, Marie D. ; Svenum, Ingeborg Helene ; Mahmoodinia, Mehdi ; Boix, Virgínia LU ; Knudsen, Jan LU and Venvik, Hilde J.
- organization
- publishing date
- 2022
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Bimetallic catalysis, Carbon monoxide oxidation, Palladium, Segregation, Silver, Single crystal surface
- in
- Catalysis Today
- volume
- 384-386
- pages
- 265 - 273
- publisher
- Elsevier
- external identifiers
-
- scopus:85102300997
- ISSN
- 0920-5861
- DOI
- 10.1016/j.cattod.2021.02.007
- language
- English
- LU publication?
- yes
- id
- dd1b5ab4-887f-49b6-8538-84e944d5c2c9
- date added to LUP
- 2021-03-29 08:35:19
- date last changed
- 2023-11-08 12:47:27
@article{dd1b5ab4-887f-49b6-8538-84e944d5c2c9,
abstract = {{<p>The dynamic changes in composition in the near-surface region of a Pd<sub>75%</sub>Ag<sub>25%</sub>(100) single crystal were monitored using near-ambient pressure x-ray photoelectron spectroscopy (NAP-XPS) during CO oxidation under oxygen rich conditions at a total pressure of 1.1 mbar. Six CO oxidation temperature cycles were investigated at different heating rates and maximum temperatures of 450 °C or 600 °C. It was found that the history of the bimetallic sample plays an important role, as the CO<sub>2</sub> formation profile varies depending on initial conditions, and previous heating rates and maximum temperatures. In terms of CO coverage effects, normal, reversed and no hysteresis behaviour were all observed. In agreement with previous modelling predictions, the NAP-XPS data confirm a dynamic segregation behaviour upon heating/cooling where the amount of Pd in the surface region decreases with increasing temperature. Nevertheless, the Pd 3d<sub>5/2</sub> core level relative area assessment is not fully capable of capturing all the surface dynamics inferred from the temperature dependent CO<sub>2</sub> formation profiles, due to the probing depth. While residing at ambient temperature in the reaction mixture, however, there is a build-up of adsorbed CO at the surface showing that CO induces segregation of Pd to the topmost surface layer under these conditions. In total, this suggests that the segregation is kinetically relatively facile during temperature cycling, and that adsorbate coverage is the main controlling factor for the surface termination.</p>}},
author = {{Strømsheim, Marie D. and Svenum, Ingeborg Helene and Mahmoodinia, Mehdi and Boix, Virgínia and Knudsen, Jan and Venvik, Hilde J.}},
issn = {{0920-5861}},
keywords = {{Bimetallic catalysis; Carbon monoxide oxidation; Palladium; Segregation; Silver; Single crystal surface}},
language = {{eng}},
pages = {{265--273}},
publisher = {{Elsevier}},
series = {{Catalysis Today}},
title = {{Segregation dynamics of a Pd-Ag surface during CO oxidation investigated by NAP-XPS}},
url = {{http://dx.doi.org/10.1016/j.cattod.2021.02.007}},
doi = {{10.1016/j.cattod.2021.02.007}},
volume = {{384-386}},
year = {{2022}},
}