Adsorption state of NO on Ir(111) surfaces under excess O2 coexisting condition
•The adsorption state of NO under O2 coexisting conditions on Ir(111) single-crystal surfaces was studied by NAP-XPS.•At room temperature, O2 causes a partial replacement of NO at hollow sites with atomic oxygen.•At elevated temperatures (200–250 °C), the adsorption of NO is significantly suppressed...
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Veröffentlicht in: | Surface science 2019-07, Vol.685, p.1-6 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | •The adsorption state of NO under O2 coexisting conditions on Ir(111) single-crystal surfaces was studied by NAP-XPS.•At room temperature, O2 causes a partial replacement of NO at hollow sites with atomic oxygen.•At elevated temperatures (200–250 °C), the adsorption of NO is significantly suppressed by high-density chemisorbed atomic oxygen.
Iridium (Ir) exhibits a good efficiency for reduction of NO under excess O2 coexisting conditions at temperatures higher than 250 °C. On the other hand, the advantage is lost at lower temperatures below 250 °C under O2 existence, compared to any other platinum group metals. In this study, adsorption behavior of NO on Ir(111) single-crystal surfaces under excess O2 coexisting conditions at the temperatures from room temperature to 250 °C has been studied by in-situ X-ray Photoelectron Spectroscopy (XPS). It is revealed that the coexisting O2 induces formation of a high-density chemisorbed atomic oxygen (O) phase and the atomic O phase suppresses adsorption of NO at on-top sites significantly, which suggests that the suppression of NO adsorption causes a decrease in the ability of NO reduction at the lower temperatures.
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ISSN: | 0039-6028 1879-2758 |
DOI: | 10.1016/j.susc.2019.01.015 |