Reactivity and Stability of Ultrathin VOx Films on Pt(111) in Catalytic Methanol Oxidation

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Bernhard von Boehn
  • Lena Scholtz
  • Ronald Imbihl
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Details

OriginalspracheEnglisch
Seiten (von - bis)1545-1556
Seitenumfang12
FachzeitschriftTopics in catalysis
Jahrgang63
Ausgabenummer15-18
Frühes Online-Datum31 Juli 2020
PublikationsstatusVeröffentlicht - Nov. 2020

Abstract

The growth of ultrathin layers of VOx (< 12 monolayers) on Pt(111) and the activity of these layers in catalytic methanol oxidation at 10−4 mbar have been studied with low-energy electron diffraction, Auger electron spectroscopy, rate measurements, and with photoemission electron microscopy. Reactive deposition of V in O2 at 670 K obeys a Stranski–Krastanov growth mode with a (√3 × √3)R30° structure representing the limiting case for epitaxial growth of 3D-VOx. The activity of VOx/Pt(111) in catalytic methanol oxidation is very low and no redistribution dynamics is observed lifting the initial spatial homogeneity of the VOx layer. Under reaction conditions, part of the surface vanadium diffuses into the Pt subsurface region. Exposure to O2 causes part of the V to diffuse back to the surface, but only up to one monolayer of VOx can be stabilized in this way at 10−4 mbar.

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Reactivity and Stability of Ultrathin VOx Films on Pt(111) in Catalytic Methanol Oxidation. / von Boehn, Bernhard; Scholtz, Lena; Imbihl, Ronald.
in: Topics in catalysis, Jahrgang 63, Nr. 15-18, 11.2020, S. 1545-1556.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

von Boehn B, Scholtz L, Imbihl R. Reactivity and Stability of Ultrathin VOx Films on Pt(111) in Catalytic Methanol Oxidation. Topics in catalysis. 2020 Nov;63(15-18):1545-1556. Epub 2020 Jul 31. doi: 10.1007/s11244-020-01321-z, 10.1007/s11244-020-01373-1
von Boehn, Bernhard ; Scholtz, Lena ; Imbihl, Ronald. / Reactivity and Stability of Ultrathin VOx Films on Pt(111) in Catalytic Methanol Oxidation. in: Topics in catalysis. 2020 ; Jahrgang 63, Nr. 15-18. S. 1545-1556.
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abstract = "The growth of ultrathin layers of VOx (< 12 monolayers) on Pt(111) and the activity of these layers in catalytic methanol oxidation at 10−4 mbar have been studied with low-energy electron diffraction, Auger electron spectroscopy, rate measurements, and with photoemission electron microscopy. Reactive deposition of V in O2 at 670 K obeys a Stranski–Krastanov growth mode with a (√3 × √3)R30° structure representing the limiting case for epitaxial growth of 3D-VOx. The activity of VOx/Pt(111) in catalytic methanol oxidation is very low and no redistribution dynamics is observed lifting the initial spatial homogeneity of the VOx layer. Under reaction conditions, part of the surface vanadium diffuses into the Pt subsurface region. Exposure to O2 causes part of the V to diffuse back to the surface, but only up to one monolayer of VOx can be stabilized in this way at 10−4 mbar.",
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author = "{von Boehn}, Bernhard and Lena Scholtz and Ronald Imbihl",
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T1 - Reactivity and Stability of Ultrathin VOx Films on Pt(111) in Catalytic Methanol Oxidation

AU - von Boehn, Bernhard

AU - Scholtz, Lena

AU - Imbihl, Ronald

N1 - Funding Information: Open Access funding provided by Projekt DEAL. Bernhard von Boehn would like to thank the Department of Inorganic Chemistry of the Fritz Haber Institute of the Max Planck Society for financial support.

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N2 - The growth of ultrathin layers of VOx (< 12 monolayers) on Pt(111) and the activity of these layers in catalytic methanol oxidation at 10−4 mbar have been studied with low-energy electron diffraction, Auger electron spectroscopy, rate measurements, and with photoemission electron microscopy. Reactive deposition of V in O2 at 670 K obeys a Stranski–Krastanov growth mode with a (√3 × √3)R30° structure representing the limiting case for epitaxial growth of 3D-VOx. The activity of VOx/Pt(111) in catalytic methanol oxidation is very low and no redistribution dynamics is observed lifting the initial spatial homogeneity of the VOx layer. Under reaction conditions, part of the surface vanadium diffuses into the Pt subsurface region. Exposure to O2 causes part of the V to diffuse back to the surface, but only up to one monolayer of VOx can be stabilized in this way at 10−4 mbar.

AB - The growth of ultrathin layers of VOx (< 12 monolayers) on Pt(111) and the activity of these layers in catalytic methanol oxidation at 10−4 mbar have been studied with low-energy electron diffraction, Auger electron spectroscopy, rate measurements, and with photoemission electron microscopy. Reactive deposition of V in O2 at 670 K obeys a Stranski–Krastanov growth mode with a (√3 × √3)R30° structure representing the limiting case for epitaxial growth of 3D-VOx. The activity of VOx/Pt(111) in catalytic methanol oxidation is very low and no redistribution dynamics is observed lifting the initial spatial homogeneity of the VOx layer. Under reaction conditions, part of the surface vanadium diffuses into the Pt subsurface region. Exposure to O2 causes part of the V to diffuse back to the surface, but only up to one monolayer of VOx can be stabilized in this way at 10−4 mbar.

KW - Methanol oxidation

KW - Pt(111)

KW - Stranski–Krastanow growth

KW - Supported catalyst

KW - vanadium oxide catalysts

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