Reaction dynamics of metal/oxide catalysts: Methanol oxidation at vanadium oxide films on Rh(1 1 1) from UHV to 10−2 mbar

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Bernhard von Boehn
  • Christopher Penschke
  • Xiaoke Li
  • Joachim Paier
  • Joachim Sauer
  • Jon Olaf Krisponeit
  • Jan Ingo Flege
  • Jens Falta
  • Helder Marchetto
  • Torsten Franz
  • Gerhard Lilienkamp
  • Ronald Imbihl

Externe Organisationen

  • Humboldt-Universität zu Berlin (HU Berlin)
  • Universität Bremen
  • Brandenburgische Technische Universität Cottbus - Senftenberg (BTU)
  • Technische Universität Clausthal
  • ELMITEC Elektronenmikroskopie GmbH
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)255-264
Seitenumfang10
FachzeitschriftJournal of catalysis
Jahrgang385
Frühes Online-Datum5 Apr. 2020
PublikationsstatusVeröffentlicht - Mai 2020

Abstract

Recent advances in in situ microscopy allow to follow the reaction dynamics during a catalytic surface reaction from ultra-high vacuum to 0.1 mbar, thus bridging a large part of the pressure gap. Submonolayer vanadium oxide films on Rh(1 1 1) have been studied during catalytic methanol oxidation in situ with spatially resolving imaging techniques. At 10−6–10−4 mbar VOx condenses into macroscopic circular islands that exhibit a substructure, consisting of a reduced island core and an oxidized outer ring. This substructure arises due to an oxygen gradient inside the VOx islands, which results in different coexisting 2D-phases of VOx on Rh(1 1 1). This substructure is also responsible for a “breathing-like” oscillatory expansion and contraction that the islands undergo under stationary conditions. Using density functional theory, the 2D-phase diagram of VOx on Rh(1 1 1) has been computed. The oscillatory behavior can be understood as a periodic phase transition between two 2D phases of VOx. With a newly developed near ambient pressure – low-energy electron microscope, it was shown that VOx islands disintegrate at 10−2 mbar, resulting in turbulent dynamics.

ASJC Scopus Sachgebiete

Zitieren

Reaction dynamics of metal/oxide catalysts: Methanol oxidation at vanadium oxide films on Rh(1 1 1) from UHV to 10−2 mbar. / von Boehn, Bernhard; Penschke, Christopher; Li, Xiaoke et al.
in: Journal of catalysis, Jahrgang 385, 05.2020, S. 255-264.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

von Boehn, B, Penschke, C, Li, X, Paier, J, Sauer, J, Krisponeit, JO, Flege, JI, Falta, J, Marchetto, H, Franz, T, Lilienkamp, G & Imbihl, R 2020, 'Reaction dynamics of metal/oxide catalysts: Methanol oxidation at vanadium oxide films on Rh(1 1 1) from UHV to 10−2 mbar', Journal of catalysis, Jg. 385, S. 255-264. https://doi.org/10.1016/j.jcat.2020.03.016
von Boehn, B., Penschke, C., Li, X., Paier, J., Sauer, J., Krisponeit, J. O., Flege, J. I., Falta, J., Marchetto, H., Franz, T., Lilienkamp, G., & Imbihl, R. (2020). Reaction dynamics of metal/oxide catalysts: Methanol oxidation at vanadium oxide films on Rh(1 1 1) from UHV to 10−2 mbar. Journal of catalysis, 385, 255-264. https://doi.org/10.1016/j.jcat.2020.03.016
von Boehn B, Penschke C, Li X, Paier J, Sauer J, Krisponeit JO et al. Reaction dynamics of metal/oxide catalysts: Methanol oxidation at vanadium oxide films on Rh(1 1 1) from UHV to 10−2 mbar. Journal of catalysis. 2020 Mai;385:255-264. Epub 2020 Apr 5. doi: 10.1016/j.jcat.2020.03.016
von Boehn, Bernhard ; Penschke, Christopher ; Li, Xiaoke et al. / Reaction dynamics of metal/oxide catalysts : Methanol oxidation at vanadium oxide films on Rh(1 1 1) from UHV to 10−2 mbar. in: Journal of catalysis. 2020 ; Jahrgang 385. S. 255-264.
Download
@article{4f6f2730fd704a5393eb8561a44376d3,
title = "Reaction dynamics of metal/oxide catalysts: Methanol oxidation at vanadium oxide films on Rh(1 1 1) from UHV to 10−2 mbar",
abstract = "Recent advances in in situ microscopy allow to follow the reaction dynamics during a catalytic surface reaction from ultra-high vacuum to 0.1 mbar, thus bridging a large part of the pressure gap. Submonolayer vanadium oxide films on Rh(1 1 1) have been studied during catalytic methanol oxidation in situ with spatially resolving imaging techniques. At 10−6–10−4 mbar VOx condenses into macroscopic circular islands that exhibit a substructure, consisting of a reduced island core and an oxidized outer ring. This substructure arises due to an oxygen gradient inside the VOx islands, which results in different coexisting 2D-phases of VOx on Rh(1 1 1). This substructure is also responsible for a “breathing-like” oscillatory expansion and contraction that the islands undergo under stationary conditions. Using density functional theory, the 2D-phase diagram of VOx on Rh(1 1 1) has been computed. The oscillatory behavior can be understood as a periodic phase transition between two 2D phases of VOx. With a newly developed near ambient pressure – low-energy electron microscope, it was shown that VOx islands disintegrate at 10−2 mbar, resulting in turbulent dynamics.",
keywords = "Heterogeneous catalysis, Inverse catalyst, Methanol oxidation, Near ambient pressure low-energy electron microscope, Pressure gap, Restructuring, Vanadium oxide",
author = "{von Boehn}, Bernhard and Christopher Penschke and Xiaoke Li and Joachim Paier and Joachim Sauer and Krisponeit, {Jon Olaf} and Flege, {Jan Ingo} and Jens Falta and Helder Marchetto and Torsten Franz and Gerhard Lilienkamp and Ronald Imbihl",
note = "Funding Information: This work was supported by a computer grant from the North German Computing Alliance Berlin?Hannover (HLRN). B. v. B. would like to thank the Department of Inorganic Chemistry of the Fritz Haber Institute of the Max Planck Society for financial support.",
year = "2020",
month = may,
doi = "10.1016/j.jcat.2020.03.016",
language = "English",
volume = "385",
pages = "255--264",
journal = "Journal of catalysis",
issn = "0021-9517",
publisher = "Academic Press Inc.",

}

Download

TY - JOUR

T1 - Reaction dynamics of metal/oxide catalysts

T2 - Methanol oxidation at vanadium oxide films on Rh(1 1 1) from UHV to 10−2 mbar

AU - von Boehn, Bernhard

AU - Penschke, Christopher

AU - Li, Xiaoke

AU - Paier, Joachim

AU - Sauer, Joachim

AU - Krisponeit, Jon Olaf

AU - Flege, Jan Ingo

AU - Falta, Jens

AU - Marchetto, Helder

AU - Franz, Torsten

AU - Lilienkamp, Gerhard

AU - Imbihl, Ronald

N1 - Funding Information: This work was supported by a computer grant from the North German Computing Alliance Berlin?Hannover (HLRN). B. v. B. would like to thank the Department of Inorganic Chemistry of the Fritz Haber Institute of the Max Planck Society for financial support.

PY - 2020/5

Y1 - 2020/5

N2 - Recent advances in in situ microscopy allow to follow the reaction dynamics during a catalytic surface reaction from ultra-high vacuum to 0.1 mbar, thus bridging a large part of the pressure gap. Submonolayer vanadium oxide films on Rh(1 1 1) have been studied during catalytic methanol oxidation in situ with spatially resolving imaging techniques. At 10−6–10−4 mbar VOx condenses into macroscopic circular islands that exhibit a substructure, consisting of a reduced island core and an oxidized outer ring. This substructure arises due to an oxygen gradient inside the VOx islands, which results in different coexisting 2D-phases of VOx on Rh(1 1 1). This substructure is also responsible for a “breathing-like” oscillatory expansion and contraction that the islands undergo under stationary conditions. Using density functional theory, the 2D-phase diagram of VOx on Rh(1 1 1) has been computed. The oscillatory behavior can be understood as a periodic phase transition between two 2D phases of VOx. With a newly developed near ambient pressure – low-energy electron microscope, it was shown that VOx islands disintegrate at 10−2 mbar, resulting in turbulent dynamics.

AB - Recent advances in in situ microscopy allow to follow the reaction dynamics during a catalytic surface reaction from ultra-high vacuum to 0.1 mbar, thus bridging a large part of the pressure gap. Submonolayer vanadium oxide films on Rh(1 1 1) have been studied during catalytic methanol oxidation in situ with spatially resolving imaging techniques. At 10−6–10−4 mbar VOx condenses into macroscopic circular islands that exhibit a substructure, consisting of a reduced island core and an oxidized outer ring. This substructure arises due to an oxygen gradient inside the VOx islands, which results in different coexisting 2D-phases of VOx on Rh(1 1 1). This substructure is also responsible for a “breathing-like” oscillatory expansion and contraction that the islands undergo under stationary conditions. Using density functional theory, the 2D-phase diagram of VOx on Rh(1 1 1) has been computed. The oscillatory behavior can be understood as a periodic phase transition between two 2D phases of VOx. With a newly developed near ambient pressure – low-energy electron microscope, it was shown that VOx islands disintegrate at 10−2 mbar, resulting in turbulent dynamics.

KW - Heterogeneous catalysis

KW - Inverse catalyst

KW - Methanol oxidation

KW - Near ambient pressure low-energy electron microscope

KW - Pressure gap

KW - Restructuring

KW - Vanadium oxide

UR - http://www.scopus.com/inward/record.url?scp=85082707953&partnerID=8YFLogxK

U2 - 10.1016/j.jcat.2020.03.016

DO - 10.1016/j.jcat.2020.03.016

M3 - Article

AN - SCOPUS:85082707953

VL - 385

SP - 255

EP - 264

JO - Journal of catalysis

JF - Journal of catalysis

SN - 0021-9517

ER -