Dynamics of subsurface oxygen formation in catalytic water formation on a Rh(1 1 1) surface: Experiment and simulation

Research output: Contribution to journalConference articleResearchpeer review

Authors

  • M. I. Monine
  • A. Schaak
  • B. Y. Rubinstein
  • R. Imbihl
  • L. M. Pismen

External Research Organisations

  • Technion-Israel Institute of Technology
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Details

Original languageEnglish
Pages (from-to)321-330
Number of pages10
JournalCatalysis today
Volume70
Issue number4
Publication statusPublished - 1 Nov 2001
EventSpatiotemporal Catalytic Patterns (SHEINTUCH S.I.) - Haifa, Israel
Duration: 15 Oct 200015 Oct 2000

Abstract

The catalytic O2+H2 reaction on Rh(1 1 1) has been investigated in the 10-6-10-5mbar range using photoelectron emission microscopy as spatially resolving method. While the reaction without pretreatment of the sample displays simple bistable behavior, we find that after extended pre-oxidation of the sample (pO(2) = 2 × 10-4mbar,T = 770 K, tOX > 24 h), low work function (LWF) areas develop dynamically in the collision of reaction fronts. The LWF areas have been assigned to subsurface oxygen. We present a simple three-variable model which reproduces the formation of LWF areas in the collision of reaction fronts.

Keywords

    Low work function, Photoelectron emission microscopy, Subsurface oxygen formation

ASJC Scopus subject areas

Cite this

Dynamics of subsurface oxygen formation in catalytic water formation on a Rh(1 1 1) surface: Experiment and simulation. / Monine, M. I.; Schaak, A.; Rubinstein, B. Y. et al.
In: Catalysis today, Vol. 70, No. 4, 01.11.2001, p. 321-330.

Research output: Contribution to journalConference articleResearchpeer review

Monine MI, Schaak A, Rubinstein BY, Imbihl R, Pismen LM. Dynamics of subsurface oxygen formation in catalytic water formation on a Rh(1 1 1) surface: Experiment and simulation. Catalysis today. 2001 Nov 1;70(4):321-330. doi: 10.1016/S0920-5861(01)00340-6
Monine, M. I. ; Schaak, A. ; Rubinstein, B. Y. et al. / Dynamics of subsurface oxygen formation in catalytic water formation on a Rh(1 1 1) surface : Experiment and simulation. In: Catalysis today. 2001 ; Vol. 70, No. 4. pp. 321-330.
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abstract = "The catalytic O2+H2 reaction on Rh(1 1 1) has been investigated in the 10-6-10-5mbar range using photoelectron emission microscopy as spatially resolving method. While the reaction without pretreatment of the sample displays simple bistable behavior, we find that after extended pre-oxidation of the sample (pO(2) = 2 × 10-4mbar,T = 770 K, tOX > 24 h), low work function (LWF) areas develop dynamically in the collision of reaction fronts. The LWF areas have been assigned to subsurface oxygen. We present a simple three-variable model which reproduces the formation of LWF areas in the collision of reaction fronts.",
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note = "Funding Information: This work has been supported by the German–Israeli Science Foundation. M.M and L.P. acknowledge the support by the Minerva Center for Nonlinear Physics of Complex Systems.; Spatiotemporal Catalytic Patterns (SHEINTUCH S.I.) ; Conference date: 15-10-2000 Through 15-10-2000",
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T1 - Dynamics of subsurface oxygen formation in catalytic water formation on a Rh(1 1 1) surface

T2 - Spatiotemporal Catalytic Patterns (SHEINTUCH S.I.)

AU - Monine, M. I.

AU - Schaak, A.

AU - Rubinstein, B. Y.

AU - Imbihl, R.

AU - Pismen, L. M.

N1 - Funding Information: This work has been supported by the German–Israeli Science Foundation. M.M and L.P. acknowledge the support by the Minerva Center for Nonlinear Physics of Complex Systems.

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Y1 - 2001/11/1

N2 - The catalytic O2+H2 reaction on Rh(1 1 1) has been investigated in the 10-6-10-5mbar range using photoelectron emission microscopy as spatially resolving method. While the reaction without pretreatment of the sample displays simple bistable behavior, we find that after extended pre-oxidation of the sample (pO(2) = 2 × 10-4mbar,T = 770 K, tOX > 24 h), low work function (LWF) areas develop dynamically in the collision of reaction fronts. The LWF areas have been assigned to subsurface oxygen. We present a simple three-variable model which reproduces the formation of LWF areas in the collision of reaction fronts.

AB - The catalytic O2+H2 reaction on Rh(1 1 1) has been investigated in the 10-6-10-5mbar range using photoelectron emission microscopy as spatially resolving method. While the reaction without pretreatment of the sample displays simple bistable behavior, we find that after extended pre-oxidation of the sample (pO(2) = 2 × 10-4mbar,T = 770 K, tOX > 24 h), low work function (LWF) areas develop dynamically in the collision of reaction fronts. The LWF areas have been assigned to subsurface oxygen. We present a simple three-variable model which reproduces the formation of LWF areas in the collision of reaction fronts.

KW - Low work function

KW - Photoelectron emission microscopy

KW - Subsurface oxygen formation

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