Nucleation of chemical waves at structural defects: A mirror electron microscopy study of catalytic CO oxidation on Pt(110)

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • K. C. Rose
  • R. Imbihl
  • B. Rausenberger
  • C. S. Rastomjee
  • W. Engel
  • A. M. Bradshaw

Externe Organisationen

  • Fritz-Haber-Institut der Max-Planck-Gesellschaft
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)258-262
Seitenumfang5
FachzeitschriftSurface science
Jahrgang352-354
PublikationsstatusVeröffentlicht - 15 Mai 1996

Abstract

The formation of reaction fronts during the catalytic oxidation of CO on Pt(110) has been investigated with mirror electron microscopy (MEM). The reaction was studied in the 10-5 mbar range at T ≈ 430-450 K under conditions where spatio-temporal pattern formation occurs. Nucleation of reaction fronts was always found to take place at surface defects. While the CO front nucleates as a circular spot, the oxygen front first spreads out very rapidly along the [110] direction. Often, the reaction fronts fail to propagate away entirely from the defects, and instead a kind of breathing mode is observed. Rotating spiral waves can be identified, the cores of which are not attached to structural defects, but meander freely.

ASJC Scopus Sachgebiete

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Nucleation of chemical waves at structural defects: A mirror electron microscopy study of catalytic CO oxidation on Pt(110). / Rose, K. C.; Imbihl, R.; Rausenberger, B. et al.
in: Surface science, Jahrgang 352-354, 15.05.1996, S. 258-262.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Rose KC, Imbihl R, Rausenberger B, Rastomjee CS, Engel W, Bradshaw AM. Nucleation of chemical waves at structural defects: A mirror electron microscopy study of catalytic CO oxidation on Pt(110). Surface science. 1996 Mai 15;352-354:258-262. doi: 10.1016/0039-6028(95)01143-9
Rose, K. C. ; Imbihl, R. ; Rausenberger, B. et al. / Nucleation of chemical waves at structural defects : A mirror electron microscopy study of catalytic CO oxidation on Pt(110). in: Surface science. 1996 ; Jahrgang 352-354. S. 258-262.
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abstract = "The formation of reaction fronts during the catalytic oxidation of CO on Pt(110) has been investigated with mirror electron microscopy (MEM). The reaction was studied in the 10-5 mbar range at T ≈ 430-450 K under conditions where spatio-temporal pattern formation occurs. Nucleation of reaction fronts was always found to take place at surface defects. While the CO front nucleates as a circular spot, the oxygen front first spreads out very rapidly along the [110] direction. Often, the reaction fronts fail to propagate away entirely from the defects, and instead a kind of breathing mode is observed. Rotating spiral waves can be identified, the cores of which are not attached to structural defects, but meander freely.",
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T1 - Nucleation of chemical waves at structural defects

T2 - A mirror electron microscopy study of catalytic CO oxidation on Pt(110)

AU - Rose, K. C.

AU - Imbihl, R.

AU - Rausenberger, B.

AU - Rastomjee, C. S.

AU - Engel, W.

AU - Bradshaw, A. M.

N1 - Funding Information: This work has been supportedin part by the Fonds der ChemischenIn dustriea s well as by the DeutscheF orschungsgemeinschtahfrto ught he Son-derforschungsbere2ic9h0 .

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AB - The formation of reaction fronts during the catalytic oxidation of CO on Pt(110) has been investigated with mirror electron microscopy (MEM). The reaction was studied in the 10-5 mbar range at T ≈ 430-450 K under conditions where spatio-temporal pattern formation occurs. Nucleation of reaction fronts was always found to take place at surface defects. While the CO front nucleates as a circular spot, the oxygen front first spreads out very rapidly along the [110] direction. Often, the reaction fronts fail to propagate away entirely from the defects, and instead a kind of breathing mode is observed. Rotating spiral waves can be identified, the cores of which are not attached to structural defects, but meander freely.

KW - Carbon monoxide

KW - Catalysis

KW - Low index single crystal surfaces

KW - Low-energy electron microscopy (LEEM)

KW - Models of non-linear phenomena

KW - Oxygen

KW - Platinum

KW - Surface chemical reaction

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JO - Surface science

JF - Surface science

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