Structural analyses of the c(2 × 4)-N + 2O and the (2 × 1)-N phases on Rh(110) by low-energy electron diffraction

Research output: Contribution to journalArticleResearchpeer review

Authors

  • M. Gierer
  • F. Mertens
  • H. Over
  • G. Ertl
  • R. Imbihl

External Research Organisations

  • Fritz Haber Institute of the Max Planck Society (FHI)
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Details

Original languageEnglish
Pages (from-to)L903-L908
JournalSurface science
Volume339
Issue number3
Publication statusPublished - 1 Oct 1995

Abstract

The LEED analysis of the Rh(110)-(2 × 1)-N phase supports convincingly the RhN-added-row model revealing a RhN bond length of 1.91 ± 0.04 A ̊. The atomic geometry of c(2 × 4)-N + 2O on Rh(110) reflects the structural elements found in the pure N and O phases: The type of the Rh(110) surface reconstruction is induced by the oxygen adsorption, and a missing-row reconstruction analogous to the Rh(110)-(2 × 2)p2mg-2O surface is observed. Oxygen occupies the threefold-coordinated fcc site along the densily-packed rows. Nitrogen, however, causes the O network of the Rh(110)-(2 × 2)p2mg-2O to rearrange in order to provide N-adsorption sites which are maximal apart from the surrounding O atoms and, in addition, retains the local chemisorption geometry as compared with the pure (2 × 1)-N phase. Both requirements are met by shifting every second O-zigzag chain along the [11̄0] direction by a substrate lattice vector and by adsorbing N in the long-bridge site at the bottom of the (1 × 2) troughs.

Keywords

    (LEED), Low-energy electron diffraction, Nitrogen, Oxygen, Rh(110)

ASJC Scopus subject areas

Cite this

Structural analyses of the c(2 × 4)-N + 2O and the (2 × 1)-N phases on Rh(110) by low-energy electron diffraction. / Gierer, M.; Mertens, F.; Over, H. et al.
In: Surface science, Vol. 339, No. 3, 01.10.1995, p. L903-L908.

Research output: Contribution to journalArticleResearchpeer review

Gierer M, Mertens F, Over H, Ertl G, Imbihl R. Structural analyses of the c(2 × 4)-N + 2O and the (2 × 1)-N phases on Rh(110) by low-energy electron diffraction. Surface science. 1995 Oct 1;339(3):L903-L908. doi: 10.1016/0039-6028(95)80055-7
Gierer, M. ; Mertens, F. ; Over, H. et al. / Structural analyses of the c(2 × 4)-N + 2O and the (2 × 1)-N phases on Rh(110) by low-energy electron diffraction. In: Surface science. 1995 ; Vol. 339, No. 3. pp. L903-L908.
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abstract = "The LEED analysis of the Rh(110)-(2 × 1)-N phase supports convincingly the RhN-added-row model revealing a RhN bond length of 1.91 ± 0.04 A ̊. The atomic geometry of c(2 × 4)-N + 2O on Rh(110) reflects the structural elements found in the pure N and O phases: The type of the Rh(110) surface reconstruction is induced by the oxygen adsorption, and a missing-row reconstruction analogous to the Rh(110)-(2 × 2)p2mg-2O surface is observed. Oxygen occupies the threefold-coordinated fcc site along the densily-packed rows. Nitrogen, however, causes the O network of the Rh(110)-(2 × 2)p2mg-2O to rearrange in order to provide N-adsorption sites which are maximal apart from the surrounding O atoms and, in addition, retains the local chemisorption geometry as compared with the pure (2 × 1)-N phase. Both requirements are met by shifting every second O-zigzag chain along the [1{\=1}0] direction by a substrate lattice vector and by adsorbing N in the long-bridge site at the bottom of the (1 × 2) troughs.",
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AU - Mertens, F.

AU - Over, H.

AU - Ertl, G.

AU - Imbihl, R.

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AB - The LEED analysis of the Rh(110)-(2 × 1)-N phase supports convincingly the RhN-added-row model revealing a RhN bond length of 1.91 ± 0.04 A ̊. The atomic geometry of c(2 × 4)-N + 2O on Rh(110) reflects the structural elements found in the pure N and O phases: The type of the Rh(110) surface reconstruction is induced by the oxygen adsorption, and a missing-row reconstruction analogous to the Rh(110)-(2 × 2)p2mg-2O surface is observed. Oxygen occupies the threefold-coordinated fcc site along the densily-packed rows. Nitrogen, however, causes the O network of the Rh(110)-(2 × 2)p2mg-2O to rearrange in order to provide N-adsorption sites which are maximal apart from the surrounding O atoms and, in addition, retains the local chemisorption geometry as compared with the pure (2 × 1)-N phase. Both requirements are met by shifting every second O-zigzag chain along the [11̄0] direction by a substrate lattice vector and by adsorbing N in the long-bridge site at the bottom of the (1 × 2) troughs.

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