Structure analysis of an oxidized nickel (110) surface using low energy ion scattering

L. K. Verheij; J. A. Van Den Berg; D. G. Armour

doi:10.1016/0039-6028(79)90145-6

Structure analysis of an oxidized nickel (110) surface using low energy ion scattering

L. K. Verheij, J. A. Van Den Berg, D. G. Armour

Research output: Contribution to journal › Article › peer-review

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Abstract

Low energy (6 keV) argon and neon ion scattering in the low angle mode (θ = 30°) has been used to investigate changes in the surface structure of a Ni(110) surface caused by the adsorption of oxygen at low exposures (10^-6 Torr s). The experimental energy spectra indicate that due to adsorption of oxygen, the interatomic distance in the 〈1̄10〉 direction increases while in the 〈001̄〉 direction this distance seems to decrease. This represents strong evidence that a reconstruction process is taking place during the early stages of oxidation of the Ni(110) face, in which the interatomic distances in the 〈1̄10〉 direction doubles. The oxygen atoms were found to lie in or close to the nickel 〈001̄〉 rows. These results are not in agreement with recently published dynamical LEED calculations.

Original language	English
Pages (from-to)	408-426
Number of pages	19
Journal	Surface Science
Volume	84
Issue number	2
DOIs	https://doi.org/10.1016/0039-6028(79)90145-6
Publication status	Published - 1 Jun 1979
Externally published	Yes

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title = "Structure analysis of an oxidized nickel (110) surface using low energy ion scattering",

abstract = "Low energy (6 keV) argon and neon ion scattering in the low angle mode (θ = 30°) has been used to investigate changes in the surface structure of a Ni(110) surface caused by the adsorption of oxygen at low exposures (10-6 Torr s). The experimental energy spectra indicate that due to adsorption of oxygen, the interatomic distance in the 〈{\=1}10〉 direction increases while in the 〈00{\=1}〉 direction this distance seems to decrease. This represents strong evidence that a reconstruction process is taking place during the early stages of oxidation of the Ni(110) face, in which the interatomic distances in the 〈{\=1}10〉 direction doubles. The oxygen atoms were found to lie in or close to the nickel 〈00{\=1}〉 rows. These results are not in agreement with recently published dynamical LEED calculations.",

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T1 - Structure analysis of an oxidized nickel (110) surface using low energy ion scattering

AU - Verheij, L. K.

AU - Van Den Berg, J. A.

AU - Armour, D. G.

PY - 1979/6/1

Y1 - 1979/6/1

N2 - Low energy (6 keV) argon and neon ion scattering in the low angle mode (θ = 30°) has been used to investigate changes in the surface structure of a Ni(110) surface caused by the adsorption of oxygen at low exposures (10-6 Torr s). The experimental energy spectra indicate that due to adsorption of oxygen, the interatomic distance in the 〈1̄10〉 direction increases while in the 〈001̄〉 direction this distance seems to decrease. This represents strong evidence that a reconstruction process is taking place during the early stages of oxidation of the Ni(110) face, in which the interatomic distances in the 〈1̄10〉 direction doubles. The oxygen atoms were found to lie in or close to the nickel 〈001̄〉 rows. These results are not in agreement with recently published dynamical LEED calculations.

AB - Low energy (6 keV) argon and neon ion scattering in the low angle mode (θ = 30°) has been used to investigate changes in the surface structure of a Ni(110) surface caused by the adsorption of oxygen at low exposures (10-6 Torr s). The experimental energy spectra indicate that due to adsorption of oxygen, the interatomic distance in the 〈1̄10〉 direction increases while in the 〈001̄〉 direction this distance seems to decrease. This represents strong evidence that a reconstruction process is taking place during the early stages of oxidation of the Ni(110) face, in which the interatomic distances in the 〈1̄10〉 direction doubles. The oxygen atoms were found to lie in or close to the nickel 〈001̄〉 rows. These results are not in agreement with recently published dynamical LEED calculations.

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