Kr and Xe on NaCl(1 0 0): Pure phases and their miscibility

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OriginalspracheEnglisch
Seiten (von - bis)71-85
Seitenumfang15
FachzeitschriftSurface Science
Jahrgang473
Ausgabenummer1-2
PublikationsstatusVeröffentlicht - 9 Feb. 2001

Abstract

Using LEED spot profile analysis (SPA-LEED) and thermal programmed desorption spectroscopy (TDS), the pure Kr/NaCl(1 0 0) system and its mixture with Xe has been studied. As substrate thin epitaxial NaCl films on a Ge(1 0 0) substrate have been used. Kr in the monolayer (MC) regime forms a faint (2×1)pmg structure with glide plane symmetry, whereas the second layer forms a quadratic lattice with a lattice constant close to the Kr bulk value. From the phase diagram for Kr condensation into the first and second monolayer heats of condensation of 9.5±2 and 9.0±2 kJ/mol have been derived, respectively. These are significantly lower than those obtained from TDS. Mixtures of Kr with preadsorbed Xe have been studied for preadsorbed Xe coverages 0≤ΘXe≤3 ML under isobaric Kr pressures between 10-7≤pKr≤10-6 mbar and at surface temperatures between 35≤T≤60 K. Emphasis is put on investigations of the first monolayer. The phase transition of Kr condensation into the first monolayer is shifted to higher transition temperature and broadens for the mixtures. Whereas no new ordered structures have been observed compared with the pure Xe and Kr systems, atomic mixture in the first layer is confirmed by the observation of a continuously varying average lattice constant in one direction between the (2×1)pmg and the distorted hexagonal structure of Xe. A miscibility gap depending on T, pKr and ΘXe is found. At Tc of Kr condensation in the first layer, the solubilities are sKr to approximately 0.25 and sXe to approximately 0.3. For pKr>5×10-7 mbar the miscibility gap closes prior to the transition to a Kr three-dimensional layer. The mixture of Kr into the first layer of Xe is even observed for preadsorbed Xe coverages above one monolayer.

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Kr and Xe on NaCl(1 0 0): Pure phases and their miscibility. / Budde, K.; Schimmelpfennig, J.; Eichmann, M. et al.
in: Surface Science, Jahrgang 473, Nr. 1-2, 09.02.2001, S. 71-85.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Budde, K, Schimmelpfennig, J, Eichmann, M, Ernst, W & Pfnür, H 2001, 'Kr and Xe on NaCl(1 0 0): Pure phases and their miscibility', Surface Science, Jg. 473, Nr. 1-2, S. 71-85. https://doi.org/10.1016/S0039-6028(00)00955-9
Budde K, Schimmelpfennig J, Eichmann M, Ernst W, Pfnür H. Kr and Xe on NaCl(1 0 0): Pure phases and their miscibility. Surface Science. 2001 Feb 9;473(1-2):71-85. doi: 10.1016/S0039-6028(00)00955-9
Budde, K. ; Schimmelpfennig, J. ; Eichmann, M. et al. / Kr and Xe on NaCl(1 0 0) : Pure phases and their miscibility. in: Surface Science. 2001 ; Jahrgang 473, Nr. 1-2. S. 71-85.
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title = "Kr and Xe on NaCl(1 0 0): Pure phases and their miscibility",
abstract = "Using LEED spot profile analysis (SPA-LEED) and thermal programmed desorption spectroscopy (TDS), the pure Kr/NaCl(1 0 0) system and its mixture with Xe has been studied. As substrate thin epitaxial NaCl films on a Ge(1 0 0) substrate have been used. Kr in the monolayer (MC) regime forms a faint (2×1)pmg structure with glide plane symmetry, whereas the second layer forms a quadratic lattice with a lattice constant close to the Kr bulk value. From the phase diagram for Kr condensation into the first and second monolayer heats of condensation of 9.5±2 and 9.0±2 kJ/mol have been derived, respectively. These are significantly lower than those obtained from TDS. Mixtures of Kr with preadsorbed Xe have been studied for preadsorbed Xe coverages 0≤ΘXe≤3 ML under isobaric Kr pressures between 10-7≤pKr≤10-6 mbar and at surface temperatures between 35≤T≤60 K. Emphasis is put on investigations of the first monolayer. The phase transition of Kr condensation into the first monolayer is shifted to higher transition temperature and broadens for the mixtures. Whereas no new ordered structures have been observed compared with the pure Xe and Kr systems, atomic mixture in the first layer is confirmed by the observation of a continuously varying average lattice constant in one direction between the (2×1)pmg and the distorted hexagonal structure of Xe. A miscibility gap depending on T, pKr and ΘXe is found. At Tc of Kr condensation in the first layer, the solubilities are sKr to approximately 0.25 and sXe to approximately 0.3. For pKr>5×10-7 mbar the miscibility gap closes prior to the transition to a Kr three-dimensional layer. The mixture of Kr into the first layer of Xe is even observed for preadsorbed Xe coverages above one monolayer.",
author = "K. Budde and J. Schimmelpfennig and M. Eichmann and W. Ernst and Herbert Pfn{\"u}r",
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TY - JOUR

T1 - Kr and Xe on NaCl(1 0 0)

T2 - Pure phases and their miscibility

AU - Budde, K.

AU - Schimmelpfennig, J.

AU - Eichmann, M.

AU - Ernst, W.

AU - Pfnür, Herbert

N1 - Funding information: This work was supported by the Deutsche Forschungsgemeinschaft through Forschergruppe “Adsorbatwechselwirkungen an Ionenkristallen und Metallen”.

PY - 2001/2/9

Y1 - 2001/2/9

N2 - Using LEED spot profile analysis (SPA-LEED) and thermal programmed desorption spectroscopy (TDS), the pure Kr/NaCl(1 0 0) system and its mixture with Xe has been studied. As substrate thin epitaxial NaCl films on a Ge(1 0 0) substrate have been used. Kr in the monolayer (MC) regime forms a faint (2×1)pmg structure with glide plane symmetry, whereas the second layer forms a quadratic lattice with a lattice constant close to the Kr bulk value. From the phase diagram for Kr condensation into the first and second monolayer heats of condensation of 9.5±2 and 9.0±2 kJ/mol have been derived, respectively. These are significantly lower than those obtained from TDS. Mixtures of Kr with preadsorbed Xe have been studied for preadsorbed Xe coverages 0≤ΘXe≤3 ML under isobaric Kr pressures between 10-7≤pKr≤10-6 mbar and at surface temperatures between 35≤T≤60 K. Emphasis is put on investigations of the first monolayer. The phase transition of Kr condensation into the first monolayer is shifted to higher transition temperature and broadens for the mixtures. Whereas no new ordered structures have been observed compared with the pure Xe and Kr systems, atomic mixture in the first layer is confirmed by the observation of a continuously varying average lattice constant in one direction between the (2×1)pmg and the distorted hexagonal structure of Xe. A miscibility gap depending on T, pKr and ΘXe is found. At Tc of Kr condensation in the first layer, the solubilities are sKr to approximately 0.25 and sXe to approximately 0.3. For pKr>5×10-7 mbar the miscibility gap closes prior to the transition to a Kr three-dimensional layer. The mixture of Kr into the first layer of Xe is even observed for preadsorbed Xe coverages above one monolayer.

AB - Using LEED spot profile analysis (SPA-LEED) and thermal programmed desorption spectroscopy (TDS), the pure Kr/NaCl(1 0 0) system and its mixture with Xe has been studied. As substrate thin epitaxial NaCl films on a Ge(1 0 0) substrate have been used. Kr in the monolayer (MC) regime forms a faint (2×1)pmg structure with glide plane symmetry, whereas the second layer forms a quadratic lattice with a lattice constant close to the Kr bulk value. From the phase diagram for Kr condensation into the first and second monolayer heats of condensation of 9.5±2 and 9.0±2 kJ/mol have been derived, respectively. These are significantly lower than those obtained from TDS. Mixtures of Kr with preadsorbed Xe have been studied for preadsorbed Xe coverages 0≤ΘXe≤3 ML under isobaric Kr pressures between 10-7≤pKr≤10-6 mbar and at surface temperatures between 35≤T≤60 K. Emphasis is put on investigations of the first monolayer. The phase transition of Kr condensation into the first monolayer is shifted to higher transition temperature and broadens for the mixtures. Whereas no new ordered structures have been observed compared with the pure Xe and Kr systems, atomic mixture in the first layer is confirmed by the observation of a continuously varying average lattice constant in one direction between the (2×1)pmg and the distorted hexagonal structure of Xe. A miscibility gap depending on T, pKr and ΘXe is found. At Tc of Kr condensation in the first layer, the solubilities are sKr to approximately 0.25 and sXe to approximately 0.3. For pKr>5×10-7 mbar the miscibility gap closes prior to the transition to a Kr three-dimensional layer. The mixture of Kr into the first layer of Xe is even observed for preadsorbed Xe coverages above one monolayer.

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U2 - 10.1016/S0039-6028(00)00955-9

DO - 10.1016/S0039-6028(00)00955-9

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