The structure and crystallization of thin water films on Pt(111)
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Zimbitas, G
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Haq, S
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Univ Liverpool, Suface Sci Res Ctr, Liverpool L69 3BX, Merseyside, EnglandUniv Liverpool, Suface Sci Res Ctr, Liverpool L69 3BX, Merseyside, England
Haq, S
[1
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Hodgson, A
[1
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[1] Univ Liverpool, Suface Sci Res Ctr, Liverpool L69 3BX, Merseyside, England
When water is adsorbed on Pt(111) above 135 K several different ice structures crystallize, depending on the thickness of the ice layer. At low coverage water forms extended islands of ice with a (root 37 X root 37)R25 degrees unit cell, which compresses as the monolayer saturates to form a (root 39 X root 39)R16 degrees structure. The root 39 low-energy electron diffraction (LEED) pattern becomes more intense as the second layer grows, remaining bright for films up of 10-15 layers and then fading and disappearing for films more than ca. 40 layers thick. The ice multilayer consists of an ordered root 39 wetting layer, on which ice grows as a crystalline film which progressively loses its registry to the wetting layer. Ice films more than ca. 50 layers thick develop a hexagonal LEED pattern, the entire film and wetting layer reorienting to form an incommensurate bulk ice. These changes are reflected in the vibrational spectra which show changes in line shape and intensity associated with the different ice structures. Thin amorphous solid water films crystallize to form the same phases observed during growth, implying that these structures are thermodynamically stable and not kinetic phases formed during growth. The change from a root 39 registry to incommensurate bulk ice at ca. 50 layers is associated with a change in crystallization kinetics from nucleation at the Pt(111) interface in thin films to nucleation of incommensurate bulk ice in amorphous solid water films more than 50 layers thick. (c) 2005 American Institute of Physics.
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Univ Liverpool, Surface Sci Res Ctr, Liverpool L69 3BX, Merseyside, EnglandUniv Liverpool, Surface Sci Res Ctr, Liverpool L69 3BX, Merseyside, England
Clay, C
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Haq, S
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Univ Liverpool, Surface Sci Res Ctr, Liverpool L69 3BX, Merseyside, EnglandUniv Liverpool, Surface Sci Res Ctr, Liverpool L69 3BX, Merseyside, England
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Pacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USAPacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USA
Daschbach, JL
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Peden, BM
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Pacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USAPacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USA
Peden, BM
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Smith, RS
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Pacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USAPacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USA
Smith, RS
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Kay, BD
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Pacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USAPacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USA
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Univ Liverpool, Surface Sci Res Ctr, Liverpool L69 3BX, Merseyside, EnglandUniv Liverpool, Surface Sci Res Ctr, Liverpool L69 3BX, Merseyside, England
Clay, C
;
Haq, S
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h-index: 0
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Univ Liverpool, Surface Sci Res Ctr, Liverpool L69 3BX, Merseyside, EnglandUniv Liverpool, Surface Sci Res Ctr, Liverpool L69 3BX, Merseyside, England
机构:
Pacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USAPacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USA
Daschbach, JL
;
Peden, BM
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Pacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USAPacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USA
Peden, BM
;
Smith, RS
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Pacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USAPacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USA
Smith, RS
;
Kay, BD
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Pacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USAPacific NW Natl Lab, Fundamental Sci Directorate, Div Chem Sci, Richland, WA 99352 USA