Common fingerprint of hydroxylated non-polar steps on MgO smoke and MgO films

被引:12
作者
Savio, L. [1 ]
Smerieri, M. [1 ,2 ]
Orzelli, A. [2 ]
Vattuone, L. [1 ,2 ]
Rocca, M. [1 ,2 ]
Finocchi, F. [3 ]
Jupille, J. [3 ]
机构
[1] IMEM CNR, I-16146 Genoa, Italy
[2] Univ Genoa, Dipartimento Fis, I-16146 Genoa, Italy
[3] Univ Paris 06, UPMC, Inst Nanosci Paris, CNRS UMR 7588, F-75015 Paris, France
关键词
Magnesium oxide; Hydroxylation; Vibrational spectroscopy; Scanning tunnelling microscopy; Density functional theory; MgO smoke; MgO film; ENERGY;
D O I
10.1016/j.susc.2009.11.013
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The infrared spectra of MgO smoke exposed to water are compared to high-resolution electron energy loss spectra (HREELS) of hydroxylated ultrathin MgO(1 0 0)/Ag(1 0 0) films. Very similar bands are observed at 3458-3480 cm(-1) and 3710-3714 cm(-1). On the basis of first principle calculations, these bands are interpreted as the stretching modes of the two distinct OH groups that are formed at monatomic steps parallel to < 1 0 0 > crystallographic directions. The lower frequency band is due to H adsorbed on O at the step edge, while the higher frequency one originates from OH groups that are twofold coordinated with Mg. Consistently, scanning tunnelling microscopy images of MgO films, prepared in similar conditions as during the HREELS experiments, show that the MgO/Ag(1 0 0) island edges are mainly nonpolar, i.e. oriented along the < 1 0 0 > direction. In spite of that, a minor contribution to the OH-stretch intensity from hydroxylated polar < 1 0 0 > steps cannot be excluded; for such geometry density functional theory predicts indeed a single OH species with a vibrational frequency very close to the high-frequency band of OH adsorbed at < 1 0 0 > steps. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:252 / 257
页数:6
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