Interaction of methanol and water on MgO(100) studied by ultraviolet photoelectron and metastable impact electron spectroscopies

被引：29

作者：

Günster, J ^{[1
]}

Liu, G ^{[1
]}

Stultz, J ^{[1
]}

Goodman, DW ^{[1
]}

机构：

[1] Texas A&M Univ, Dept Chem, College Stn, TX 77842 USA

来源：

JOURNAL OF CHEMICAL PHYSICS | 1999年 / 110卷 / 05期

关键词：

D O I：

10.1063/1.477962

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 coadsorption of methanol (CH3OH) and water (D2O) on the MgO(100)/Mo(100) surface at 100 K has been studied by metastable impact electron spectroscopy (MIES), ultraviolet photoelectron spectroscopy [UPS (HeI)], and by thermal programmed desorption (TPD). Methanol wets the MgO surface and adsorbs nondissociatively within the first monolayer with the hydroxyl group oriented toward the substrate. In coadsorption experiments, methanol wets a water precovered MgO surface; however, adding water to a methanol precovered MgO surface does not yield a water-only surface. Essentially, a constant fraction of the preadsorbed methanol remains within the topmost surface layer during the buildup of the water multilayer. Temperature-dependent measurements show that the adsorption and desorption dynamics of both water and methanol are governed by intermolecular interactions rather than adsorbate-substrate interactions. (C) 1999 American Institute of Physics. [S0021-9606(99)70505-2].

引用

页码：2558 / 2565

页数：8

共 37 条

[11] Electron spectroscopy using metastable atoms as probes for solid surfaces [J].