Observation of ionic desorption channels in cluster-induced desorption of alkali halides - Influence of surface electronic properties and surface configuration

被引：13
|
作者：
Lee, B. -J. [1 ]
Gebhardt, C. R. [2 ]
Schroeder, H. [3 ]
Kompa, K. L. [3 ]
Duerr, M. [1 ]
机构：
[1] Hsch Esslingen, Fak Angew Nat Wissensch, D-73728 Esslingen, Germany
[2] Bruker Daltonik GmbH, D-28359 Bremen, Germany
[3] Max Planck Inst Quantum Opt, D-85748 Garching, Germany
来源：
CHEMICAL PHYSICS LETTERS | 2013年 / 556卷
关键词：
MASS-SPECTROMETRY; MOLECULES; ADSORPTION; POTASSIUM; HYDRATION; DYNAMICS;
D O I：
10.1016/j.cplett.2012.11.031
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：
Desorption of alkali halides upon collision of neutral SO2 clusters on Au and SiO2 surfaces was investigated. For desorption of halogen species X, an ionic desorption channel of the form of (SO2)(n)X- was identified at room temperature on both surfaces. Temperature programmed redistribution of the surface configuration suppresses this desorption channel. Alkali species are desorbed as (SO2)(n)M+; however, on Au surfaces the signal is accompanied by a (SO2)(n)SO2- signal of the same intensity. No such (SO2)(n)SO2- signal of similar strength was observed for desorption from SiO2. The difference is attributed to the different electronic structure of the two substrates. (C) 2012 Elsevier B. V. All rights reserved.
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页码：77 / 81
页数：5
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