Decomposition reactions of ethanethiol on GaAs (100)

被引:23
作者
Singh, NK [1 ]
Doran, DC [1 ]
机构
[1] Univ New S Wales, Sch Chem, Sydney, NSW 2052, Australia
关键词
Auger electron spectroscopy; chemisorption; gallium arsenide; surface chemical reactions; thermal desorption;
D O I
10.1016/S0039-6028(98)00871-1
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 adsorption and thermal decomposition reactions of ethanethiol on gallium-rich GaAs(100)-(4 x 1) have been investigated using the techniques of Auger electron spectroscopy (AES), low-energy electron diffraction (LEED) and thermal desorption spectroscopy (TDS) in conjunction with deuterium isotope scrambling experiments. Exposures of ethanethiol onto clean GaAs(100) at room temperature to saturation coverage followed by annealing to 750 K forms a p(2 x 2) structure, and AES confirms that this structure is due to a pure sulfur overlayer. Upon adsorption ethanethiol undergoes S-H scission to form surface ethanethiolate and hydrogen species. Recombinative desorption of ethanethiol competes with the decomposition reaction of ethanethiolate via C-S scission to form adsorbed ethyl and sulfur species, and this C-S cleavage occurs below 500 K. On the clean surface, the further reactions of the ethyl species lead to the production of a mixture of products consisting of ethene, ethanol hydrogen and butene, which all desorb below 600 K. Ethene, ethane and hydrogen are formed as a direct result of P-hydride and reductive elimination reactions of the ethyl species, while butene is formed during ethyl coupling reactions on the surface. On a sulfided surface, butane, hydrogen sulfide and diethylsulfide are formed in addition to the product mixture noted above, and all desorb into the gas phase below 600 K. A reaction scheme is proposed to account for the observed desorption products on both the clean and pre-sulfided GaAs(100) surfaces. (C) 1999 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:50 / 64
页数:15
相关论文
共 41 条
[1]   THE MECHANISM OF THE DECOMPOSITION OF METHANETHIOL ON FE(100) [J].
ALBERT, MR ;
LU, JP ;
BERNASEK, SL ;
CAMERON, SD ;
GLAND, JL .
SURFACE SCIENCE, 1988, 206 (03) :348-364
[2]  
Aylward G. H., 1994, SI Chemical Data, V3rd
[3]   FORMATION OF SUPER AS-RICH GAAS(100) SURFACES BY HIGH-TEMPERATURE EXPOSURE TO ARSINE [J].
BANSE, BA ;
CREIGHTON, JR .
APPLIED PHYSICS LETTERS, 1992, 60 (07) :856-858
[4]   Role of intermolecular interactions in determining structure and reactivity on surfaces: Benzenethiol on Rh(111) [J].
Bol, CWJ ;
Friend, CM ;
Xu, X .
LANGMUIR, 1996, 12 (25) :6083-6090
[5]  
BOLZAN AB, 1995, THESIS U NEW S WAL S
[6]   METHANETHIOL DECOMPOSITION ON NI(100) [J].
CASTRO, ME ;
AHKTER, S ;
GOLCHET, A ;
WHITE, JM ;
SAHIN, T .
LANGMUIR, 1991, 7 (01) :126-133
[7]   Reactions of methanethiol on cobalt-covered Mo(110) [J].
Chen, DA ;
Friend, CM ;
Xu, H .
LANGMUIR, 1996, 12 (06) :1528-1534
[8]   Coadsorption of ethanethiol with sulfur, oxygen, and water on the Fe(100) surface [J].
Cheng, LC ;
Bocarsly, AB ;
Bernasek, SL ;
Ramanarayanan, TA .
LANGMUIR, 1996, 12 (02) :392-401
[9]   INTERACTION OF ALKANETHIOLS WITH SINGLE-CRYSTAL IRON - THE LOW-TEMPERATURE DECOMPOSITION OF ETHANETHIOL ON THE FE(100) SURFACE [J].
CHENG, LC ;
BOCARSLY, AB ;
BERNASEK, SL ;
RAMANARAYANAN, TA .
LANGMUIR, 1994, 10 (12) :4542-4550
[10]   Adsorption state of hydrogen sulfide on the GaAs(001)-(4x2) surface [J].
Chung, CH ;
Yi, SI ;
Weinberg, WH .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A, 1997, 15 (03) :1163-1167