Adsorption of elemental S on Si(100)-2x1 surfaces

被引:25
作者
Papageorgopoulos, A
Kamaratos, M
机构
[1] CLARK ATLANTA UNIV,DEPT PHYS,ATLANTA,GA 30314
[2] CLARK ATLANTA UNIV,CTR HIGH PERFORMANCE POLYMERS & CERAM,ATLANTA,GA 30314
[3] UNIV IOANNINA,DEPT PHYS,GR-45110 IOANNINA,GREECE
基金
美国国家航空航天局;
关键词
adsorption kinetics; atom-solid interactions; scattering; diffraction; auger electron spectroscopy; chemisorption; low energy electron diffraction (LEED); low index single crystal surfaces; semiconducting surfaces; silicon; sulphides; surface electronic phenomena; thermal desorption spectroscopy; work function measurements;
D O I
10.1016/0039-6028(95)01161-7
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
We have studied the adsorption of elemental S on Si(100)-2 X 1 surfaces by LEED, AES, TDS, and WF measurements in UHV. The adsorption of S at room temperature causes the surface restoration of the reconstructed Si(100)-2 X 1 substrate to its original bulk-terminated surface, Si(100)-1 X 1. The S adsorbate follows the substrate structures, i.e. it forms initially a (2 X 1) up to 0.5 ML and subsequently a (1 X 1). Above 1 ML, sulfur is imbedded into the Si bulk near the surface. The sticking coefficient of S on Si(100) surface is constant, S = 1, up to 2 ML. Deposition of S at RT up to 1 ML increases the WF of the surface by about 0.30 +/- 0.05 eV. Above 1 ML, as the S is diffused into the Si bulk, the WF decreases, The TDS measurements show that S is desorbed as SiS molecule with a single TD peak near 585 degrees C. This may indicate that the Si-S bond energy is greater than that of Si-Si which may be the dominant cause of the substrate restoration.
引用
收藏
页码:364 / 368
页数:5
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