Interaction of H, O2, and H2O with 3C-SiC surfaces

被引:52
作者
Amy, F [1 ]
Chabal, YJ
机构
[1] Princeton Univ, Dept Elect Engn, Princeton, NJ 08544 USA
[2] Rutgers State Univ, Dept Chem, Piscataway, NJ 08855 USA
[3] Agere Syst, Mat Res Dept, Murray Hill, NJ 07974 USA
关键词
D O I
10.1063/1.1602052
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
Infrared absorption spectroscopy studies of Si-dimer-terminated 3C-SiC(100) 3x2 and c4x2 surfaces reveal marked differences between their atomic scale reactivity with H, O-2, and H2O and that of Si(100) surfaces. While atomic hydrogen is well known to passivate dangling bonds on all Si surfaces, H exposure on both 3C-SiC(100) 3x2 and c(4x2) surfaces induces a metallic state instead. Furthermore, hydrogenated 3C-SiC(100) 3x2 surfaces exposed to O-2 clearly show that oxygen atoms are inserted below the top surface without any loss in the H coverage at room temperature. Finally, while H2O decomposes into H and OH on both Si(100) 2x1 and 3C-SiC(100) 3x2, subsequent atomic H exposure induces a metallic state on the latter only, creating a thin oxide strip on the top surface separated by a metallic trough. (C) 2003 American Institute of Physics.
引用
收藏
页码:6201 / 6209
页数:9
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