Photocorrosion of n-GaAs and passivation by Na2S: A comparison of the (100), (110), and (111)B faces

被引:27
作者
Miller, EA
Richmond, GL
机构
[1] UNIV OREGON,DEPT CHEM,EUGENE,OR 97403
[2] UNIV OREGON,INST MAT SCI,EUGENE,OR 97403
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 1997年 / 101卷 / 14期
关键词
D O I
10.1021/jp962852k
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
Photocorrosion of n-GaAs and passivation by Na2S have been studied in a working photoelectrochemical cell as a function of crystal face orientation. Time-resolved photoluminescence studies of the (100), (110), and (111)B faces of n-GaAs show that Na2S provides a similar degree of corrosion protection to the (100) and (110) faces, although the corrosion-induced surface states eventually formed at each interface are separated in energy by similar to 300 meV. Unlike (100) and (110), the (111)B surface is not passivated by Na2S. The high density of intrinsic surface states at the (111)B n-GaAs surface, and the lack of removal of these states by Na2S, pins the Fermi level and prevents trap saturation. X-ray photoelectron spectroscopic studies of the three surfaces before and after Na2S treatment show a significant degree of arsenic sulfide bonding on (100) and (110). The (111)B face shows very little As-S bonding, indicating that formation of interfacial sulfides plays an important role in the reduction of interfacial traps and passivation of the photocorrosion reaction.
引用
收藏
页码:2669 / 2677
页数:9
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