Molecular self-assembly at bare semiconductor surfaces: Investigation of the chemical and electronic properties of the alkanethiolate-GaAs(001) interface

被引:77
作者
McGuiness, Christine L.
Shaporenko, Andrey
Zharnikov, Michael
Walker, Amy V.
Allara, David L.
机构
[1] Penn State Univ, Dept Chem, University Pk, PA 16801 USA
[2] Penn State Univ, Dept Mat Sci, University Pk, PA 16801 USA
[3] Heidelberg Univ, Angew Phys Chem, D-69120 Heidelberg, Germany
[4] Washington Univ, Dept Chem, St Louis, MO 63130 USA
关键词
D O I
10.1021/jp065173a
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
High-resolution X-ray photoelectron spectroscopy (HRXPS), time-of-flight secondary ion mass spectrometry (ToF-SIMS), and Raman scattering have been used to characterize the bonding and electronic properties of the interfaces formed by ambient-temperature, solution self-assembly of octadecanethiol and dodecanethiol under oxygen-free conditions on GaAs(001) surfaces. The combination of HRXPS and ToF-SIMS shows that both monolayers form direct S-[GaAs] attachment to the bare substrate with dominant As-S bonding and some fraction of Ga-S bonding, but the densely packed octadecanethiolate self-assembled monolayers (SAMs) are significantly more effective in protecting the interface from oxide regrowth compared to the less dense dodecanethiolate SAMs. Raman scattering measurements of the GaAs LO phonon modes indicate that the formation of these direct, oxide-free S-[GaAs] interfaces does not induce any significant changes in the GaAs surface electronic states, whereas control experiments with inorganic sulfide treatment does indicate a significant reduction in the surface traps, consistent with earlier reports. Overall these experiments show that the formation of direct alkane-S-[GaAs(001)] interfaces of high quality provides a method to passivate the GaAs surface against oxide regrowth but does not necessarily lead to changes in the surface electronic states.
引用
收藏
页码:4226 / 4234
页数:9
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