Nanopatterning Si(111) surfaces as a selective surface-chemistry route

被引:0
|
作者
Michalak D.J. [1 ,4 ,5 ]
Amy S.R. [1 ,4 ]
Aureau D. [2 ]
Dai M. [1 ]
Estève A. [3 ]
Chabal Y.J. [2 ]
机构
[1] Department of Chemistry and Chemical Biology, Rutgers University, Piscataway
[2] Department of Materials Science and Engineering, University of Texas at Dallas, Richardson
[3] CNRS-Laboratoire d'Analyse et d'Architecture des Systèmes, University of Toulouse
[4] Components Research, Intel Corporation, Hillsboro
[5] Global Technology Center, Air Products and Chemicals, Allentown
基金
美国国家科学基金会;
关键词
D O I
10.1038/nmat2611
中图分类号
学科分类号
摘要
Using wet-chemical self-assembly, we demonstrate that standard surface reactions can be markedly altered. Although HF etching of Si surfaces is known to produce H-terminated surfaces, we show that up to ∼30% of a monolayer of stable Si-F bonds can be formed on atomically smooth Si(111) surfaces on HF reaction, when chemically isolated Si atoms are the target of the reaction. Similarly, ∼30% Si-OH termination can be achieved by immersion of the partially covered F-Si(111) surface in water without oxidation of the underlying Si substrate. Such reactions are possible when H-terminated (111)-oriented Si surfaces are initially uniformly patterned with methoxy groups. These findings are contrary to the knowledge built over the past twenty years and highlight the importance of steric interactions at surfaces and the possibility to stabilize products at surfaces that cannot be obtained on chemically homogeneous surfaces.
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页码:266 / 271
页数:5
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