Enhanced local oxidation of silicon using a conducting atomic force microscope in water

被引:4
|
作者
Hilton, A. M. [1 ]
Jacobson, K. W. [1 ]
Lynch, B. P. [1 ]
Simpson, G. J. [1 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
来源
基金
美国国家科学基金会;
关键词
D O I
10.1116/1.2819256
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
A new mechanism for direct-write surface scanning probe lithography is considered based on electrodynamic cavitation in a true liquid environment. Oxide layers grown on Si/SiO2/H2O and Si/SiO2/Au/H2O interfaces reached maximum heights of 130 and 690 nm, respectively. These structures represent a full order of magnitude increase in height over oxides grown in air under similar voltages and time durations, suggesting a unique reaction mechanism. Time-dependent studies indicated that oxide structures generated in water grew by discrete intervals and occasionally grew at a significant distance from the tip, effects that have not been previously reported. The possibility of electrodynamic cavitation-assisting silicon oxide growth under aqueous conditions is considered, potentially opening up opportunities for formation of nanoscale surface structures based on largely underutilized cavitation-induced (e.g., sonochemical) reactions. (C) 2008 American Vacuum Society.
引用
收藏
页码:47 / 51
页数:5
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