Novel field-induced gray-level selective patterning of self-assembled aminosilane monolayer on SiO2 surfaces by scanning probe bond-breaking lithography

Chia Hao Wu*, Ten Min Lee, Jeng-Tzong Sheu, Tien-Sheng Chao

*Corresponding author for this work

研究成果: Article同行評審

1 引文 斯高帕斯(Scopus)

摘要

We demonstrated a successful strategy for combining the straightforward scanning probe chemical bond-breaking lithography and selfassembly monolayer (SAM) techniques for constructing nanoscale architectural structures of gold nanoparticles (AuNPs) onto modified SiO2 surfaces. The hydroxyl-terminated surface of the sample substrate was modified by silanization with N-(2-aminoethyl)-3-aminopropyltrimethoxysilane (AEAPTMS) molecules. Local-field-induced scanning probe bond-breaking lithography is adopted to selectively decompose the chemical bonds of AEAPTMS SAMs on aminosilane-modified SiO2 surfaces. From the experiments, a tip bias of less than 4.5V cannot effectively decompose chemical bonds of AEAPTMS SAMs. Gray-level selectively patterned pictures were successfully observed on a modified 2.5-nm-thick SiO2 surface by applying dc voltage (2.5-5.5 V) between the atomic force microscopy (AFM) conductive tip and the SiO2 surface under ambient conditions. After the scanning probe selective decomposition of AEAPTMS SAMs, AuNPs with negative-charged citrate surfaces were selectively anchored in the selective patterning region via Coulomb electrostatic force. With proper control, it is considered that this novel technique can be applicable to the generation of various nanofabricated devices.

原文English
文章編號04C133
期刊Japanese Journal of Applied Physics
48
發行號4 PART 2
DOIs
出版狀態Published - 1 四月 2009

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