Ling Xing, Zhu Xin, Zhang Jin, Zhu Tao, Liu Manhong, Tong Lianming, Liu Zhongfan
College of Chemistry and Molecular Engineering, Center for Nanoscale Science and Technology (CNST), Peking University, Beijing 100871, China.
J Phys Chem B. 2005 Feb 24;109(7):2657-65. doi: 10.1021/jp0456077.
This paper describes a rational approach for reproducibly patterning single Au nanoparticles, 15-20-nm diameter, on silicon wafer substrates. The approach uses scanning probe oxidation (SPO) to pattern silicon oxide nanodomain arrays on silicon substrates modified with octadecyltrimethoxysilane (OTS). It was usually found using aminopropyltrimethoxysilane (APS) that Au nanoparticles only assembled at the domain boundaries probably because of asymmetrically distributed hydroxyl groups. To generate uniformly distributed hydroxyl groups on oxide domains, we employed a two-step treatment to etch and oxidize the substrate. With this treatment, oxide domains consistently attached Au nanoparticles to maximum capacity. Single Au nanoparticles were readily patterned by fabricating oxide nanodomains with a diameter below 30 nm. We also investigated the deposition of APS on OTS monolayers, which resulted in the assembly of Au nanoparticles outside of the oxide domains, and proposed two alternative methods to inhibit it.
本文描述了一种在硅片衬底上可重复地对直径为15 - 20纳米的单个金纳米颗粒进行图案化的合理方法。该方法利用扫描探针氧化(SPO)在经十八烷基三甲氧基硅烷(OTS)修饰的硅衬底上对氧化硅纳米域阵列进行图案化。通常发现,使用氨丙基三甲氧基硅烷(APS)时,金纳米颗粒仅在域边界处组装,这可能是由于羟基分布不对称所致。为了在氧化物域上产生均匀分布的羟基,我们采用了两步处理来蚀刻和氧化衬底。通过这种处理,氧化物域始终能以最大容量附着金纳米颗粒。通过制造直径小于30纳米的氧化物纳米域,可轻松对单个金纳米颗粒进行图案化。我们还研究了APS在OTS单分子层上的沉积情况,这导致金纳米颗粒在氧化物域外组装,并提出了两种抑制这种情况的替代方法。