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Spatially Controlled Functionalization and Chemical Manipulation to Fabricate Two-Dimensional Arrays of Gold Nanoparticles onto Indium Tin Oxide

机译:空间控制的功能化和化学处理,以在氧化铟锡上制造金纳米粒子的二维阵列

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摘要

We demonstrate the formation of two-dimensional (2D) arrays of gold nanoparticles (AuNPs) by controlled functionalization in a regular linear fashion, on the basis of the self-assembly and vacuum ultraviolet (VUV) lithography approaches. An octadecyltrimethoxysilane (ODS) monolayer, self-assembled on an indium tin oxide (ITO) surface, was exposed to VUV light (172 nm) through a photomask to construct the linear pattern by photodegradation of the ODS monolayer. Subsequently, an aminopropyltriethoxysilane (APS) monolayer was deposited on VUV-exposed sites by chemical vapor deposition. The immobilization of AuNPs on amino-terminated sites is due to the electrostatic attraction between citrate-stabilized AuNPs and amino groups of the APS monolayer, while the methyl-terminated sites remain unexposed. The structural organization of AuNPs in an alternating linear fashion was demonstrated by scanning electron microscope (SEM) analysis. The X-ray photoelectron microscopy (XPS) measurements were performed to probe the self-assembly of ODS, the APS monolayer, photopatterning and AuNPs immobilization.
机译:我们展示了在自组装和真空紫外(VUV)光刻方法的基础上,以规则的线性方式通过受控功能化形成了金纳米颗粒(AuNPs)的二维(2D)阵列。自组装在氧化铟锡(ITO)表面上的十八烷基三甲氧基硅烷(ODS)单层通过光掩模暴露于VUV光(172 nm),以通过ODS单层的光降解来构建线性图案。随后,通过化学气相沉积将氨丙基三乙氧基硅烷(APS)单层沉积在暴露于VUV的位置上。 AuNPs在氨基末端位点上的固定化是由于柠檬酸盐稳定的AuNPs与APS单层氨基之间的静电吸引,而甲基末端位点仍未暴露。通过扫描电子显微镜(SEM)分析证明了AuNPs以交替线性方式的结构组织。进行X射线光电子显微镜(XPS)测量以探测ODS的自组装,APS单层,光图案化和AuNPs固定化。

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