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金纳米粒子在纳米图案化表面上的 DNA 导向自组装:将单个纳米粒子精确地放置在规则的阵列中。

DNA-directed self-assembly of gold nanoparticles onto nanopatterned surfaces: controlled placement of individual nanoparticles into regular arrays.

机构信息

School of Chemistry, Monash University, Wellington Road, Clayton, VIC 3800, Australia.

出版信息

ACS Nano. 2010 Oct 26;4(10):6153-61. doi: 10.1021/nn101431k.

Abstract

A method for the templated DNA-directed self-assembly of individual gold nanoparticles (AuNPs) into discrete nanostructures is described. The templating nanostructures consisted of a linear configuration of six metal dots with a center-to-center dot distance of 55 nm, fabricated by means of electron beam lithography. The 40 nm DNA-capped AuNPs were immobilized onto this templating nanostructure to produce a linear configuration of six adjacent AuNPs. The geometry of the templating nanostructure was found to be critically important for the successful direction of a single nanoparticle onto individual adsorption sites. For optimized template structures the immobilization efficiency of nanoparticles onto the individual adsorption sites was found to be 80%. The nonspecific association of nanoparticles with specifically adsorbed nanoparticles and the between adsorption of nanoparticles, bridging two individual adsorption sites, were the two main defects observed in the immobilized assemblies. Less than 1% of all surface confined AuNPs adsorbed nonspecifically in the areas between the self-assembled regular arrays.

摘要

描述了一种在模板指导下将单个金纳米粒子(AuNPs)自组装成离散纳米结构的方法。模板纳米结构由通过电子束光刻制成的具有 55nm 中心到中心的点距离的六个金属点的线性配置组成。40nm 的 DNA 封端 AuNPs 被固定到这个模板纳米结构上,以产生六个相邻 AuNP 的线性配置。发现模板纳米结构的几何形状对于成功地将单个纳米粒子引导到单个吸附位点上至关重要。对于优化的模板结构,纳米粒子在单个吸附位点上的固定效率被发现达到 80%。在固定组装体中观察到的两个主要缺陷是纳米粒子与特异性吸附的纳米粒子的非特异性缔合,以及桥接两个单独吸附位点的纳米粒子之间的吸附。在自组装的规则阵列之间的区域中,小于所有表面受限 AuNPs 的 1%非特异性吸附。

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