纳米棒
连接器
纳米技术
纳米结构
自组装
材料科学
侧链
合理设计
纳米颗粒
氢键
分子
化学
聚合物
计算机科学
有机化学
复合材料
操作系统
作者
Shu Fen Tan,Utkarsh Anand,Utkur Mirsaidov
出处
期刊:ACS Nano
[American Chemical Society]
日期:2017-01-24
卷期号:11 (2): 1633-1640
被引量:80
标识
DOI:10.1021/acsnano.6b07398
摘要
Nanoparticle (NP) self-assembly has been recognized as an important technological process for forming ordered nanostructures. However, the detailed dynamics of the assembly processes remain poorly understood. Using in situ liquid cell transmission electron microscopy, we describe the assembly modes of gold (Au) nanorods (NRs) in solution mediated by hydrogen bonding between NR-bound cysteamine linker molecules. Our observations reveal that by tuning the linker concentration, two different NR assembly modes can be achieved. These assembly modes proceed via the (1) end-to-end and (2) side-to-side attachment of NRs at low and high linker concentrations in solution, respectively. In addition, our time-resolved observations reveal that the side-to-side NR assemblies can occur through two different pathways: (i) prealigned attachment, where two Au NRs prealign to be parallel prior to assembly, and (ii) postattachment alignment, where two Au NRs first undergo end-to-end attachment and pivot around the attachment point to form the side-to-side assembly. We attributed the observed assembly modes to the distribution of linkers on the NR surfaces and the electrostatic interactions between the NRs. The intermediate steps in the assembly reported here reveal how the shape and surface functionalities of NPs drive their self-assembly, which is important for the rational design of hierarchical nanostructures.
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