Substrate directed self-assembly of anisotropic nanoparticles

被引:8
作者
Patra, Tarak K. [1 ]
Katiyar, Parul [1 ]
Singh, Jayant K. [1 ]
机构
[1] Indian Inst Technol, Dept Chem Engn, Kanpur 208016, Uttar Pradesh, India
关键词
Anisotropic nanoparticle; Self-assembly; Disorder-order transition; Aggregation; Coarse-grained simulation; BUILDING-BLOCKS; GOLD; NANOCRYSTALS; CRYSTALLINE; ORIENTATION; FORCES; SHAPE; GROWTH; ARRAYS;
D O I
10.1016/j.ces.2014.09.023
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
We present a molecular dynamics study on the self assembly of anisotropic nanoparticles triangles and tetrahedrons on a flat surface. We observe ordered and disordered aggregates of nanoparticles depending on the particle particle and surface particle interactions. Anisotropic particles induce directionality in the assembly process. In particular, a cross over from the isotropic (spherical) assembly to the anisotropic (nun spherical) assembly of nanoparticles is identified as their size increases for weak nanoparticle-surface interactions. However, at strong nanoparticle-surface interactions, clusters of nanoparticles grow uniformly on the surface. We present phase diagrams that depict all possible structures of triangles and tetrahedrons depending on their size (L) and the nanoparticle-surface interaction strength (epsilon(ns)). We show a disorder to order transition in the L-epsilon(ns) plane, as L and epsilon(ns) increase. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:16 / 22
页数:7
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