Growth Mechanism of Five-Fold Twinned Ag Nanowires from Multiscale Theory and Simulations

被引:40
作者
Qi, Xin [1 ]
Chen, Zihao [1 ]
Yan, Tianyu [1 ]
Fichthorn, Kristen A. [1 ,2 ]
机构
[1] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Phys, University Pk, PA 16802 USA
关键词
nanocrystal; nanowire; molecular dynamics; kinetics; growth; Markov chain; UNIFORM SILVER NANOWIRES; MICROSCOPIC ORIGIN; SURFACES INSIGHT; SHAPE EVOLUTION; DYNAMICS; POLYVINYLPYRROLIDONE; ALGORITHMS; PHASE;
D O I
10.1021/acsnano.9b00820
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Five-fold twinned metal nanowires can be 400 synthesized with high aspect ratios via solution-phase methods. The origins of their anisotropic growth, however, are poorly understood. We combine atomic-scale, mesoscale, and continuum theoretical methods to predict growth morphologies of Ag nanowires from seeds and to demonstrate that high aspect ratio nanowires can originate from anisotropic surface diffusion induced by the strained nanowire structure. Nanowire seeds are similar to Marks decahedra, with {111} "notches" that accelerate diffusion along the nanowire axis to facilitate one-dimensional growth. The strain distribution on the {111} facets induces heterogeneous atom aggregation and leads to atom trapping at the nanowire ends. We predict that decahedral Ag seeds can grow to become nanowires with aspect ratios in the experimental range. Our studies show that there is a complex interplay between atom deposition, diffusion, seed architecture, and nanowire aspect ratio that could be manipulated experimentally to achieve controlled nanowire syntheses.
引用
收藏
页码:4647 / 4656
页数:10
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