聚乙烯吡咯烷酮
纳米晶
纳米结构
材料科学
纳米技术
乙二醇
胶体
化学工程
动能
化学物理
结晶学
化学
高分子化学
物理
量子力学
工程类
作者
Xin Qi,Tonnam Balankura,Ya Zhou,Kristen A. Fichthorn
出处
期刊:Nano Letters
[American Chemical Society]
日期:2015-11-02
卷期号:15 (11): 7711-7717
被引量:105
标识
DOI:10.1021/acs.nanolett.5b04204
摘要
The importance of structure-directing agents (SDAs) in the shape-selective synthesis of colloidal nanostructures has been well documented. However, the mechanisms by which SDAs actuate shape control are poorly understood. In the polyvinylpyrrolidone (PVP)-mediated growth of {100}-faceted Ag nanocrystals, this capability has been attributed to preferential binding of PVP to Ag(100). We use molecular dynamics simulations to probe the mechanisms by which Ag atoms add to Ag(100) and Ag(111) in ethylene glycol solution with PVP. We find that PVP induces kinetic Ag nanocrystal shapes by regulating the relative Ag fluxes to these facets. Stronger PVP binding to Ag(100) leads to a larger Ag flux to Ag(111) and cubic nanostructures through two mechanisms: enhanced Ag trapping by more extended PVP films on Ag(111) and a reduced free-energy barrier for Ag to cross lower-density films on Ag(111). These flux-regulating capabilities depend on PVP concentration and chain length, consistent with experiment.
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