| Literature DB >> 26509492 |
Xin Qi1, Tonnam Balankura1, Ya Zhou1, Kristen A Fichthorn1.
Abstract
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.Entities:
Keywords: Ag; Nanocrystal; density functional theory; molecular dynamics; polyvinylpyrrolidone
Year: 2015 PMID: 26509492 DOI: 10.1021/acs.nanolett.5b04204
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189