Self-assembly of gold nanoparticles on functional organic molecular crystals

被引:3
|
作者
Trabattoni, Silvia [1 ]
Moret, Massimo [1 ]
Miozzo, Luciano [1 ]
Campione, Marcello [2 ]
机构
[1] Univ Milano Bicocca, Dept Mat Sci, I-20125 Milan, Italy
[2] Univ Milano Bicocca, Dept Geol Sci & Geotechnol, I-20126 Milan, Italy
关键词
Gold nanoparticle; Organic crystal; Atomic force microscopy; Fluid cell; ENERGY-DISSIPATION; ORDER FORMATION; FORCE; METAL; TEMPERATURE; ADSORPTION; DEPENDENCE; SUBSTRATE; DYNAMICS; FILM;
D O I
10.1016/j.jcis.2011.04.102
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The utilization of metal nanoparticles (NPs) to fabricate metal electrodes under mild conditions is one of the most studied topic in recent years. In this work, colloidal Au NPs were deposited on two isostructural molecular crystals, namely 1,2,3,4-tetrafluoro-7-thiomethyl-acridine (MeSAcr) and 1,2,3,4-tetrafluoro-7-methoxy-acridine (MeOAcr), exposing S atoms and O atoms, respectively, at their largest crystal faces. The depositions were carried out mainly by drop casting under ambient conditions, increasing the contact time from 1 to 120 min, and the samples were then analyzed by atomic force microscopy (AFM) to evaluate the coverage. Thanks to the affinity between S and Au atoms, Au NPs are observed to adhere on the MeSAcr surface within 1-min contact time, whereas at least 1 h is required to find NPs on the MeOAcr surface. NP adsorption is also affected by the substrate surface morphology; indeed, step edges represent preferential adsorption sites even in the absence of Au-S interaction. Experiments under different conditions were performed to maximize the coverage on MeSAcr, reaching values up to 13%. AFM equipped with fluid cell was also employed to simultaneously depositing and imaging NPs, achieving a better understanding of the adsorption mechanism. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:422 / 429
页数:8
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