Influence of the molecular-scale structures of 1-dodecanethiol and 4-methylbenzenethiol self-assembled monolayers on gold nanoparticles adsorption pattern

被引:8
|
作者
Al Mamun, Abdulla He [1 ,2 ]
Yoon, Sangwoon [3 ]
Hahn, Jae Ryang [1 ,2 ]
机构
[1] Chonbuk Natl Univ, Dept Chem & Bioact Mat Sci, Jeonju 561756, South Korea
[2] Chonbuk Natl Univ, Res Inst Phys & Chem, Jeonju 561756, South Korea
[3] Dankook Univ, Dept Chem, Yongin 448701, Gyeonggi, South Korea
关键词
Self-assembled monolayers; Au nanoparticles; Scanning tunneling microscopy; Atomic force microscopy; Hydrophobicity; Adsorption; METAL NANOPARTICLES; ELECTRON-TRANSFER; THIOL MONOLAYERS; ORGANIC-SURFACES; AU(111); CHEMISTRY; SILVER; SHAPE; SIZE; SPECTROSCOPY;
D O I
10.1016/j.jcis.2014.03.043
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
In an effort to understand the effects of the molecular structures of self-assembled monolayers on the patterns formed by immobilized Au nanoparticles (AuNPs), we characterized and compared the morphologies and properties of AuNPs adsorbed onto self-assembled monolayers formed by 1-dodecanethiol (DDT-SAM) or 4-methylbenzenethiol (MBT-SAM) assembled on Au(111) surfaces. The AuNP adsorption pattern on the MBT-SAM surface was well-dispersed and characterized by a low degree of corrugation. By contrast, an aggregated and highly corrugated AuNP pattern was observed on the surface of the DDTSAM. This difference was attributed to the retention or removal of citrate anions present on the AuNPs during adsorption onto the SAM surface. Direct interactions between the AuNPs and the highly corrugated hydrophobic surfaces of the DDT-SAMs could strip the citrate layers from the AuNP surfaces, leading to aggregated adsorption. The water molecules appeared to mediate the adsorption of the AuNPs by reducing the hydrophobicity of the MBT-SAM surface and promoting a more dispersed adsorption configuration. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:83 / 90
页数:8
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