Self-assembly of large-scale crack-free gold nanoparticle films using a 'drain-to-deposit' strategy

被引:21
作者
Yang, Guang [1 ,2 ]
Hallinan, Daniel T., Jr. [1 ,2 ]
机构
[1] Florida State Univ, Aeroprop Mechatron & Energy Ctr, 2003 Levy Ave, Tallahassee, FL 32310 USA
[2] Florida State Univ, Florida A&M Univ, Coll Engn, Dept Chem & Biomed Engn, 2525 Pottsdamer St, Tallahassee, FL 32310 USA
基金
美国国家科学基金会;
关键词
gold nanoparticle; monolayer; superlattice order; electron microscopy; surface plasmon resonance; surface enhance Raman spectroscopy; GISAXS; ENHANCED RAMAN-SCATTERING; PLASMON RESONANCE; SIZE; SUPERLATTICES; MONOLAYERS; ARRAYS;
D O I
10.1088/0957-4484/27/22/225604
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Gold nanoparticles are widely studied due to the ease of controlled synthesis, facile surface modification, and interesting physical properties. However, a technique for depositing large-area, crack-free monolayers on solid substrates is lacking. Herein is presented a method for accomplishing this. Spherical gold nanoparticles were synthesized as an aqueous dispersion. Assembly into monolayers and ligand exchange occurred simultaneously at an organic/aqueous interface. Then the monolayer film was deposited onto arbitrary solid substrates by slowly pumping out the lower, aqueous phase. This allowed the monolayer film (and liquid-liquid interface) to descend without significant disturbance, eventually reaching substrates contained in the aqueous phase. The resulting macroscopic quality of the films was found to be superior to films transferred by Langmuir techniques. The surface plasmon resonance and Raman enhancement of the films were evaluated and found to be uniform across the surface of each film.
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页数:10
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