Toward Dynamic Control over TiO2 Nanocrystal Monolayer-by-Monolayer Film Formation by Electrophoretic Deposition in Nonpolar Solvents

被引:25
作者
Gonzalo-Juan, I. [1 ,2 ]
Krejci, Alex J. [1 ,2 ]
Dickerson, J. H. [1 ,2 ]
机构
[1] Vanderbilt Univ, Dept Phys & Astron, Nashville, TN 37234 USA
[2] Vanderbilt Univ, Vanderbilt Inst Nanoscale Sci & Engn, Nashville, TN 37234 USA
基金
美国国家科学基金会;
关键词
THIN-FILMS; MECHANISM; ELECTRODE; COLLOIDS; COATINGS; SURFACE;
D O I
10.1021/la205124s
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The controlled electrophoretic deposition of monolayers and ultrathin films of 4.0 nm TiO2 nanocrystals from stable, nonpolar solvent-based suspensions is reported. Stable suspensions were prepared in hexane, and the electrophoretic mobility of the nanocrystals was enhanced by a combination of a liquid liquid extraction followed by mechanical surfactant removal by high-speed centrifugation. The controlled evolution of the density of TiO2 nanocrystal monolayers was studied by transmission electron microscopy and optical transmittance spectroscopy. Ultrathin films were assembled while maintaining monolayer-by-monolayer growth and uniform density of the film. A time-dependent, equivalent circuit model has been proposed to characterize the electrophoretic current that was recorded during our experiments. Further, we demonstrate that the proposed model, coupled with the mobility, provides a means to estimate the deposition rate and, hence, the time necessary to fabricate a submonolayer, a monolayer, and multilayers of nanocrystals.
引用
收藏
页码:5295 / 5301
页数:7
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