Engineering the Spatial Selectivity of Surfaces at the Nanoscale Using Particle Lithography Combined with Vapor Deposition of Organosilanes

被引:60
作者
Li, Jie-Ren [1 ,2 ]
Lusker, Kathie L. [1 ,2 ]
Yu, Jing-Jiang [3 ]
Garno, Jayne C. [1 ,2 ]
机构
[1] Louisiana State Univ, Dept Chem, Baton Rouge, LA 70803 USA
[2] Louisiana State Univ, Ctr BioModular Multiscale Syst, Baton Rouge, LA 70803 USA
[3] Agilent Technol, Nanotechnol Measurements Div, Chandler, AZ 85226 USA
基金
美国国家科学基金会;
关键词
particle lithography; atomic force microscopy; nanopatterns; organosilanes; self-assembled monolayers; gold nanoparticles; nanolithography; SELF-ASSEMBLED MONOLAYER; DIP-PEN NANOLITHOGRAPHY; ATOMIC-FORCE MICROSCOPY; LARGE-SCALE FABRICATION; CONSTRUCTIVE NANOLITHOGRAPHY; GOLD NANOPARTICLES; PROTEIN NANOSTRUCTURES; MACROPOROUS POLYMERS; COLLOID MONOLAYERS; SILICON;
D O I
10.1021/nn9004796
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Particle lithography is a practical approach to generate millions of organosilane nanostructures on various surfaces, without the need for vacuum environments or expensive instrumentation. This report describes a stepwise chemistry route to prepare organosilane nanostructures and then apply the patterns as a spatially selective foundation to attach gold nanoparticles. Sites with thiol terminal groups were sufficiently small to localize the attachment of clusters of 2-5 nanoparticles. Basic steps such as centrifuging, drying, heating, and rinsing were used to generate arrays of regular nanopatterns. Close-packed films of monodisperse latex spheres can be used as an evaporative mask to spatially direct the placement of nanoscopic amounts of water on surfaces. Vapor phase organosilanes deposit selectively at areas of the surface containing water residues to generate nanostructures with regular thickness, geometry, and periodicity as revealed in atomic force microscopy images, The area of contact underneath the mesospheres is effectively masked for later synthetic steps, providing exquisite control of surface coverage and local chemistry. By judicious selection in designing the terminal groups of organosilanes, surface sites can be engineered at the nanoscale for building more complex structures. The density of the nanopatterns and surface coverage scale predictably with the diameter of the mesoparticle masks. The examples presented definitively illustrate the capabilities of using the chemistry of molecularly thin films of organosilanes to spatially define the selectivity of surfaces at very small size scales.
引用
收藏
页码:2023 / 2035
页数:13
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