Directed assembly of nanodiamond nitrogen-vacancy centers on a chemically modified patterned surface.

Nitrogen-vacancy (NV) centers in nanodiamond (ND) particles are an attractive material for photonic, quantum information, and biological sensing technologies due to their optical properties-bright single photon emission and long spin coherence time. To harness these features in practical devices, it is essential to realize efficient methods to assemble and pattern NDs at the micro-/nanoscale. In this work, we report the large scale patterned assembly of NDs on a Au surface by creating hydrophobic and hydrophilic regions using self-assembled monolayer (SAM). Hydrophobic regions are created using a methyl (-CH3) terminated SAM of octadecanethiol molecules. Evaporating a water droplet suspension of NDs on the SAM patterned surface assembles the NDs in the bare Au, hydrophilic regions. Using this procedure, we successfully produced a ND structures in the shape of dots, lines, and rectangles. Subsequent photoluminescence imaging of the patterned NDs confirmed the presence of optically active NV centers. Experimental evidence in conjunction with computational analysis indicates that the surface wettability of the SAM modified Au surface plays a dominant role in the assembly of NDs as compared to van der Waals and other substrate-ND interactions.

"Sliding kinetics" of single-walled carbon nanotubes on self-assembled monolayer patterns: beyond random adsorption.

We present the experimental results and theoretical model describing new adsorption kinetics of single-walled carbon nanotubes (swCNTs) onto self-assembled monolayer (SAM) including their sliding motion. The adsorption behavior of swCNTs on large-size SAM patterns is similar to the Langmuir isotherm, while that on nanoscale patterns shows a significant deviation which can be explained by the sliding motion of adsorbed nanotubes. The "sliding chamber" experiment confirms that swCNTs can align along the SAM patterns by sliding motion right above the SAM surfaces. This result provides new scientific insights regarding the adsorption kinetics of one-dimensional nanostructures, and, from a practical point of view, it can be an important guideline to design SAM patterns to assemble carbon nanotubes and nanowires into desired device structures.

"Lens" effect in directed assembly of nanowires on gradient molecular patterns.

We report a new phenomenon, named here as the "lens" effect, in the directed-assembly process of nanowires (NWs) on self-assembled monolayer (SAM) patterns. In this process, the adsorption of NWs is focused in the nanoscale regions at the center of microscale SAM patterns with gradient surface molecular density just like an optical lens focuses light. As a proof of concepts, we successfully demonstrated the massive assembly of V2O5 NWs and single-walled carbon nanotubes (swCNTs) with a nanoscale resolution using only microscale molecular patterning methods. This work provides us with important insights about the directed-assembly process, and from a practical point of view, it allows us to generate nanoscale patterns of NWs over a large area for mass fabrication of NW-based devices.

Directed-assembly of single-walled carbon nanotubes using self-assembled monolayer patterns comprising conjugated molecular wires.

Self-assembled monolayer (SAM) patterns on electrodes are often utilized to guide the assembly of single-walled carbon nanotubes (SWCNTs) onto the electrodes to form desired device structures. In this case, the SWCNTs are in contact with the electrodes through the SAM which comprises molecular wires. Presumably, it is desirable to use conjugated molecular wires for a low contact resistance because they have been reported as a better electric conductor than non-conjugated ones. However, until now, the directed-assembly of SWCNTs has been driven mostly via molecular wires with alkane backbones which are known to be relatively poor conductors. Herein, we report large-scale directed-assembly of SWCNTs utilizing SAM patterns comprising conjugated molecular wires. We achieved highly selective adsorption and precision alignment of SWCNTs utilizing polar SAM patterns comprising conjugated molecular wires, while SAM patterns with non-polar terminal groups efficiently prevented adsorption of SWCNTs. Furthermore, we developed a process for assembling a SWCNT across two electrodes coated with conjugated molecular wires, and the electrical conduction through the SWCNT was measured via a conducting atomic force microscope. This result could be an important guideline for large-scale directed-assembly of SWCNT-based devices in the future.

Nanotube electronics: large-scale assembly of carbon nanotubes.

Nanoscale electronic devices made from carbon nanotubes, such as transistors and sensors, are much smaller and more versatile than those that rely on conventional microelectronic chips, but their development for mass production has been thwarted by difficulties in aligning and integrating the millions of nanotubes required. Inspired by biomolecular self-assembly processes, we have created chemically functionalized patterns on a surface, to which pre-grown nanotubes in solution can align themselves in huge numbers. This method allows wafer-scale fabrication of millions of carbon-nanotube circuits with single-nanotube precision, and may enable nanotube-based devices, such as computer chips and high-density sensor arrays, to be produced industrially.