Mohamed Asbahi

Directed Self-Assembly of Densely Packed Gold Nanoparticles

Directing the self-assembly of sub-10-nm nanoparticles has been challenging because of the simultaneous requirements to achieve a densely packed monolayer and rearrange nanoparticles to assemble within a template. We met both requirements by separating the processes into two steps by first forming a monolayer of gold nanoparticles on a suitable liquid subphase of anisole and then transferring it edgewise onto a silicon substrate with a prepatterned template comprising nanoposts and nanogratings. Doing so resulted in nanoparticles that assembled in commensuration with the template design while exhibiting appreciable template-induced strain. These dense arrays of nanostructures could either be directly applied or used as lithographic masks in applications for light collection, chemical sensing, and data storage.

Template-Induced Structure Transition in Sub-10 nm Self-Assembling Nanoparticles

We report on the directed self-assembly of sub-10 nm gold nanoparticles confined within a template comprising channels of gradually varying widths. When the colloidal lattice parameter is mismatched with the channel width, the nanoparticles rearrange and break their natural close-packed ordering, transiting through a range of structural configurations according to the constraints imposed by the channel. While much work has been done in assembling ordered configurations, studies of the transition regime between ordered states have been limited to microparticles under applied compression. Here, with coordinated experiments and Monte Carlo simulations we show that particles transit through a more diverse set of self-assembled configurations than observed for compressed systems. The new insight from this work could lead to the control and design of complex self-assembled patterns other than periodic arrays of ordered particles.

Large Area Directed Self-Assembly of Sub-10 nm Particles with Single Particle Positioning Resolution

Directed self-assembly of nanoparticles (DSA-n) holds great potential for device miniaturization in providing patterning resolution and throughput that exceed existing lithographic capabilities. Although nanoparticles excel at assembling into regular close-packed arrays, actual devices on the other hand are often laid out in sparse and complex configurations. Hence, the deterministic positioning of single or few particles at specific positions with low defect density is imperative. Here, we report an approach of DSA-n that satisfies these requirements with less than 1% defect density over micrometer-scale areas and at technologically relevant sub-10 nm dimensions. This technique involves a simple and robust process where a solvent film containing sub-10 nm gold nanoparticles climbs against gravity to coat a prepatterned template. Particles are placed individually into nanoscale cavities, or between nanoposts arranged in varying degrees of geometric complexity. Brownian dynamics simulations suggest a mechanism in which the particles are pushed into the template by a nanomeniscus at the drying front. This process enables particle-based self-assembly to access the sub-10 nm dimension, and for device fabrication to benefit from the wealth of chemically synthesized nanoparticles with unique material properties.

Nanostructure Formation by controlled dewetting on patterned substrates: A combined theoretical, modeling and experimental study

We perform systematic two-dimensional energetic analysis to study the stability of various nanostructures formed by dewetting solid films deposited on patterned substrates. Our analytical results show that by controlling system parameters such as the substrate surface pattern, film thickness and wetting angle, a variety of equilibrium nanostructures can be obtained. Phase diagrams are presented to show the complex relations between these system parameters and various nanostructure morphologies. We further carry out both phase field simulations and dewetting experiments to validate the analytically derived phase diagrams. Good agreements between the results from our energetic analyses and those from our phase field simulations and experiments verify our analysis. Hence, the phase diagrams presented here provide guidelines for using solid-state dewetting as a tool to achieve various nanostructures.

High aspect ratio 10-nm-scale nanoaperture arrays with template-guided metal dewetting

We introduce an approach to fabricate ordered arrays of 10-nm-scale silica-filled apertures in a metal film without etching or liftoff. Using low temperature (<400°C) thermal dewetting of metal films guided by nano-patterned templates, apertures with aspect ratios up to 5:1 are demonstrated. Apertures form spontaneously during the thermal process without need for further processing. Although the phenomenon of dewetting has been well studied, this is the first demonstration of its use in the fabrication of nanoapertures in a spatially controllable manner. In particular, the achievement of 10-nm length-scale patterning at high aspect ratio with thermal dewetting is unprecedented. By varying the nanotemplate design, we show its strong influence over the positions and sizes of the nanoapertures. In addition, we construct a three-dimensional phase field model of metal dewetting on nano-patterned substrates. The simulation data obtained closely corroborates our experimental results and reveals new insights to template dewetting at the nanoscale. Taken together, this fabrication method and simulation model form a complete toolbox for 10-nm-scale patterning using template-guided dewetting that could be extended to a wide range of material systems and geometries.

Directed Self-Assembly of sub-10 nm Particles: Role of Driving Forces and Template Geometry in Packing and Ordering

By comparing the magnitude of forces, a directed self-assembly mechanism has been suggested previously in which immersion capillary is the only driving force responsible for packing and ordering of nanoparticles, which occur only after the meniscus recedes. However, this mechanism is insufficient to explain vacancies formed by directed self-assembly at low particle concentrations. Utilizing experiments, and Monte Carlo and Brownian dynamics simulations, we developed a theoretical model based on a new proposed mechanism. In our proposed mechanism, the competing driving forces controlling the packing and ordering of sub-10 nm particles are (1) the repulsive component of the pair potential and (2) the attractive capillary forces, both of which apply at the contact line. The repulsive force arises from the high particle concentration, and the attractive force is caused by the surface tension at the contact line. Our theoretical model also indicates that the major part of packing and ordering of nanoparticles occurs before the meniscus recedes. Furthermore, utilizing our model, we are able to predict the various self-assembly configurations of particles as their size increases. These results lay out the interplay between driving forces during directed self-assembly, motivating a better template design now that we know the importance and the dominating driving forces in each regime of particle size.

Recording performances in perpendicular magnetic patterned media

We report on the recording performances and signal-to-noise ratio (SNR) analyses of perpendicular magnetic bit-patterned media. Two different types of magnetic samples are investigated. They differ by the way that they were patterned (nano-imprint versus e-beam lithography) as well as their magnetic properties (Co/Pt multilayers and CoCrPt alloy are the recording layers).Using a contact read/write quasi-static tester, we were able to characterize the write windows, the bit error rates and measure the SNR. The influence of magnetic properties and media microstructure on the writing processes is studied. We show also that the lithographical method used to replicate the media induces more or less noise due to structural distributions.

A facile approach for screening isolated nanomagnetic behavior for bit-patterned media

Bit-patterned media (BPM) fabricated by the direct deposition of magnetic material onto prepatterned arrays of nanopillars is a promising approach for increasing magnetic recording of areal density. One of the key challenges of this approach is to identify and control the magnetic interaction between the bits (on top of the nanopillars) and the trench material between the pillars. Using independent techniques, including magnetic force microscopy, the variable-angle magneto-optic Kerr effect, and remanence curves, we were able to determine the presence and relative intensities of exchange and dipolar interactions in Co-Pd multilayer-based BPM fabricated by direct deposition. We found that for pitches of 30 nm or less, there were negligible exchange interactions, and the bits were found to be magnetically isolated. As we move to higher densities, the absence of exchange interactions indicates that direct deposition is a promising approach to BPM fabrication.

Determination of Position Jitter and Dot-Size Fluctuations in Patterned Arrays Fabricated by the Directed Self-Assembly of Gold Nanoparticles

The promise of magnetic bit-patterned media (BPM) in the hard disk drive industry hinges on its capability to extend the data storage density beyond that achievable by conventional continuous media. Its success, however, depends strongly on meeting the jitter and throughput requirements of BPM with a suitable fabrication process. In this paper, we report on the directed self-assembly of gold nanoparticles using a topographical template as an approach to fulfill the BPM fabrication requirements. The effects of position jitter and dot-size fluctuations are examined by performing image analysis on scanning electron microscopies of samples fabricated with areal densities of 4.4 Tdot/in2. For comparison, we considered three different cases: electron-beam lithography-defined templates, monolayer films of self-assembled nanoparticles on an unpatterned substrate, and nanoparticles directed to assemble within a template. Our analysis provides evidence for the improvements in position jitter of the directed assembly of nanoparticles over those that were left to assemble without a template.

Directed self-assembly of sub-10 nm particle clusters using topographical templates

Directed self-assembly of nanoparticles (DSA-n) is an approach that creates suitable conditions to capture nanoparticles randomly dispersed in a liquid and position them into predefined locations on a solid template. Although DSA-n is emerging as a potential bottom-up patterning technique to build nanostructures using nanoparticles of various sizes, geometries and material compositions, there are still several outstanding challenges. In this paper, we focus on the DSA-n of sub-10 nm particles using topographical templates to guide them into 1D and 2D ordered arrays. The process mechanism leading DSA-n at sub-10 nm size scale has been reviewed and experimental evidence of the impact of the template on the positioning both individual and clusters of particles with low level of structure defects have also been demonstrated. Furthermore, by controlling the drying direction of the liquid within polygonal traps, we are also able to tune the spacing between the trapped nanoparticle clusters. This self-structuring phenomenon is of crucial importance for various applications such as plasmonics and charge transport within quantum circuits, whereby the coupling effects are highly dependent on the size of the nanoparticles and their separation.