Publications by authors named "Alvin T L Tan"

Reconfigurable metamaterials require constituent nanostructures to demonstrate switching of shapes with external stimuli. Yet, a longstanding challenge is in overcoming stiction caused by van der Waals forces in the deformed configuration, which impedes shape recovery. Here, we introduce stiff shape memory polymers.

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Evaporative self-assembly of semiconducting polymers is a low-cost route to fabricating micrometer and nanoscale features for use in organic and flexible electronic devices. However, in most cases, rate is limited by the kinetics of solvent evaporation, and it is challenging to achieve uniformity over length- and time-scales that are compelling for manufacturing scale-up. In this study, we report high-throughput, continuous printing of poly(3-hexylthiophene) (P3HT) by a modified doctor blading technique with oscillatory meniscus motion-meniscus-oscillated self-assembly (MOSA), which forms P3HT features ∼100 times faster than previously reported techniques.

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Materials made by directed self-assembly of colloids can exhibit a rich spectrum of optical phenomena, including photonic bandgaps, coherent scattering, collective plasmonic resonance, and wave guiding. The assembly of colloidal particles with spatial selectivity is critical for studying these phenomena and for practical device fabrication. While there are well-established techniques for patterning colloidal crystals, these often require multiple steps including the fabrication of a physical template for masking, etching, stamping, or directing dewetting.

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Colloidal assembly is an attractive means to control material properties via hierarchy of particle composition, size, ordering, and macroscopic form. However, despite well-established methods for assembling colloidal crystals as films and patterns on substrates, and within microscale confinements such as droplets or microwells, it has not been possible to build freeform colloidal crystal structures. Direct-write colloidal assembly, a process combining the bottom-up principle of colloidal self-assembly with the versatility of direct-write 3D printing, is introduced in the present study.

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Fluorescence quenching microscopy (FQM) is demonstrated as a low-cost and high-throughput technique for seeing graphene-like 2D sheets such as MoS2 . FQM provides high contrast and layer resolution comparable to those of scanning electron microscopy, but allows the imaging of samples deposited on arbitrary substrates, including non-conductive substrates such as quartz. Solution fluorescence quenching studies suggest that FQM should be feasible for many other 2D materials such as WS2 , Bi2 Te3 , MoSe2 , NbSe2 , and TaS2 .

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Oxidative etching of graphene flakes was observed to initiate from edges and the occasional defect sites in the basal plane, leading to reduced lateral size and a small number of etch pits. In contrast, etching of highly defective graphene oxide and its reduced form resulted in rapid homogeneous fracturing of the sheets into smaller pieces. On the basis of these observations, a slow and more controllable etching route was designed to produce nanoporous reduced graphene oxide sheets by hydrothermal steaming at 200 °C.

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Graphene oxide (GO) nanocolloids-sheets with lateral dimension smaller than 100 nm-were synthesized by chemical exfoliation of graphite nanofibers, in which the graphene planes are coin-stacked along the length of the nanofibers. Since the upper size limit is predetermined by the diameter of the nanofiber precursor, the size distribution of the GO nanosheets is much more uniform than that of common GO synthesized from graphite powders. The size can be further tuned by the oxidation time.

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