We developed switchable Janus particles (JPs) fabricated by coating one hemisphere of silica microspheres with a phase-change film. We used the chalcogenide GeSbTe (GST), which exhibits a reversible phase change between a metal-like crystalline phase (c-GST) and a dielectric-like amorphous phase (a-GST). As a driving force for self-propelling the JPs, a perpendicular alternating current electric field was applied; the frequency dependence of the motion of an individual JP and that of inter-JP interaction were investigated. At lower frequencies (2–20 kHz), a-GST JPs were propelled with their silica side facing forward, which is similar to the behavior of Au–silica JPs propelled by the well-known induced-charge electrophoresis mechanism, whereas c-GST JPs were immobile because they adhered to the indium tin oxide substrate. At higher frequencies (50–300 kHz), both a-GST and c-GST JPs were propelled with their GST side facing forward and a substantial difference in inter-JP interaction was observed: repulsive collision for c-GST JPs but attractive stacking for a-GST JPs.
Optical techniques have been actively studied for manipulating nano-to microsized objects. However, long-range attraction and rapid transport of particles within thin quasi-twodimensional systems are difficult because of the weak thermophoretic forces. Here, we introduce an experimental system that can rapidly generate quasi-two-dimensional colloidal crystals in deionized water, sandwiched between two hard plates. When a pulsed laser is irradiated on a chalcogenide phase-change material spattered on one side of the plates, the induced Marangoni-like flow causes a colloidal self-assembly in the order of tens of micrometers within the laser spot, with a transport velocity of a few tens of micrometers per second. This is due to the large thermal gradient induced by chalcogenide characteristics of high laser absorption and low thermal conductivity, and a strong hydrodynamic slip flow at the hydrophobic chalcogenide interface. Moreover, the colloidal crystals exhibit various lattice structures, depending on the laser intensity and chamber distance. For a certain range of the chamber distance, the colloidal crystal phases can be alternated by tuning the laser intensity in real time. Our system forms and deforms quasi-two-dimensional colloidal crystals at an on-demand location on a GeSbTe substrate.
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