Randomness is an inherent property of biological systems. In contrast, randomness has been mostly avoided in designing synthetic or artificial systems. Particularly, in designing micro/nano-motors, some researchers have successfully used external fields to gain deterministic control over the directionality of the objects, which otherwise move in completely random directions due to Brownian motion. However, a partial control that preserves a certain degree of randomness can be very useful in certain applications of micro/nano-motors. In this Perspective we review the current progress in establishing autonomous motion of micro/nano-particles that possess controlled randomness, provide insight into the phenomena where macroscopic order originates from microscopic disorder and discuss the resemblance between these artificial systems and biological emergent/collective behaviors.
We use the "stimulus-quench-fuse" (SQF) technique to fabricate micrometer-size colloidal heterodoublets. The doublets consist of silver and magnetic Dynabead microspheres, and the stimulus is a temporal lowering of the pH. The resulting asymmetric colloidal doublets behave as catalytic motors and show self-propulsion and phototaxis under ultraviolet (UV) light in the presence of hydrogen peroxide (H(2)O(2)), by the mechanism of diffusiophoresis. The magnetic heterodoublets show autonomous movement, in random directions, in the presence of H(2)O(2) and UV light, but if an external magnetic field is also present, they align themselves and show a directed motion forming exclusion regions around them. The assembly process described in this Article can be adapted to a wide variety of materials providing a simple, quick, inexpensive, reliable, and scalable approach for the development of synthetic motors capable of performing directed motion and forming exclusion zones and patterns.
Localization of large electric fields in plasmonic nanostructures enables various processes such as single molecule detection, higher harmonic light generation, and control of molecular fluorescence and absorption. High-throughput, simple nanofabrication techniques are essential for implementing plasmonic nanostructures with large electric fields for practical applications. In this article we demonstrate a scalable, rapid, and inexpensive fabrication method based on the salting-out quenching technique and colloidal lithography for the fabrication of two types of nanostructures with large electric field: nanodisk dimers and cusp nanostructures. Our technique relies on fabricating polystyrene doublets from single beads by controlled aggregation and later using them as soft masks to fabricate metal nanodisk dimers and nanocusp structures. Both of these structures have a well-defined geometry for the localization of large electric fields comparable to structures fabricated by conventional nanofabrication techniques. We also show that various parameters in the fabrication process can be adjusted to tune the geometry of the final structures and control their plasmonic properties. With advantages in throughput, cost, and geometric tunability, our fabrication method can be valuable in many applications that require plasmonic nanostructures with large electric fields.
This letter describes the maskless fabrication of nanowells on a silicon substrate using chemically reactive nanoparticles. The amidine-functionalized polystyrene latex (APSL) colloids are adhered onto a silicon wafer, and hydrolysis of the particles' amidine groups generates the ammonium hydroxide etchant locally. The localized release of reactive species and its fast diffusion into the bulk liquid ensure that the silicon etching takes place only under the APSL colloids. Thus, the basal length of the nanowells is precisely controlled by the diameter of the APSL particles. The shape of the nanowells depends on the structure of the substrate: inverted pyramids on silicon (100) and hexagonal pits on silicon (111). The method described here provides an easy, inexpensive, safe, and high-throughput approach for generating nanowells on silicon surfaces. This maskless and simple nanofabrication method will open doors for new applications with locally generated or locally delivered chemistry from nanoparticles.
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