Self-assembly of monodisperse colloidal particles into regular lattices has provided relatively simple and economical methods to prepare photonic crystals. The photonic stop band of colloidal crystals appears as opalescent structural colors, which are potentially useful for display devices, colorimetric sensors, and optical filters. However, colloidal crystals have low durability, and an undesired scattering of light makes the structures white and translucent. Moreover, micropatterning of colloidal crystals usually requires complex molding procedures, thereby limiting their practical applications. To overcome such shortcomings, we develop a pragmatic and amenable method to prepare colloidal photonic crystals with high optical transparency and physical rigidity using photocurable colloidal suspensions. The colloidal particles dispersed in a photocurable medium crystallized during capillary force-induced infiltration into a slab, and subsequent photopolymerization of the medium permanently solidifies the structures. Furthermore, conventional photolithography enables micropatterning of the crystal structures. The low index contrast between particles and matrix results in high transparency of the resultant composite structures and narrow reflection peaks, thereby enabling structural color mixing through the overlapping of distinct layers of the colloidal crystals. Multiple narrow peaks in the spectrum provide high selectivity in optical identification, thereby being potentially useful for security materials.

Microencapsulation and controlled release have long been studied because of the high demand for practical delivery systems in the pharmaceutics and cosmetics fields. Multiphase emulsion drops have provided efficient templates for microcapsules, and various feasible methods have been developed for controlled release.[1] However, the emulsion-based approach has limitations for the in situ control of membrane permeability. Micro-origami has emerged as one of the most promising alternative approaches for producing tunable microcapsules with the potential to be applied, for example as drug carriers, [2] actuators, [3] microcontainers, [4] and microrobots.[5] Inspired by living organisms in nature such as the ice plant [6] and Venus flytrap, [7] two different micro-origami approaches have been employed to make various microstructures.[8] One approach uses solid patches connected by active hinge materials. Typical examples use various metalmetal, [9] metal-polymer, [10] and polymer-polymer [4] combinations. The patch and hinge system has enabled the capture, release, and gripping [11] of target materials, showing the feasibility of micro-origami structures. However, the microcapsule is limited to polyhedral shapes in this approach, and complete sealing of the gaps between patches requires exquisite control of the folding angles. Moreover, the delicate and complex fabrication processes make practical applications difficult. The second approach uses a bilayer structure composed of two different materials. For example, a metalpolymer bilayer can show bending/unbending when the polymeric active layer suffers significant volume change, but the metal layer remains unchanged. [12,13] Polymer materials have been employed in both layers to make biocompatible microcapsules. [14,15] However, complete sealing of the gaps in the bilayer contact regions remains an important, yet unmet, need. In addition, a simple and effective method for the fabrication of practical microcapsules has not yet been developed, and remains highly desirable. This is the main thrust of the present study.Herein, we report the use of biocompatible bilayer structures for the fabrication of tunable microcapsules based on micro-origami. Monodisperse bilayer microstructures were prepared using a facile photolithographic procedure, without employing photomask alignment. In addition, highly flexible hydrogels were selected as both active and passive layers, facilitating tight contact between patches. The bilayer structure therefore enabled in situ encapsulation, through a reversible transformation to microcapsules with a closed compartment. The resultant microcapsules showed negligible leakage of encapsulants and triggered release of the encapsulants could be achieved simply by inducing the unfolding of the hydrogel bilayer.The essential strategy of our approach relies on the anisotropic volume change of a hydrogel bilayer. As shown in Scheme 1 a, the active hydrogel layer shows significant volume expansion under external stimuli by swelling, whereas the passive h...

Isotropic microparticles prepared from a suspension that undergoes polymerization have long been used for a variety of applications. Bulk emulsification procedures produce polydisperse emulsion droplets that are transformed into spherical microparticles through chemical or physical consolidation. Recent advances in droplet microfluidics have enabled the production of monodisperse emulsions that yield highly uniform microparticles, albeit only on a drop-by-drop basis. In addition, microfluidic devices have provided a variety of means for particle functionalization through shaping, compartmentalizing, and microstructuring. These functionalized particles have significant potential for practical applications as a new class of colloidal materials. This feature article describes the current state of the art in the microfluidic-based synthesis of monodisperse functional microparticles. The three main sections of this feature article discuss the formation of isotropic microparticles, engineered microparticles, and hybrid microparticles. The complexities of the shape, compartment, and microstructure of these microparticles increase systematically from the isotropic to the hybrid types. Each section discusses the key idea underlying the design of the particles, their functionalities, and their applications. Finally, we outline the current limitations and future perspectives on microfluidic techniques used to produce microparticles.

Dynamic modulation of photonic bandgaps in crystalline colloidal arrays is achieved by application of electric field. Highly charged polystyrene particles spontaneously create the crystal lattice, which is compressed or relaxed under external electric field by electrokinetic force. As a result, structural color of colloidal crystals as a photonic bandgap can be tuned or fixed with unprecedentedly fast and precise manner.

Recent advances in microfluidics have enabled the controlled production of multiple-emulsion drops with onion-like topology. The multiple-emulsion drops possess an intrinsic core-shell geometry, which makes them useful as templates to create microcapsules with a solid membrane. High flexibility in the selection of materials and hierarchical order, achieved by microfluidic technologies, has provided versatility in the membrane properties and microcapsule functions. The microcapsules are now designed not just for storage and release of encapsulants but for sensing microenvironments, developing structural colours, and many other uses. This article reviews the current state of the art in the microfluidic-based production of multiple-emulsion drops and functional microcapsules. The three main sections of this paper discuss distinct microfluidic techniques developed for the generation of multiple emulsions, four representative methods used for solid membrane formation, and various applications of functional microcapsules. Finally, we outline the current limitations and future perspectives of microfluidics and microcapsules.

Active materials that respond to physical and chemical stimuli can be used to build dynamic micromachines that lie at the interface between biological systems and engineered devices. In principle, the specific hybridization of DNA can be used to form a library of independent, chemically driven actuators for use in such microrobotic applications and could lead to device capabilities that are not possible with polymer- or metal-layer-based approaches. Here, we report shape changing films that are powered by DNA strand exchange reactions with two different domains that can respond to distinct chemical signals. The films are formed from DNA-grafted gold nanoparticles using a layer-by-layer deposition process. Films consisting of an active and a passive layer show rapid, reversible curling in response to stimulus DNA strands added to solution. Films consisting of two independently addressable active layers display a complex suite of repeatable transformations, involving eight mechanochemical states and incorporating self-righting behaviour.

Omniphobic surfaces are created by designing an array of overhanging microdisks on a polymer film through two steps of photolithography. Two distinct edges and the large height of the microdisks relative to their separation ensure the formation of an air mat under the microdisks, providing an omniphobic property. Moreover, the freestanding omniphobic films are transparent and flexible, potentially serving as liquid-repellent surfaces in various applications.

Three-dimensional hierarchical architectures are fabricated using a simple, cost-effective, durable colloidal phase mask containing a colloidal monolayer embedded in a flexible polydimethylsiloxane (PDMS) membrane. These structures give rise to a photonic bandgap that can be tuned over a wide spectral range from the visible to the near-infrared regions.