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The present study suggests a novel method to produce raspberry-like microparticles containing diverse functional materials inside. The raspberry-like microparticles were produced from a random assembly of uniformly-sized poly(methyl methacrylate) (PMMA) nanoparticles via electrospraying. The solution containing the PMMA nanoparticles were supplied through the inner nozzle and compressed air was emitted through the outer nozzle. The air supply helped fast evaporation of acetone, so it enabled copious amount of microparticles as dry powder. The microparticles were highly porous both on the surface and interiors, hence various materials with a function of UV-blocking (TiO2 nanoparticles and methoxyphenyl triazine) or antiaging (ethyl(4-(2,3-dihydro-1H-indene-5-carboxyamido) benzoate)) were loaded in large amount (17 wt % versus PMMA). The surface and interior structures of the microparticles were dependent on the characteristics of functional materials. The results clearly suggest that the process to prepare the raspberry-like microparticles can be an excellent approach to generate functional microstructures. [ABSTRACT FROM AUTHOR]

Foldable polymer thin film transistors gated by an ion gel dielectric were fabricated on a polymer substrate. Side gate structure was employed to simplify the fabrication process, which is a unique advantage of the transistors based on the ion gel dielectric. Utilizing the diffusion of crosslinkable oligomers in the P3HT thin films followed by UV gelation through a patterned mask, the ion gel made a strong bonding to the P3HT layer. Due to the deformable nature of the ion gel dielectric, the transistor arrays were electrically and mechanically stable at repeated folding events. [ABSTRACT FROM AUTHOR]

A spontaneous assembly route to form a thin film of nanowires (NWs) was demonstrated and its feasibility was confirmed through the fabrication of a high-performance multi-Si NW field effect transistor (FET) using this route. Governed by the three mechanisms of spreading, trapping, and two-dimensional packing, the route was optimized for the concentration of Si NWs and the initial volume ratio of aqueous hydrochloride solution to isopropyl alcohol. The successfully formed Si NW thin-film was transferred on a flat polydimethylsiloxane (PDMS) mold and regulated using a repeatable conformal contact method with a new flat PDMS to prepare it for decal printing on an organic dielectric layer. Finally, after depositing the source and drain electrodes on the printed active layer, a high-performance 23-bridged Si NW FET exhibiting a μeffof 51.4 cm2V−1s−1, an on/off drain current ratio of 105, and a Vthof −2.7 V was obtained. [ABSTRACT FROM AUTHOR]

Uniform regio-regular poly(3-hexylthiophene) nanofibers and their blend nanofibers with poly(-caprolactone) have been obtained by electrospinning and their electrical properties in single nanofiber field effect transistors have been compared. The key to the success was restricting the precipitation of P3HT at the nozzle tip, therefore preventing the nozzle from being clogged. The field effect mobility of pure P3HT fibers was 0.017 cm2V−1s−1which is acceptable for device fabrication. Blend fibers with PCL also showed field effect behaviour with slightly degraded electrical properties by an order or two. [ABSTRACT FROM AUTHOR]

Spherical polymeric core−shell microcapsules in uniform size were produced by electrospraying with a coaxial nozzle setup. Contrary to the usual coaxial setup, the inner nozzle was slightly bent to touch the inside wall of the outer nozzle. A polymer solution for the core was introduced through the outer nozzle, and the other solution for the shell was supplied through the inner nozzle. The setup greatly increased reproduction of the same results. As a proof of the concept, core−shell microcapsules consisting of a PS or PMMA core and a PCL shell (PSPCL, PMMAPCL) were produced. When the volumetric feed rate of the shell-forming PCL solution was higher than that of the core-forming PS or PMMA solution the core−shell structures in uniform size were readily obtained. In contrast, irregular morphologies were observed when the feed rate of the PCL solution was slower or equal to that of the PS or PMMA solution. The size of the colloid was dependent on the relative feed ratio between the polymer solutions as well as the magnitude of applied voltage. [ABSTRACT FROM AUTHOR]

Colloidal particles with hollow interiors play important roles in microencapsulation—a process that has found widespread use in applications such as controlled release of drugs, cosmetics, inks, pigments or chemical reagents; protection of biologically active species; and removal of pollutants. The hollow particles are most commonly prepared by coating the surfaces of colloidal templates with thin layers of the desired material (or its precursor), followed by selective removal of the templates by means of calcination or chemical etching. This simple and straightforward approach works for a variety of materials that include polymers, ceramics, composites and metals. For polymers, methods such as emulsion polymerization, phase separation, crosslinking of micelles and self-assembly have also been demonstrated for generating hollow structures. However, diffusion through these closed shells with pores <10 nm is often a slow process. To solve this problem, macroporous capsules have been fabricated by organizing colloids around liquid droplets to form colloidosomes or by controlling the mixing of liquid droplets. Here we report the preparation of another class of macroporous capsules—polymer shells with controllable holes in their surfaces. After loading of functional materials, the holes can be closed by means of thermal annealing or solvent treatment. [ABSTRACT FROM AUTHOR]

In the last decade, extensive studies have been conducted to realize the functions of human skin based on stretchable electronics. An artificial skin, recognizing complex mechanical stimulation including pressure, strain and shear, and composed of transparent material, is an essential goal but has hardly been achieved. We fabricated a transparent integrated sensor system that can sense the strain direction and normal pressure of applied mechanical stimulation. Each sensor is composed of micropatterned Ag nanowire, forming a composite stretchable conductor with a block copolymer elastomer. The micropatterning and transfer process using thermoplastic elastomer facilitates the transparent conductor to show high transmittance with low sheet resistance at the same time. The designed transparent strain sensor responds linearly to strain, but does not respond to the orthogonal direction, which enables it to have strain-directionality. The applied mechanical signal, comprising normal force and directional strain, can be interpreted through the electrical signal observed from integrated sensors. [ABSTRACT FROM AUTHOR]

We present patterned Ag-nanowire (AgNW) networks for their application to transparent electrodes in flexible devices. Using capillary-force-based soft lithography (CFL), we formed 25- to 30-µm-wide line patterns of AgNWs on flexible polymer substrates. Organic light-emitting diodes (OLEDs) and transparent thin-film heaters (TFHs) were successfully fabricated on the patterned substrates, which verified the potential of AgNW patterns formed by CFL as interconnects in flexible devices. [ABSTRACT FROM AUTHOR]

This study investigated the surface energy-controlled transformation of amorphous Se (a-Se) colloids into trigonal Se (t-Se) crystals on solid substrates. Hydrophilic surfaces generated nanowires laterally grown along the surface of the substrates, while on hydrophobic surfaces the nanowires on the colloidal surface were randomly oriented. The ripening was considered to govern the growth of t-Se nanowires. The in-plane growth of the nanowires along the substrates made possible the creation of a chemically interconnected nanowire network because the nanowires made branches on meeting other a-Se colloids and formed chemical junctions on encountering other growing nanowires. [ABSTRACT FROM AUTHOR]

Generating laterally ordered, ultradense, macroscopic arrays of nanoscopic elements will revolutionize the microelectronic and storage industries. We used faceted surfaces of commercially available sapphire wafers to guide the self-assembly of block copolymer microdomains into oriented arrays with quasi-long-range crystalline order over arbitrarily large water surfaces. Ordered arrays of cylindrical microdomains 3 nanometers in diameter, with areal densities in excess of 10 terabits per square inch, were produced. The sawtoothed substrate topography provides directional guidance to the self-assembly of the block copolymer, which is tolerant of surface defects, such as dislocations. The lateral ordering and lattice orientation of the single-grain arrays of microdomains are maintained over the entire surface. The approach described is parallel, applicable to different substrates and block copolymers, and opens a versatile route toward ultrahigh-density systems. [ABSTRACT FROM AUTHOR]