Monolayers of Twisted Binaphthyls for Aromatic Crystallization at Low Nucleation Densities and High Growth Rates

Monolayers of 1,1‘-bi-2-naphthol (BN) derivatives, of which the two naphthalene rings are twisted along the carbon(1)−carbon(1‘) single bond, were studied for their conformational effect on the growth of pentacene crystals on their monolayer surface. BN monolayers with H and Br at 6,6‘-positions (H-BN and Br-BN) were prepared by immersion-coating in toluene solution of the corresponding BNSiCl2. Pentacene was thermally evaporated onto the H-BN and Br-BN monolayers, silica, octadecylsilyl (ODTS) SAM, and a micropattern of H-BN and ODTS SAM. Pentacene crystals were also grown on the SAMs of 1-naphthylsilyl(NPh), phenylsilyl(Ph), and diphenylsilyl (DPh) groups, which are aromatic and have contact angle values similar to those of the the BN monolayers. AFM images of the crystals at the early stage of growth indicated that the BN monolayers suppressed the nucleation while facilitating the growth of nuclei to larger crystals. The low nucleation density and high growth rate are accounted for by the amorphous nature of the twisted BN monolayer surface where the intermolecular interaction between neighboring adsorbates is likely to be suppressed. The results offer new insights into designing surfaces for controlling the crystallization kinetics of organic materials

Electrical Switching between Vesicles and Micelles via Redox-Responsive Self-Assembly of Amphiphilic Rod−Coils

An aqueous vesicular system that is switchable by electric potential without addition of any chemical redox agents into the solution is demonstrated using redox-responsive self-assembly of an amphiphilic rod−coil molecule consisting of a tetraaniline and a poly(ethylene glycol) block. The vesicle membrane is split by an oxidizing voltage into smaller pucklike micelles that can reassemble to form vesicles upon exposure to a reducing voltage. The switching mechanism is explained by the packing behavior of the tetraaniline units constituting the membrane core, which depends on their oxidation states

Hydrogen-Bonding-Facilitated Layer-by-Layer Growth of Ultrathin Organic Semiconducting Films

We demonstrated that the layer-by-layer growth of thin film crystals of conjugated organic molecules is facilitated by their hydrogen-bonding capabilities. We synthesized bis­(3-hydroxypropyl)-sexithiophene (bHP6T), which includes two hydroxyalkyl groups that promote interlayer and intermolecular molecular interactions during the crystal growth process. Under the optimal deposition conditions, the crystals grew in a nearly perfect layer-by-layer mode on the solid substrate surfaces, enabling the formation of uniform charge transporting films as thin as a few monolayers. A thin film transistor device prepared from a bHP6T film only 9 nm thick exhibited a charge carrier mobility well above 1 × 10^–2 cm²/(V s) and an on/off ratio exceeding 1 × 10⁴. These properties are better than the properties of other sexithiophene-based devices yet reported. The devices exhibited enhanced stability under atmospheric conditions, and they functioned properly, even after storage for more than 2 months

Real-Time Information-Variable Invisible Barcode Comprising Freely Deformable Infrared-Emitting Yarns

Barcodes are utilized for product information management in shops, offices, hospitals, passenger facilities, and factories because they enable substantial amounts of data to be processed quickly and accurately. However, a limited amount of information can be loaded on the currently used monochrome barcodes that are based on thin-film coatings. Therefore, these barcodes require constant replacement with new barcodes to update the information; furthermore, they cannot be applied to textile products. This study demonstrated the performance of wearable invisible infrared (IR)-emitting barcodes by using twisted yarns that comprised five highly elastic/conductive spandex fibers. The barcode information can be actively updated via the selective IR emission from specific yarns of the barcode by controlling the applied voltage to the IR-emitting yarns. Therefore, the IR barcode required a relatively small number of bars to express a higher volume of information compared to the existing monochrome barcodes. Because the emitted IR light from the yarns was invisible to the human eye and was only recognized by an IR camera, the information-variable IR-emitting yarn-based barcode exhibited an aesthetic design and was composed of a sustainable fabric-type material that could be easily applied to clothes, bags, and shoes. It is expected that the fabricated barcode will be widely utilized as wearable invisible barcodes, whose information will remain invisible to humans and can be updated in real time to ensure information fluidity

Self-Emitting Artificial Cilia Produced by Field Effect Spinning

In nature, many cells possess cilia that provide them with motor or sensory functions, allowing organisms to adapt to their environment. The development of artificial cilia with identical or similar sensory functions will enable high-performance and flexible sensing. Here, we investigate a method of producing artificial cilia composed of various polymer materials, such as polyethylene terephthalate, polyurethane, poly­(methyl methacrylate), polyvinylpyrrolidone, polystyrene, polyvinyl chloride, and poly (allylamine hydrochloride), using a field effect spinning (FES) method. Unlike wet- or electro-spinning, in which single or multiple strands of fibers are pulled without direction, the FES method can grow fiber arrays vertically and uniformly on a substrate in cilia-like patterns. The lengths and diameters of the vertically grown artificial cilia can be controlled by the precursor polymer concentration in the solution, applied electric current and voltage, and shape and size of the needle tip used for FES. The red, green, and blue emission characteristics of the polymer-quantum dot-based self-emitting artificial cilia prepared in polymer–inorganic nanoparticle hybrid form were determined. In addition, an artificial cilia-based humidity sensor made of the polymer–polymer composite was fabricated

Self-Emitting Artificial Cilia Produced by Field Effect Spinning

In nature, many cells possess cilia that provide them with motor or sensory functions, allowing organisms to adapt to their environment. The development of artificial cilia with identical or similar sensory functions will enable high-performance and flexible sensing. Here, we investigate a method of producing artificial cilia composed of various polymer materials, such as polyethylene terephthalate, polyurethane, poly­(methyl methacrylate), polyvinylpyrrolidone, polystyrene, polyvinyl chloride, and poly (allylamine hydrochloride), using a field effect spinning (FES) method. Unlike wet- or electro-spinning, in which single or multiple strands of fibers are pulled without direction, the FES method can grow fiber arrays vertically and uniformly on a substrate in cilia-like patterns. The lengths and diameters of the vertically grown artificial cilia can be controlled by the precursor polymer concentration in the solution, applied electric current and voltage, and shape and size of the needle tip used for FES. The red, green, and blue emission characteristics of the polymer-quantum dot-based self-emitting artificial cilia prepared in polymer–inorganic nanoparticle hybrid form were determined. In addition, an artificial cilia-based humidity sensor made of the polymer–polymer composite was fabricated