Facile and cost-effective fabrication of wearable alpha-naphtholphthalein-based halochromic sensor for wound pH monitoring.

The sensor, designed to be worn directly on the skin, is suitable for real-time monitoring of the recovery level of not only general wounds, but also difficult-to-heal wounds, such as those with chronic inflammation. Notably, healthy skin has a pH range of 4-6. When a wound occurs, the pH is known to be approximately 7.4. In this study, alpha-naphtholphthalein (Naph) was immersed in a cotton-blended textile to produce a wearable halochromic sensor that clearly changed color depending on the pH of the skin in the range 6-9, including pH 7.4, which is the skin infection state. The coating was performed without using an organic solvent by dissolving it in micelle form using cetyltrimethylammonium bromide, a surfactant, in water. Naph-based halochromic sensor shows light yellow, which is the dye's own color, at pH 6, which is a healthy skin condition, and gradually showed a clear color change to light green-green-blue as pH increased. Even after washing and drying by rubbing with regular tap water, the color change due to pH was maintained more than 10 times. Naph-based halochromic sensors use a simple solution production and coating method and are not only reusable sensors that can be washed with water but also use environmentally friendly water, making them very suitable for developing commercial products for wound pH monitoring. In addition, it can be easily applied to medical supplies, such as medical gauze, patient clothes, and compression bandages, as well as everyday wear, such as clothing, gloves, and socks. Therefore, it is expected to be widely used as a wound pH sensor, allowing real-time monitoring of the skin condition of individuals with chronic skin inflammation, including patients requiring wound recovery.

Cesium tungsten oxide-carbon nanotube-hydroxypropyl cellulose thermoresponsive display.

Among different heat-responsive polymers, hydroxypropyl cellulose (HPC) is biodegradable and is widely used in products that are harmless to the human body, such as food and pharmaceuticals. When the temperature of the hydrogel-type HPC increases, the hydrophilic bonds between the HPC molecules break, and the HPC molecules aggregate owing to the hydrophobic bonds. Therefore, light transmittance may vary because the aggregated HPC molecules scatter light. This study investigated the implementation of a display using the thermoreversible phase transition of HPC. Herein, a near-infrared (NIR) laser was irradiated only to a local area to control the surface temperature and enable the effective operation of the thermoreversible phase transition of HPC. For this, cesium tungsten oxide (CTO), which absorbs NIR light and generates heat, was mixed with the HPC hydrogel to improve the photothermal effect. Moreover, by additionally mixing carbon nanotubes (CNTs) with high thermal conductivity, the heat generated from the CTO is quickly transferred to the HPC hydrogel, and the heat of the HPC hydrogel is quickly cooled through the CNTs after stopping the NIR laser irradiation. The produced NIR-writing CTO-CNT-HPC (CCH) thermoresponsive display exhibited a fast thermoresponsive time. The CCH thermoresponsive display developed in this study can be applied in situations that require fast display response times, such as interactive advertising, property exhibitions, navigation systems for car, schedule information, event information, and public announcements.

Reversible thermochromic fibers with excellent elasticity and hydrophobicity for wearable temperature sensors.

Color-changing fibers, which can intuitively convey information to the human eye, can be used to facilely add functionality to various types of clothing. However, they are often expensive and complex, and can suffer from low durability. Therefore, in this study, we developed highly elastic and hydrophobic thermochromic fibers as wearable temperature sensors using a simple method that does not require an electric current. A thermochromic pigment was embedded inside and outside hydrophobic silica aerogel particles, following which the thermochromic aerogel was fixed to highly elastic spandex fibers using polydimethylsiloxane as a flexible binder. In particular, multi-strand spandex fibers were used instead of single strands, resulting in the thermochromic aerogels penetrating the inside of the strands upon their expansion by solvent swelling. During drying, the thermochromic aerogel adhered more tightly to the fibers by compressing the strands. The thermochromic fiber was purple at room temperature (25 °C), but exhibited a two-stage color change to blue and then white as the temperature increased to 37 °C. In addition, even after 100 cycles of tension-contraction at 200%, the thermochromic aerogel did not detach and was strongly attached to the fiber. Additionally, it was confirmed that color change due to temperature was stable even after exposure to 1 wt% NaCl (artificial sweat) and 0.1 wt% detergent solutions. The developed thermochromic fiber therefore exhibited excellent elasticity and hydrophobicity, and is expected to be widely utilized as an economical wearable temperature sensor as it does not require electrical devices.

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.

Information-Providing Flexible and Transparent Smart Window Display.

A smart window, which can easily adjust light transmittance, can provide barrier functions, such as improvement in energy efficiency, glare prevention, and privacy protection. However, a smart window that can selectively provide real-time information and display various colorful characters and images at a desired location has not been developed. In this study, a novel smart window capable of real-time information conversion is developed by advancing the light transmittance control of the existing smart windows. A transparent and flexible window display is fabricated by synthesizing poly(N-isopropylacrylamide) (pNIPAM)-N,N-methylenebisacrylamide-crosslinked hydrogels (NBcH) and near-infrared (NIR) absorption-heating films sandwiched between two plastic substrates. When the NIR laser irradiates the window display panel surface, the temperature rises rapidly, as the NIR absorption-heating film absorbs the NIR wavelength. The generated heat is transferred to pNIPAM in contact with the NIR absorption-heating film, and an image forms in real time. In addition, if the NIR laser and projector simultaneously irradiate the window display panel surface, various colorful images can be displayed. The smart window for real-time information provision proposed in this study acts like a glass curtain that can selectively make a desired location transparent or opaque by controlling the transmittance of light and acts as a display that can present various colorful characters and images in real time. Therefore, it is expected to be highly convenient for users.

Dipping-Press Coating Method for Retaining Transparency and Imparting Hydrophobicity Regardless of Plastic Substrate Type.

Plastics are used in cover substrates for billboards, windows, large LED signboards, lighting devices, and solar panels because they are transparent and can be colored and shaped as desired. However, when plastic cover substrates installed in outdoor environments are constantly exposed to harsh conditions such as snow, rain, dust, and wind, their transparency deteriorates owing to watermarks and dust contamination. Herein, we investigated a simple dipping-press coating method that can impart hydrophobicity while maintaining the transparency, regardless of the plastic substrate type. A highly transparent and hydrophobic coating film was formed on a plastic substrate by a two-step process, as follows: (1) application of a polydimethylsiloxane-octadecylamine coating by a dipping process, and (2) embedding (1H,1H,2H,2H-heptadecafluorodec-1-yl) phosphonic acid-aluminum oxide nanoparticles by a thermal press process. The plastic substrates on which the highly transparent and hydrophobic coating film was formed showed 150° or higher hydrophobicity and 80% or higher visible light transparency. The coating method proposed herein can easily impart hydrophobicity and is compatible with any plastic substrate that must maintain prolonged transparency without contamination when exposed to adverse conditions.

Enhancing Functionality of Epoxy-TiO2-Embedded High-Strength Lightweight Aggregates.

With the increasing trend of high-rise, large-scale, and functional modern architectural structures, lightweight aggregate (LWA) concrete that exhibits excellent strength and high functionality has garnered active research attention. In particular, as the properties of concrete vary considerably with the raw materials and the proportions of aggregates in the mix, in-depth research on weight reduction, strength improvement, and functional enhancements of aggregates is crucial. This study used the negative pressure coating of a mixed solution comprising epoxy (mixture of epoxy resin and crosslinker), hyper-crosslinked polymer, and titanium oxide (TiO2) nanoparticles on the LWA, and achieved an improvement in the strength of the LWA as well as a reduction in air pollutants such as NOx and SOx. Compared to a normal LWA with an aggregate impact value (AIV) of 38.7%, the AIV of the proposed epoxy-TiO2-embedded high-strength functional LWA was reduced by approximately half to 21.1%. In addition, the reduction rates of NOx and SOx gases resulting from the photocatalytic properties of TiO2 nanoparticles coated with epoxy were approximately 90.9% and 92.8%, respectively. Epoxy-TiO2, embedded in LWAs through a mixture, exhibited stability, high strength, and a reduction in air pollutant characteristics, despite repeated water washing. The LWA proposed herein offers excellent structural and functional properties and is expected to be used in functional lightweight concrete that can be practically applied in high-rise and large-scale architectural structures.

Superhydrophobic, Elastic, and Conducting Polyurethane-Carbon Nanotube-Silane-Aerogel Composite Microfiber.

Flexible fibers composed of a conductive material mixed with a polymer matrix are useful in wearable electronic devices. However, the presence of the conductive material often reduces the flexibility of the fiber, while the conductivity may be affected by environmental factors such as water and moisture. To address these issues, we developed a new conductive fiber by mixing carbon nanotubes (CNT) with a polyurethane (PU) matrix. A silane ((heptadecafluoro-1,1,2,2-tetra-hydrodecyl)trichlorosilane) was added to improve the strain value of the fiber from 155% to 228%. Moreover, silica aerogel particles were embedded on the fiber surface to increase the water contact angle (WCA) and minimize the effect of water on the conductivity of the fiber. As a result, the fabricated PU-CNT-silane-aerogel composite microfiber maintained a WCA of ~140° even after heating at 250 °C for 30 min. We expect this method of incorporating silane and aerogel to help the development of conductive fibers with high flexibility that are capable of stable operation in wet or humid environments.

Human sweat monitoring using polymer-based fiber.

Lightweight nano/microscale wearable devices that are directly attached to or worn on the human body require enhanced flexibility so that they can facilitate body movement and overall improved wearability. In the present study, a flexible poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) fiber-based sensor is proposed, which can accurately measure the amount of salt (i.e., sodium chloride) ions in sweat released from the human body or in specific solutions. This can be performed using one single strand of hair-like conducting polymer fiber. The fabrication process involves the introduction of an aqueous PEDOT:PSS solution into a sulfuric acid coagulation bath. This is a repeatable and inexpensive process for producing monolithic fibers, with a simple geometry and tunable electrical characteristics, easily woven into clothing fabrics or wristbands. The conductivity of the PEDOT:PSS fiber increases in pure water, whereas it decreases in sweat. In particular, the conductivity of a PEDOT:PSS fiber changes linearly according to the concentration of sodium chloride in liquid. The results of our study suggest the possibility of PEDOT:PSS fiber-based wearable sensors serving as the foundation of future research and development in skin-attachable next-generation healthcare devices, which can reproducibly determine the physiological condition of a human subject by measuring the sodium chloride concentration in sweat.

Pen drawing display.

As advancements in science and technology, such as the Internet of things, smart home systems, and automobile displays, become increasingly embedded in daily life, there is a growing demand for displays with customized sizes and shapes. This study proposes a pen drawing display technology that can realize a boardless display in any form based on the user's preferences, without the usual restrictions of conventional frame manufacturing techniques. An advantage of the pen drawing method is that the entire complex fabrication process for the display is encapsulated in a pen. The display components, light-emitting layers, and electrodes are formed using felt-tip drawing pens that contain the required solutions and light-emitting materials. The morphology and thickness of each layer is manipulated by adjusting the drawing speed, number of drawing cycles, and substrate temperature. This study is expected to usher in the upcoming era of customized displays that can reflect individual user needs.

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.

Infrared Invisibility Cloak Based on Polyurethane-Tin Oxide Composite Microtubes.

An invisibility cloak based on visible rays with a refractive index similar to that of air can effectively conceal people or objects from human eyes. However, even if an invisibility cloak based on visible rays is used, an infrared (IR) thermography camera can detect the heat (thermal radiation) emitted from different types of objects including living things. Therefore, both visible and IR rays should be shielded using an invisibility cloak produced by an appropriate technology. Herein, we developed a textile cloak that can almost completely conceal people or objects from IR vision. If a person or object is covered with an IR- and thermal-radiation-shielding textile woven with polyurethane (PU)-tin oxide (SnO2) composite microtubes, serving as an IR invisibility cloak, IR and thermal radiation emitted from the person or object can be simultaneously blocked. Furthermore, the IR- and thermal-radiation-shielding characteristics could be improved further by filling the core of the PU-SnO2 composite microtubes with heat-absorbing materials such as water and paraffin oil in place of air. In addition, the external surface of the IR- and thermal-radiation-shielding textile serving as an IR-reflecting cloak can be waterproofed to enable certain IR- and thermal-radiation-shielding functions under various environmental conditions.

Oxygen release from metal oxide for repeated hydrogen regeneration by proton irradiation with polyvinylpyrrolidone.

In this study, we investigated the reduction of a 3D microporous NiO x structure, used as a metal oxide catalyst, by proton irradiation with polyvinylpyrrolidone (PVP) for hydrogen regeneration. In general, the reduction process for hydrogen regeneration requires high temperatures (1000-4000 °C) to release saturated oxygen from the metal oxide catalyst. Proton irradiation with PVP could regenerate abundant oxygen vacancies by releasing the oxygen attached to NiO x at room temperature. The 3D microporous NiO x structure provided the maximum hydrogen generation rate of ∼4.2 µmol min-1 g-1 with the total amount of generated hydrogen being ∼460 µmol g-1 even in the repetitive thermochemical cycle; these results are similar to the initial hydrogen generation data. Therefore, continuous regeneration of hydrogen from the oxygen-reduced 3D microporous NiO x structure was possible. It is expected that the high thermal energy, which is the major problem associated with hydrogen regeneration through the conventional heat treatment method, would be resolved in future using such a method.

Continuous hydrogen regeneration through the oxygen vacancy control of metal oxides using microwave irradiation.

The amount of hydrogen gas generated from metal oxide materials, based on a thermochemical water-splitting method, gradually reduces as the surface of the metal oxide oxidizes during the hydrogen generation process. To regenerate hydrogen, the oxygen reduction process of a metal oxide at high temperatures (1000-2500 °C) is generally required. In this study, to overcome the problem of an energy efficiency imbalance, in which the required energy of the oxygen reduction process for hydrogen regeneration is higher than the generated hydrogen energy, we investigated the possibility of the oxygen reduction of a metal oxide with a low energy using microwave irradiation. For this purpose, a macroporous nickel-oxide structure was used as a metal oxide catalyst to generate hydrogen gas, and the oxidized surface of the macroporous nickel-oxide structure could be reduced by microwave irradiation. Through this oxidation reduction process, ∼750 µmol g-1 of hydrogen gas could be continuously regenerated. In this way, it is expected that oxygen-enriched metal oxide materials can be efficiently reduced by microwave irradiation, with a low power consumption of <∼4% compared to conventional high-temperature heat treatment, and thus can be used for efficient hydrogen generation and regeneration processes in the future.

Correlation of foot posture index with plantar pressure and radiographic measurements in pediatric flatfoot.

OBJECTIVE: To investigate the correlation between the Foot Posture Index (FPI) (including talar head palpation, curvature at the lateral malleoli, inversion/eversion of the calcaneus, talonavicular bulging, congruence of the medical longitudinal arch, and abduction/adduction of the forefoot on the rare foot), plantar pressure distribution, and pediatric flatfoot radiographic findings. METHODS: Nineteen children with flatfoot (age, 9.32±2.67 years) were included as the study group. Eight segments of plantar pressure were measured with the GaitView platform pressure pad and the FPI was measured in children. The four angles were measured on foot radiographs. We analyzed the correlation between the FPI, plantar pressure characteristics, and the radiographic angles in children with flatfoot. RESULTS: The ratio of hallux segment pressure and the second through fifth toe segment pressure was correlated with the FPI (r=0.385, p=0.017). The FPI was correlated with the lateral talo-first metatarsal angle (r=0.422, p=0.008) and calcaneal pitch (r=-0.411, p=0.01). CONCLUSION: Our results show a correlation between the FPI and plantar pressure. The FPI and pediatric flatfoot radiography are useful tools to evaluate pediatric flatfoot.

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) cm(2)/(V s) and an on/off ratio exceeding 1 × 10(4). 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.

Effects of the surface treatment with monolayers of twisted biaryls on the efficiency of pentacene thin-film transistors.

A pentacene thin-film transistor (TFT) was fabricated on a SiO2 gate insulator modified with twisted biaryls. The biaryl monolayer, in particular a binaphthyl (BN) monolayer, is amorphous surface where the naphthalene rings are randomly oriented with no lateral order because of their rigid, twisted, and asymmetric shape. When the BN monolayer was used for the surface treatment of SiO2, large grains were obtained in the early stages of the pentacene crystal growth. The pentacene TFT had a field effect mobility (microm) in excess of 0.4 cm2/Vs and an on/off ratio greater than 10(5). The surface treatment improved the mobility of the pentacene TFT by a factor of 50% compared with non-treated devices. The morphology of the semiconductor layer was investigated using atomic force microscopy (AFM) and X-ray diffraction (XRD).

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.

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.