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Vertically layered capacitive electrodes within a single sheet of paper are realized by using the hydrophobic barrier in the paper.

The composite material, Ag/AgX/graphene (X=Br, Cl, I), is considered a promising photocatalyst for photocatalytic degradation of organic pollutants. Its photocatalytic activity is superior to that of the conventional TiO2 photocatalyst; the enhanced photocatalytic activity is attributed to its effective charge separation ability and wide visible light absorption. However, the Ag/AgX/graphene composite is often prepared in the powder form, limiting its wide-spread application. In addition, the simple fabrication of Ag/AgX/graphene composite films is highly challenging. In this study, a simple solution-based process based on meniscus-dragging deposition is demonstrated for the fabrication of Ag/AgI/rGO composite films. Uniform catalyst films with reasonable photocatalytic activities can be easily fabricated by using this microliter-scale solution process.

Carbon nanotubes (CNTs) have received substantial attention as alternatives to indium tin oxide for the production of transparent conductors. However, problems associated with the dewetting of liquid thin films have hindered the reliable fabrication of networked conducting CNT films via solution-based processes. In this study, the dewetting of liquid thin films containing single-walled carbon nanotubes (SWCNTs) on substrates is successfully retarded by simply adding ethylene glycol to the SWCNT dispersion, and highly uniform SWCNT thin films are obtained using the meniscus-dragging deposition (MDD) method. The dewetting-free coating conditions for the uniform SWCNT films are determined by calculating the dewetting and drying times of the liquid thin films formed by the MDD method. When the dewetting time was 2.5 times longer than the drying time of the liquid thin layers, uniform SWCNT films are formed over the entire substrates without breakage or rupture of the films. In addition, the transmittance and sheet resistance of the transparent SWCNT films are easily controlled over a wide range by varying the coating parameters.

In this study, adhesion improved silver nanowires (AgNWs) conducting film was produced via the meniscus dragging deposition method. In order to improve adhesion of AgNWs films, the AgNWs were surface-modified with (3-aminopropyl)triethoxysilane (APTES) and coated over the pristine AgNWs networked film. Based on this strategy, the positively charged amine groups of the APTES-AgNWs and the negatively charged hydroxyl groups of the substrates formed electrostatic bonds, improving the adhesion between the AgNWs and substrates without sacrificing conductivity. AgNWs films on the rigid and flexible substrates were characterized using various analytical techniques. AgNWs networked film exhibited a sheet resistance of 6–22 Ω/sq at the transmittance at 550 nm, corresponding to 74–86% transmittance, confirming promising transparent electrodes. Adhesion of AgNWs film is confirmed based on a peel-off test and AgNWs film maintained a good conductivity even after several peel-off tests.

Metal mesh is a promising material for flexible transparent conducting electrodes due to its outstanding physical and electrical properties. The excellent control of the sheet resistance and transmittance provided by the metal mesh electrodes is a great advantage for microelectronic applications. Thus, over the past decade, many studies have been performed in order to realize high-performance metal mesh; however, the lack of cost-effective fabrication processes and the weak adhesion between the metal mesh and substrate have hindered its widespread adoption for flexible optoelectronic applications. In this study, a new approach for fabricating robust silver mesh without using hazardous organic solvents is achieved by combining colloidal deposition and silver enhancement steps. The adhesion of the metal mesh was greatly improved by introducing an intermediate adhesion layer. Various patterns relevant to optoelectronic applications were fabricated with a minimum feature size of 700 nm, resulting in high optical transmittance of 97.7% and also high conductivity (71.6 Ω sq

Capacitive sensors have been studied for various purposes, including detecting touch, pressure, and physical motions. However, a complicated process involving numerous electrode pattern arrays is necessary to detect touch positions. Here, a simply configured capacitive sensor with a single-layer ion gel (SIG) layer and copper electrodes without electrode arrays is reported. The touch sensor with a SIG is capable of precise touch sensing and touch positioning. The SIG touch sensor can detect the touch position by variation of the electric field in the ion gel layer and the change of the capacitance created by the touching object. Such a capacitive touch system has fast and accurate touch sensing capabilities and is independent of touch pressure. In addition, the touch sensor enables dynamic moving touch detection even when attached to the back of the human hand. Furthermore, an epidermal touch keypad is demonstrated by fabricating an array of three SIG touch sensors. The proposed capacitive touch sensor based on a SIG can enable the development of future electronic devices such as wearable electronics, soft robotics, electronic skin, and human–machine interaction systems.

We present a novel approach to produce high-resolution reduced graphene oxide (rGO) micropatterns based on a dewetting phenomenon of liquid thin films. The uniform liquid thin film of aqueous graphene oxide (GO) dispersion was formed by the meniscus dragging deposition method on a pre-patterned silanized substrate. Subsequently, selective dewetting of the water layer was induced due to the surface energy gradient on the coating substrates. After drying and chemical reduction, the high-resolution rGO micropatterns with a minimum feature size of 10 μm were realized over a large area substrate by consuming less than 1 μL of GO solution per square centimeter. As a demonstration of the application of this patterning technique, we have successfully fabricated organic field-effect transistors (OFETs) based on rGO pattern arrays as source–drain electrodes. The OFETs with the rGO electrodes exhibited a field effect mobility of 0.6 cm2 (V s)−1 with an on/off ratio of 1.79 × 106, which is higher than that of the devices with Au source–drain contacts.

This paper introduces composite microfibers that can distinguish liquid, normal, aliphatic alcohols with high selectivity. The composite microfibers are composed of a hydrophilic agarose polymer and carbon nanotube (CNT) fillers. The CNTs distributed in the CNT-agarose composite microfiber (CAF) enable the material to sensitively change its electrical conductivity upon exposure to alcohols, induced by a change in the volume of the polymer matrix. When a CAF is highly hydrated, its resistance distinctly changes depending on the molecular weight of the alcohol via competitive mass transfer of alcohol and water. As a result, highly hydrated CAFs can selectively distinguish normal, aliphatic alcohols ranging from methanol to 1-pentanol. A provisional mechanism for the alcohol-dependent change in resistance of hydrated CAFs is suggested based on the permeation of alcohols and the discharge of water and is supported by numerical calculations using a simple diffusion model. The effects of the CNT loading ratio and the as-prepared CAF diameter on the alcohol-dependent resistance change are investigated. Furthermore, the highly hydrated CAFs are used to determine the volume ratios of binary mixtures of methanol/ethanol and ethanol/water. Finally, we demonstrate that a CAF alcohol sensor can identify commercial liquors with different alcohol contents.

Oil/water microencapsulation by microfluidic systems has been a prominent delivery method to prepare functional microcapsules in the food, cosmetic, and pharmaceutical industries because it is an easy way to control the shape and size of structures and functionalities. We prepared biocompatible and multi-component microcapsules using the precipitation and ionic crosslinking of pectin in a poor solubility environment and with multivalent cations, respectively. When the aqueous solution (including calcium ions and ethanol) in a sheath flow met the flow of a pectin aqueous solution containing oil droplets, ethanol-gelation and ionic cross-linking occurred, enclosing the inner oil phase droplets by solidified pectin shells. Furthermore, the resulting microcapsules stabilized by pectin shells exhibited functionalities using a hydrophobic agent and nanoparticles of a hydrophilic species that were dissolved and dispersed, respectively, in the oil phase.

Strain sensor technologies have been spotlighted for their versatility for healthcare, soft robot, and human–robot applications. Expecting large future demands for such technology, extensive studies have investigated flexible and stretchable strain sensors based on various nanomaterials and metal films. However, it is still challenging to simultaneously satisfy parameters such as sensitivity, stretchability, linearity, hysteresis, and mass producibility. In this work, we demonstrate a novel approach for producing highly sensitive metal-grid strain sensors based on an all-solution process, which is suitable for mass production. We investigated the effects of the width of the metal grid and width/spacing ratio on the piezoresistivity of the strain sensors. The metal grid strain sensors exhibited high sensitivity (gauge factor of 4685.9 at 5% strain), rapid response time (∼18.6 ms), and superior strain range (≤5%) compared to other metal-based sensors. We demonstrated that the sensors could successfully convert voice signals and tiny movements of fingers and muscles into electrical signals. In addition, the metal-grid strain sensors were produced using a low-cost procedure without toxic solvent via an all water-based solution process, which is expected to allow the integration of such metal-grid strain sensors into future highly sensitive physical sensing devices.

Curved Cu nanowire (CCN)-based high-performance flexible transparent conductive electrodes (FTCEs) were fabricated via a fully solution-processed approach, involving synthesis, coating, patterning, welding, and transfer. Each step involved an innovative technique for completing the all-solution processes. The high-quality and well-dispersed CCNs were synthesized using a multi-polyol method through the synergistic effect of specific polyol reduction. To precisely control the optoelectrical properties of the FTCEs, the CCNs were uniformly coated on a polyimide (PI) substrate via a simple meniscus-dragging deposition method by tuning several coating parameters. We also employed a polyurethane (PU)-stamped patterning method to effectively produce 20 μm patterns on CCN thin films. The CCN thin films exhibited high electrical performance, which is attributed to the deeply percolated CCN network formed via a solvent-dipped welding method. Finally, the CCN thin films on the PI substrate were partially embedded and transferred to the PU matrix to reduce their surface roughness. Through consecutive processes involving the proposed methods, a highly percolated CCN thin film on the PU matrix exhibited high optoelectrical performance (R s = 53.48 Ω/□ at T = 85.71%), excellent mechanical properties (R/R 0 < 1.10 after the 10th repetition of tape peeling or 1,000 bending cycles), and a low root-mean-square surface roughness (R rms = 14.36 nm).

We present a simple liquid-type strain sensor using a binary mixture of ethylene glycol (EG) and ionic liquid (IL) in a linear microfluidic channel. The EG/IL-based strain sensor showed highly sensitive response to tensile strain in a polydimethylsiloxane (PDMS) microfluidic channel. In addition, the EG/IL-based strain sensor exhibited outstanding signal recovery and high sensitivity to applied strain (200%) in an Eco-Flex microfluidic channel. The EG/IL-based strain sensor exhibited 2.3 times higher gauge factor at 200% strain, compared to the microfluidic strain sensor using neat IL. Moreover, the EG/IL strain sensor showed clear signal responses with negligible hysteresis, even at high strain speed of 16.667 mm/s. Compared to other liquid-type strain sensors, the EG/IL-based strain sensor exhibited very high resistance variations, surpassing the elastic channel deformation effect. To explain this effect, the conducting behavior of ionic liquids in ethylene glycol was also investigated. This novel fabrication of EG/IL-based strain sensors shows potential for the development and practical application of liquid-type strain sensors.

We report a new class of simple fluidic capacitive sensors based on microfluidic techniques, which are capable of multimodal sensing performances. The microfluidic multifunctional capacitive sensors were realized by using ionic liquids acting as electrodes in microchannels and a CNT/PDMS composite as a dielectric layer. Our microfluidic capacitive sensors offer outstanding sensor performance to detect localized pressure and even lateral pressure variation as well as ambient temperature changes. The principle of our new microfluidic capacitive sensors is explained by the electric double layer capacitance and the ion distribution along the ionic liquid electrodes. In order to demonstrate their capability for practical usage, our simple structured microfluidic capacitive sensors were applied to a bottle and human skin for monitoring the variation of pressure and temperature simultaneously. The highly sensitive microfluidic capacitive sensors were successfully applied as keypads and potential platforms for distinctively detecting various hand or finger motions such as tapping, scratching, and stacking. Our novel microfluidic multimodal capacitive sensors show great promise for making future stretchable electronic devices, such as wearable electronics, soft robotics, and artificial skin.

A new random copolymer consisting of similarly shaped donor-acceptor building blocks of diketopyrrolopyrrole-selenophene-vinylene-selenophene (DPP-SVS) and DPP-thiophene-vinylene-thiophene (DPP-TVT) is designed and synthesized. The resulting P-DPP-SVS(5)-TVT(5) with an equal molecular ratio of the two building blocks produced significantly enhanced solubility when compared to that of the two homopolymers, PDPP-SVS and PDPP-TVT. More importantly, despite the maximum segmental randomness of the PDPP-SVS(5)-TVT(5) copolymer, its crystalline perfectness and preferential orientation are outstanding, even similar to those of the homopolymers thanks to the similarity of the two building blocks. This unique property produces a high charge carrier mobility of 1.23 cm2 V-1 s-1 of PDPP-SVS(5)-TVT(5), as determined from polymer field-effect transistor (PFET) measurements. The high solubility of PDPP-SVS(5)-TVT(5) promotes formulation of high-viscosity solutions which could be successfully processed to fabricate large-areal PFETs onto hydrophobically treated 4 in. wafers. A total of 269 individual PFETs are fabricated. These devices exhibit extremely narrow device-to-device deviations without a single failure and demonstrate an average charge carrier mobility of 0.66 cm2 V-1 s-1 with a standard deviation of 0.064. This is the first study to report on successfully realizing large-areal reproducibility of high-mobility polymeric semiconductors.

A conjugated polymer, poly(9,9-bis(6-bromohexyl)-9H-fluorene-alt-1,4-phenylene), is synthesized, converted to nanoparticles via a nanoprecipitation process, and utilized to fabricate thin films including conjugated polymer nanoparticles. The nanoparticles with surface bromides can be conjugated with an amine-functionalized dendrimer via a nucleophilic coupling reaction. Thus, when microliter solutions of the particulates are dragged at a constant velocity on substrates alternately in a layer-by-layer manner, thin films composed of the nanoparticles and dendrimers can be successfully built up on the substrates. Our results suggest a methodology to control the deposition of thin films bearing conjugated polymer nanoparticles while minimizing processing time and decreasing material consumption.

Transparent conducting electrodes (TCEs) formed with silver nanowires (AgNWs) have attracted attention as substitutes for indium tin oxide (ITO). However, the randomly deposited AgNW film performs poorly in terms of the transmittance and sheet resistance to serve as a substitute of ITO. To improve the performance of the AgNW film, we fabricated a grid-patterned AgNW by modifying the surface energy of the substrate. The hydrophobized surface was selectively etched by UV light through a quartz chrome mask, and a suspension of AgNWs in isopropyl alcohol/ethylene glycol mixture was coated on the substrate by a meniscus dragging deposition process. The grid-patterned AgNW film has a lower percolation threshold and a 13% higher figure-of-merit value compared to the randomly deposited AgNW film. The transparent thin films with a grid structure of AgNWs exhibit the high electrical conductivity with a sheet resistance of 33 Ohm/sq at a transmittance of 92.7% (&lambda, = 550 nm).

Strain sensor technologies have been spotlighted for their versatility for healthcare, soft robot, and human-robot applications. Expecting large future demands for such technology, extensive studies have investigated flexible and stretchable strain sensors based on various nanomaterials and metal films. However, it is still challenging to simultaneously satisfy parameters such as sensitivity, stretchability, linearity, hysteresis, and mass producibility. In this work, we demonstrate a novel approach for producing highly sensitive metal-grid strain sensors based on an all-solution process, which is suitable for mass production. We investigated the effects of the width of the metal grid and width/spacing ratio on the piezoresistivity of the strain sensors. The metal grid strain sensors exhibited high sensitivity (gauge factor of 4685.9 at 5% strain), rapid response time (∼18.6 ms), and superior strain range (≤5%) compared to other metal-based sensors. We demonstrated that the sensors could successfully convert voice signals and tiny movements of fingers and muscles into electrical signals. In addition, the metal-grid strain sensors were produced using a low-cost procedure without toxic solvent

In this work, a whole manufacturing process of the curved copper nanowires (CCNs) based flexible transparent conductive electrode (FTCE) is reported with all solution processes, including synthesis, coating, and networking. The CCNs with high purity and good quality are designed and synthesized by a binary polyol coreduction method. In this reaction, volume ratio and reaction time are the significant factors for the successful synthesis. These nanowires have an average 50 nm in width and 25-40 μm range in length with curved structure and high softness. Furthermore, a meniscus-dragging deposition (MDD) method is used to uniformly coat the well-dispersed CCNs on the glass or polyethylene terephthalate substrate with a simple process. The optoelectrical property of the CCNs thin films is precisely controlled by applying the MDD method. The FTCE is fabricated by networking of CCNs using solvent-dipped annealing method with vacuum-free, transfer-free, and low-temperature conditions. To remove the natural oxide layer, the CCNs thin films are reduced by glycerol or NaBH4 solution at low temperature. As a highly robust FTCE, the CCNs thin film exhibits excellent optoelectrical performance (T = 86.62%, R(s) = 99.14 Ω ◻(-1)), flexibility, and durability (R/R(0) < 1.05 at 2000 bending, 5 mm of bending radius).

We report on a new class of microliter-scale solution processes for fabricating highly uniform and large-area transistor arrays with extremely low consumption of semiconducting polymers. These processes are accomplished by applying a vertical phase separation of polymers with an environmentally benign solvent, a random copolymerization strategy between two highly conductive repeating units, and a meniscus-dragging deposition technique. The successful realization of these three processes, as confirmed by the structural and morphological in-depth characterizations, has enabled the fabrication of high-performance polymeric field-effect transistors that were uniformly distributed, without a single failure, on a 4 inch wafer using only 40 μg of semiconducting polymers. The resulting transistor arrays showed an average mobility of 0.28 cm2 V−1 s−1, with a low standard deviation of 0.04, as well as ultra-uniform near-zero threshold voltages. Our simple strategy shows great promise for fabricating large-scale organic electronic devices in the future using a truly low-cost process.

A microliter-scale solution process was used to fabricate large-area, uniform films of silver nanowires (AgNWs). These thin films with cross-AgNWs were deposited onto Au substrates by dragging the meniscus of a microliter drop of a coating solution trapped between two plates. The hot spot density was tuned by controlling simple experimental parameters, which changed the optical properties of the resulting films. The cross-AgNW films on the Au surface served as excellent substrates for surface-enhanced Raman spectroscopy, with substantial electromagnetic field enhancement and good reproducibility.

A new class of simple and highly sensitive piezocapacitive sensors that are capable of detecting static and dynamic pressure changes is reported. The pressure sensor structure is formed by vertically sandwiching a sandpaper-molded carbon nanotube/poly(dimethylsiloxane) composite (CPC) dielectric layer between two ion-gel thin film electrodes. Such a capacitive sensor system enables the distinguishable detection of directional movement of applied pressure as well as static pressure variation by modulating ion distribution in the ion-gel thin films. The resulting capacitive pressure sensors exhibit high sensitivity (9.55 kPa–1), high durability, and low operating voltage (0.1 V). Our proposed pressure sensors are successfully applied as potential platforms for monitoring human physiological signals and finger sliding motions in order to demonstrate their capability for practical usage. The outstanding sensor performance of the pressure sensors can permit applications in wearable electronic devices for human...

Retinyl palmitate (RP)-loaded pectinate micro- and nano-particles (PMP and PNP) were designed for stabilization of RP that is widely used as an anti-wrinkle agent in anti-aging cosmeceuticals. PMP/PNP were prepared with an ionotropic gelation method, and anti-oxidative activity of the particles was measured with a DPPH assay. The stability of RP in the particles along with pectin gel and ethanolic solution was then evaluated. In vitro release and skin permeation studies were performed using Franz diffusion cells. Distribution of RP in each skin tissue (stratum corneum, epidermis, and dermis) was also determined. PMP and PNP could be prepared with mean particle size diameters of 593~843 μm (PMP) and 530 nm (i.e., 0.53 μm, PNP). Anti-oxidative activity of PNP was greater than PMP due largely to larger surface area available for PNP. The stability of RP in PMP and PNP was similar but much greater than RP in pectin bulk gels and ethanolic solution. PMP and PNP showed the abilities to constantly release RP and it could be permeated across the model artificial membrane and rat whole skin. RP was serially deposited throughout the skin layers. This study implies RP loaded PMP and PNP are expected to be advantageous for improved anti-wrinkle effects.

We report the simple production of highly uniform single-walled carbon nanotube (SWCNT) thin films with significant reduction of the conducting material consumption by applying an effective microliter-scale solution process. The transparent thin film conductors were formed directly on a rigid or flexible substrate within a short process time by dragging a meniscus of an aqueous SWCNT solution with a volume of tens of microliters. The easily controllable coating parameters enabled the fine-tuning of the film thickness on a nanometer scale. This coating process is well suited for large-area, bendable SWCNT thin films whose randomly interconnected networks exhibit two-dimensional percolation behavior.

We demonstrated the solution-processed single-walled carbon nanotube (SWNT) source-drain electrodes patterned using a plasma-enhanced detachment patterning method for high-performance organic transistors and inverters. The high-resolution SWNT electrode patterning began with the formation of highly uniform SWNT thin films on a hydrophobic silanized substrate. The SWNT source-drain patterns were then formed by modulating the interfacial energies of the prepatterned elastomeric mold and the SWNT thin film using oxygen plasma. The SWNT films were subsequently selectively delaminated using a rubber mold. The patterned SWNTs could be used as the source-drain electrodes for both n-type PTCDI-C8 and p-type pentacene field-effect transistors (FETs). The n- and p-type devices exhibited good and exactly matched electrical performances, with a field-effect mobility of around 0.15 cm(2) V(-1) s(-1) and an ON/OFF current ratio exceeding 10(6). The single electrode material was used for both the n and p channels, permitting the successful fabrication of a high-performance complementary inverter by connecting a p-type pentacene FET to an n-type PTCDI-C8 FET. This patterning technique was simple, inexpensive, and easily scaled for the preparation of large-area electrode micropatterns for flexible microelectronic device fabrication.

This study presents a new DEP manipulation technique using a movable liquid electrode, which allows manipulation of particles by actively controlling the locations of electrodes and applying on-off electric input signals. This DEP system consists of mercury as a movable liquid electrode, indium tin oxide (ITO)-coated glass, SU-8-based microchannels for electrode passages, and a PDMS medium chamber. A simple squeezing method was introduced to build a thin PDMS layer at the bottom of the medium chamber to create a contactless DEP system. To determine the operating conditions, the DEP force and the friction force were analytically compared for a single cell. In addition, an appropriate frequency range for effective DEP manipulation was chosen based on an estimation of the Clausius-Mossotti factor and the effective complex permittivity of the yeast cell using the concentric shell model. With this system, we demonstrated the active manipulation of yeast cells, and measured the collection efficiency and the dielectrophoretic velocity of cells for different AC electric field strengths and applied frequencies. The experimental results showed that the maximum collection efficiency reached was approximately 90%, and the dielectrophoretic velocity increased with increasing frequency and attained the maximum value of 10.85 ± 0.95 μm/s at 100 kHz, above which it decreased.

In this study, we report a simple and effective process for the fabrication of wrinkle structures of chemically derived graphene thin films and patterns. Reduced graphene oxide (rGO) thin films/patterns formed on glass substrates are transferred to pre-strained elastomeric layers by improving adhesion strength at the rGO/PDMS interface with the assistance of oxygen plasma treatment. The morphology of rGO wrinkle structures is investigated in the various applied strains and film thicknesses. The experimental results were interpreted by theoretical models and well fitted to the estimated values. The techniques for such well-defined rGO wrinkle structures could be used for flexible and stretchable graphene-based electronic devices.

Electrochemical reduction for conversion of CO2 to value-added chemicals is considered a promising method to relieve global warming. To develop a highly active and selective electrocatalyst for efficient CO2 conversion, it is essential to overcome the large overpotential and to suppress the competitive hydrogen evolution reaction (HER). Herein, we report a simple and controllable fabrication method for Ag electrocatalytic films using all-water-based solution processes via a seed-meditated metal growth technique. Varying the deposition conditions allows the N/S doping ratio in Ag films with high coverage and good adhesion to be easily controlled in the range of 1.14–8.23. The doping ratio has a significant effect on the CO Faradaic efficiency (FE), as the S content modulates the binding energy of reaction intermediates, whereas the N content is effective for suppressing the HER on the Ag film surface.

We performed oxygen plasma treatment on reduced graphene oxide (rGO) to improve its surface reactivity with respect to biomolecular interactions. Oxygen-plasma-treated rGO surfaces were employed as reactive interfaces for the detection of amyloid-beta (Aβ) peptides, the pathological hallmarks of Alzheimer's disease (AD), as the target analytes. By measuring the changes in electrical characteristics and confirmation through topographic analysis, the oxygen-plasma-treated rGO sensors had enhanced surface functionality for better antibody immobilization and sensing performance, with a 3.33-fold steeper slope for the electrical responses versus analyte concentration curve (logarithmic scale) compared to the untreated. The elicited biomolecular reactivity of the rGO surfaces with the oxygen plasma treatment remained at 46-51% of the initial value even after aging for 6h in ambient conditions. This phenomenon was also confirmed by pretreating the rGO surfaces with a blocking agent and subsequently subjecting them to antibody immobilization. Finally, the feasibility of the oxygen-plasma-treated rGO sensors as a diagnostic tool was evaluated with clinical samples of neural-derived exosomal Aβ peptides extracted from apparent AD patients and normal controls (NC). In contrast to the untreated sensors (p=0.0460), the oxygen-plasma-treated rGO sensors showed a significant p-value in the identification of clinical samples of AD and NC subjects (p

We present a class of gel-based self-propelling particles moving by the Marangoni effect in an oscillatory mode. The particles are made of an ethanol-infused polyacrylamide hydrogel contained in plastic tubing. These gel boats floating on the water surface exhibit periodic propulsion for several hours. The release of ethanol from the hydrogel takes place beneath the liquid surface. The released ethanol rises to the air-water interface by buoyancy and generates a self-sustained cycle of surface tension gradient driven motion. The disruption of the ethanol flux to the surface by the bulk flows around the moving particle results in their pulsating motion. The pulse interval and the distance propelled in a pulse by these gel floaters were measured and approximated by simple expressions based on the rate of ethanol mass-transfer through and out of the hydrogel. This allowed us to design a multitude of particles performing periodic steps in different directions or at different angles of rotation, traveling in complex preprogrammed trajectories on the surface of the liquid. Similar gel-based self-propelling floaters can find applications as mixers and cargo carriers in lab-on-a-chip devices, and in various platforms for sensing and processing at the microscale.

Exposure of mammalian cells to oxidative stress alters lysosomal enzymes. Through cytochemical analysis of lysosomes with LysoTracker, we demonstrated that the number and fluorescent intensity of lysosome-like organelles in HeLa cells increased with exposure to hydrogen peroxide (H₂O₂), 6-hydroxydopamine (6-OHDA), and UVB irradiation. The lysosomes isolated from HeLa cells exposed to three oxidative stressors showed the enhanced antimicrobial activity against Escherichia coli. Further, when lysosomes that were isolated from HeLa cells exposed by oxidative stress were treated to normal HeLa cells, the viability of the HeLa cells was drastically reduced, suggesting increased in vitro lysosomal function (i.e., antimicrobial activity, apoptotic cell death). In addition, we also found that cathepsin B and D were implicated in increased in vitro lysosomal function when isolated from HeLa cells exposed by oxidative stress. Decrease in cathepsin B activity and increase in cathepsin D activity were observed in lysosomes isolated from HeLa cells after treatment with H₂O₂, 6-ODHA, or UVB, but cathepsin B and D were not the sole factors to induce cell death by in vitro lysosomal function. Therefore, these studies suggest a new approach to use lysosomes as antimicrobial agents and as new materials for treating cancer cell lines.

Rhodobacter sphaeroides is a purple non-sulfur photosynthetic bacteria that participates in the anoxic cycling of carbon both as the primary producer and as the light-stimulated consumers of the reduced organic compounds. In this study, six different organic acids, i.e. acetate, lactate, oxaloacetate, malate, succinate, and citrate, were selected and used to analyze the relationships between the organic acid source and the cell growth. The C4 compound exhibited an enhanced cell growth compared to the other organic acids, and the growth rate of R. sphaeroides that was grown with 0.03 M succinic acid was significantly 3.2-fold faster than the C6 compound of 0.03 M citrate. Additionally, the cell growth of R. sphaeroides was enhanced with increasing light intensity, and the growth rate and the dry cell weight of R.sphaeroides that were grown under the light conditions of 15 W/m2 were 2.0- and 1.2-fold higher than R. sphaeroides at 3 W/m2. Therefore, the high light intensity probably affected the growth of R. sphaeroides. Moreover, the blue-colored light emitting diode (LED) exhibited a highest growth rate and cell concentration of R. sphaeroides among the various types of LEDs, and the enhanced cell growth phenomenon under the blue LED conditions was dramatically stimulated at low concentrations of succinic acid, which was compensatory for succinic acid. Therefore, a high light intensity and a blue LED as the light source were necessary for the enhanced cell growth for the C4 organic acid, i.e. succinic acid.

Microsensors and micromachines that are capable of self-propulsion through fluids could revolutionize many aspects of technology. Few principles to propel such devices and supply them with energy are known. Here, we show that various types of miniature semiconductor diodes floating in water act as self-propelling particles when powered by an external alternating electric field. The millimetre-sized diodes rectify the voltage induced between their electrodes. The resulting particle-localized electro-osmotic flow propels them in the direction of either the cathode or the anode, depending on their surface charge. These rudimentary self-propelling devices can emit light or respond to light and could be controlled by internal logic. Diodes embedded in the walls of microfluidic channels provide locally distributed pumping or mixing functions powered by a global external field. The combined application of a.c. and d.c. fields in such devices allows decoupling of the velocity of the particles and the liquid and could be used for on-chip separations.

We report an effective method for fabricating highly transparent and stretchable large-area conducting films based on a directional arrangement of silver nanowires (AgNWs) driven by a shear force in a microliter-scale solution process. The thin conducting films with parallel AgNWs or cross-junctions of AgNWs are deposited on the coating substrate by dragging a microliter drop of the coating solution trapped between two plates. The optical and electrical properties of the AgNW thin films are finely tuned by varying the simple systematic parameters in the coating process. The transparent thin films with AgNW cross-junctions exhibit the superior electrical conductivity with a sheet resistance of 10 Ω sq(-1) at a transmittance of 85% (λ = 550 nm), which is well described by the high ratio of DC to optical conductivity of 276 and percolation theory in a two-dimensional matrix model. This simple coating method enables the deposition of AgNW thin films with high optical transparency, flexibility, and stretchability directly on plastic substrates.

We report a new class of simple microfluidic strain sensors with high stretchability, transparency, sensitivity, and long-term stability with no considerable hysteresis and a fast response to various deformations by combining the merits of microfluidic techniques and ionic liquids. The high optical transparency of the strain sensors was achieved by introducing refractive-index matched ionic liquids into microfluidic networks or channels embedded in an elastomeric matrix. The microfluidic strain sensors offer the outstanding sensor performance under a variety of deformations induced by stretching, bending, pressing, and twisting of the microfluidic strain sensors. The principle of our microfluidic strain sensor is explained by a theoretical model based on the elastic channel deformation. In order to demonstrate its capability of practical usage, the simple-structured microfluidic strain sensors were performed onto a finger, wrist, and arm. The highly stretchable and transparent microfluidic strain sensors were successfully applied as potential platforms for distinctively monitoring a wide range of human body motions in real time. Our novel microfluidic strain sensors show great promise for making future stretchable electronic devices.

A one-step, template-free synthetic method for preparing polymeric microcapsules with iron oxide (A-Fe2O3) magnetic nanoparticles (MPs) embedded in the polymer shell is reported. Using a simple emulsification of the multiphase mixture containing liquid prepolymer and MPs in chloroform solution, double emulsions comprising a chloroform core and MPs/polymer shell were spontaneously formed. After exposure to UV light, these double emulsions converted to microcapsules with a polymerized composite shell. The evolution from the double emulsions to the microcapsules was examined by confocal laser scanning microscopy. One unusual feature of these microcapsules is the ability to change shape reversibly by osmotic swelling of the water core upon repetitive drying and hydration. The microcapsules had an intrinsic superparamagnetic response due to the presence of the magnetic nanoparticles and could be moved and collected by external magnetic fields.

We describe phenomena of colloidal particle transport and separation inside single microdroplets of water floating on the surface of dense fluorinated oil. The experiments were performed on microfluidic chips, where single droplets were manipulated with alternating electric fields applied to arrays of electrodes below the oil. The particles suspended in the droplets were collected in their top region during the evaporation process. Experimental results and numerical simulations show that this microsepration occurs as a result of a series of processes driven by mass and heat transfer. An interfacial tension gradient develops on the surface of the droplet as a result of the nonuniform temperature distribution during the evaporation. This gradient generates an internal convective Marangoni flow. The colloidal particles transported by the flow are collected in the top of the droplets by the hydrodynamic flux, compensating for evaporation through the exposed top surface. The internal flow pattern and temperature distribution within evaporating droplets were simulated using finite element calculations. The results of the simulation were consistent with experiments using tracer particles. Such microseparation processes can be used for on-chip synthesis of advanced particles and innovative microbioassays.

Cellulose-based microparticles are produced by changing the pH value adjacent to the interfaces between CO2 gas bubbles and an aqueous solution containing the pH-sensitive polymer hydroxypropyl met...

Hollow core polyacrylonitrile (PAN) microfibers with nano- and microporosity are synthesized based on the regeneration of PAN from dimethyl sulfoxide in a hydrodynamic flow-focusing microfluidic de...

A soil biosensor was developed in our previous study using both a recombinant bioluminescent bacterium, GC2 (lac::luxCDABE), immobilized with transparent glass beads within an agar matrix and rhamnolipids, a biosurfactant employed to increase the bioavailability of phenanthrene from contaminated soil. To improve the sensitivity of this biosensor, glass beads of various sizes were tested. The results showed that the detection limit of the biosensor was lowered when smaller-sized glass beads were employed. Further tests showed that the use of glass beads with smaller diameters enhanced the sensitivity of the biosensor, allowing for a more conclusive study on the phenanthrene toxicity present within soils.