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As transparent, flexible, and wearable organic electronics degrade under normal outdoor environmental conditions (e.g., water vapor, oxygen, and UV light) and extreme environments, including washing or rain, a customized encapsulation technology is required to improve device reliability. Herein, a simple process is presented for fabricating multifunctional hazy substrates (MFHSs) with excellent gas diffusion barrier (GDB), flexibility, UV reflectance, light scattering, and waterproof properties. First, a spiky polyethylene terephthalate (PET) surface is produced with 76.0% optical haze through ion‐beam treatment followed by the formation of a hydrophobic layer to achieve a waterproof effect (contact angle: 153.3°). Then, a multifunctional multibarrier film is fabricated based on a nano‐laminated distributed Bragg reflector and functional polymer on the functional PET substrate to serve as a GDB and UV filter. This multibarrier film has excellent mechanical and chemical stabilities, in addition to having a water vapor transmission rate of 10−6 g m−2 day−1 and UV transmittance of <3%. The so‐fabricated MFHS not only increases the device efficiency by 73% but also enables a highly flexible and environmentally stable organic light–emitting diode. The surface treatment and encapsulation technologies developed in this study are expected to increase the lifetime of organic devices and facilitate high outdoor usability. [ABSTRACT FROM AUTHOR]

Electroporation is pivotal in bioelectrochemistry for cellular manipulation, with prominent applications in drug delivery and cell membrane studies. A comprehensive understanding of pore generation requires an in-depth analysis of the critical pore size and the corresponding energy barrier at the onset of cell rupture. However, many studies have been limited to basic models such as artificial membranes or theoretical simulations. Challenging this paradigm, our study pioneers using a microfluidic electroporation chip array. This tool subjects live breast cancer cell species to a diverse spectrum of alternating current electric field conditions, driving electroporation-induced cell rupture. We conclusively determined the rupture voltages across varying applied voltage loading rates, enabling an unprecedented characterization of electric cell rupture dynamics encompassing critical pore radius and energy barrier. Further bolstering our investigation, we probed cells subjected to cholesterol depletion via methyl-β-cyclodextrin and revealed a strong correlation with electroporation. This work not only elucidates the dynamics of electric rupture in live cell membranes but also sets a robust foundation for future explorations into the mechanisms and energetics of live cell electroporation. [ABSTRACT FROM AUTHOR]

Solid electrolytes (SEs) play an essential role in the development of all‐solid‐state batteries (ASSBs) due to their exceptional ionic conductivity. However, conventional pelletized SEs with hundreds of micrometers result in highly reduced energy density and suffer from mechanical brittleness, which delay the commercialization of ASSBs. In this study, we present an innovative approach to fabricate SE membranes with perforated Al2O3 nanolayer‐coated polyethylene (PE) separator as a mechanical supporter. Al2O3‐coated separators exhibit better adhesion with LPSCl particles and better thermal stability. As a result, the SE membrane exhibits thickness of 35 μm while maintaining a superior mechanical tensile strength. Furthermore, when the SE membrane is applied to Li||LiNi0.7Co0.15Mn0.15O2 full‐cells, stable cycling performance over 250 cycles, which is comparable to thick LPSCl pellet cell, can be achieved even with higher conductance (>150 mS). Our results highlight the potential of thin and durable SE membranes in contributing to the commercialization of ASSBs. [ABSTRACT FROM AUTHOR]

Recently, as state‐of‐the‐art displays, wearable electronic devices and free‐form displays have begun to attract attention to the point that much research on textile‐based displays has been actively conducted as an ultimate platform for wearable displays. However, although many studies have reported organic light‐emitting diodes (OLEDs) as the most suitable type for textile‐based displays due to their high opto‐electronic performance and flexibility, most research on textile‐based OLEDs (textile OLEDs) has left for the future improvements that require the use of transparent OLEDs (trOLEDs) for applications where aesthetics are important, such as fashion displays and automobile interiors. Herein, RGB‐color trOLEDs are designed using a dielectric‐metal‐dielectric transparent electrode to overcome the limitations of previous works on textile‐based non‐transparent OLEDs and to improve the aesthetic elements of textile displays. The opto‐electronic performance and the mechanical characteristics of textile RGB trOLEDs are analyzed, and specifically, this study suggests a new method and a novel equation for an optical analysis to quantify the clarity of printed color images (i.e., information) on a textile substrate when trOLEDs on the textile substrate are not operated, as needed to optimize and maximize the aesthetic elements of textile displays. [ABSTRACT FROM AUTHOR]

Neonatal jaundice is a very common disease in newborns and can lead to brain damage or death in severe cases. Phototherapy with light‐emitting diode (LED) arrays is widely used as the easiest and fastest way to relieve jaundice in newborns, but it has distinct disadvantages such as loss of water in the patient, damage to the retina, and separation from parents. In this paper, a novel light source‐based phototherapy for neonatal jaundice is proposed using a textile‐based wearable organic light‐emitting diode (OLED) platform that can move flexibly and conform to the curvature of the human body. The soft and flexible textile‐based blue OLED platform is designed to have a peak wavelength of 470 nm, suitable for jaundice treatment, and shows performance (>20 µW cm−2 nm−1) suitable for intensive jaundice treatment even at low voltage (<4.0 V). The textile‐based OLEDs fabricated in this study exhibit an operating reliability of over 100 h and low‐temperature operation (<35 °C). The results of an in vitro jaundice treatment test using a large‐area blue OLED confirm that the bilirubin level decreases to 12 mg dL−1 with 3 h of OLED irradiation. [ABSTRACT FROM AUTHOR]

Abstract: Photobiomodulation (PBM) is a safe and noninvasive method that can provide various clinical effects. However, conventional PBM devices using point light sources, such as light‐emitting diodes and lasers have various disadvantages, such as low flexibility, relatively heavy weight, and nonuniform effects. This paper presents a novel wearable PBM patch using a flexible red‐wavelength organic light‐emitting diode (OLED) surface light source, which can be attached to the human body as a personalized PBM platform. The palm‐sized wearable PBM patch can be very light (0.82 g) and thin (676 µm). It also has a reasonable operation life (>300 h), flexibility (20 mm bending radius), and low‐temperature operation (<40 °C), and it can provide wide and safe application irrespective of location and time. Fibroblasts, a major type of dermal cells, play a key role in the wound healing process. The results show that OLEDs may have excellent in vitro wound healing effects because they effectively stimulate fibroblast proliferation (over 58% of control) and enhance fibroblast migration (over 46% of control) under various conditions. For maximum effect, peak wavelength control is necessary to optimize cell proliferation and enhance in vivo wound healing effects. [ABSTRACT FROM AUTHOR]

We demonstrate a wearable photobiomodulation patch using attachable flexible organic light‐emitting diodes. These platforms are very thin (~1.1mm) and can be attached to any part of the body. In addition, by controlling the wavelength (630nm to 650nm), the keratinocyte wound‐healing promotion effect can be optimized by as much as 31.5%. [ABSTRACT FROM AUTHOR]

In this study, two types of PLEDs were utilized for an in‐vitro test to verify the effect of solution‐processed OLEDs on cell metabolic activity. As a result, there was no cytotoxicity on any of the irradiated fibroblast cells, and an improved cell proliferation effect of about 109% was obtained. [ABSTRACT FROM AUTHOR]

A clothing‐shaped substrate that matches the characteristics of a fabric was designed to minimize the physical strain and stress on organic light‐emitting diodes(OLEDs).The room temperature process minimized the deformation of the fabric during the fabrication process, and a clothing‐shaped substrate having the same surface as a flat glass substrate was fabricated. Finally, clothing‐shaped OLED that provide excellent wearing comfort such as clothes was proposed, and flexibility, bending and wrinkling characteristics were evaluated. [ABSTRACT FROM AUTHOR]

We demonstrated polymer light-emitting diodes (PLEDs) using the dip coating method on a flat glass and flat polyethylene terephthalate (PET) substrates as well as on a cylinder-shaped fiber substrate. This result enables the production of low-cost, easily fabricated flexible fiber-based PLEDs by roll-to-roll manufacturing as well as the realization of a true fiber-based wearable display. [ABSTRACT FROM AUTHOR]

Clothing‐type, textile‐based OLEDs and their bio‐medical application have been investigated. Textile‐based OLEDs have shown wide applicability and washability as well as high flexibility for a wearing textile displays. Furthermore, a novel phototherapy for neonatal jaundice by using textile‐OLEDs was proposed in this work. [ABSTRACT FROM AUTHOR]

Characterization of cellular dielectrophoretic (DEP) behaviors, when cells are exposed to an alternating current (AC) electric field of varying frequency, is fundamentally important to many applications using dielectrophoresis. However, to date, that characterization has been performed with monotonically increasing or decreasing frequency, not with successive increases and decreases, even though cells might behave differently with those frequency modulations due to the nonlinear cellular electrodynamic responses reported in previous works. In this report, we present a method to trace the behaviors of numerous cells simultaneously at the single-cell level in a simple, robust manner using dielectrophoretic tweezers-based force spectroscopy. Using this method, the behaviors of more than 150 cells were traced in a single environment at the same time, while a modulated DEP force acted upon them, resulting in characterization of nonlinear DEP cellular behaviors and generation of different cross-over frequencies in living cells by modulating the DEP force. This study demonstrated that living cells can have non-linear di-polarized responses depending on the modulation direction of the applied frequency as well as providing a simple and reliable platform from which to measure a cellular cross-over frequency and characterize its nonlinear property. [ABSTRACT FROM AUTHOR]

In recent years, an interesting biomarker called membrane breakdown voltage has been examined using artificial planar lipid bilayers. Even though they have great potential to identify cell electrical phenotyping for distinguishing similar cell lines or cells under different physiological conditions, the biomarker has not been evaluated in the context of living cell electrical phenotyping. Herein, we present a single-cell analysis platform to continuously measure the electric response in a large number of cells in parallel using electric frequency and voltage variables. Using this platform, we measured the direction of cell displacement and transparent cell image alteration as electric polarization of the cell responds to signal modulation, extracting the dielectrophoretic crossover frequency and membrane breakdown voltage for each cell, and utilizing the measurement results in the same spatiotemporal environment. We developed paired parameters using the dielectrophoretic crossover frequency and membrane breakdown voltage for each cell and evaluated the paired parameter efficiency concerning the identification of two different breast cancer cells and cell drug response. Moreover, we showed that the platform was able to identify cell electrical phenotyping, which was generated by subtle changes in cholesterol depletion-induced cell membrane integrity disruption when the paired parameter was used. Our platform introduced in this paper is extremely useful for facilitating more accurate and efficient evaluation of cell electrical phenotyping in a variety of applications, such as cell biology and drug discovery.

Recent advanced studies on flexible and stretchable electronic devices and optoelectronics have made possible a variety of soft and more functional electronic devices. With consumer demand for highly functional or free-form displays, high flexibility and stretchability in light-emitting devices are needed. Herein, we developed a unique structure of stretchable substrates with pillar arrays to reduce the stress on the active area of devices when strain is applied. We confirmed the advantages of the produced structures using mechanical simulation tools and determined that the structures effectively lessen the applied stress of interconnection as well as the active area in a stretched state. With this stress-relief stretchable substrate, we realized stretchable OLEDs that are compliant and maintain their performance under high strain deformation. Also, devices can be stretched in the biaxis, which is superior to only one-directional stretchable electronics; as such, devices can be used in practical applications like wearable electronics and health monitoring systems. We propose, for the first time, stretchable OLEDs patterned by the thermal evaporation fabrication process onto stress-relief substrates. These OLEDs can mitigate certain problems in previous studies of stretchable OLEDs without need to find new materials or to use a prestrained fabrication process.

Here, we report a new concept of both the adhesive manner and material, named "adhesive leaf (AL)," based on the leaf of the plant Heteropanax fragrans. The treatment of the corona discharge on the leaf surface can cause the nano-/microdestruction of the leaf epidermis, resulting in an outward release of sap. The glucose-containing sap provided the AL with a unique ability to stick to various substrates such as steel, polypropylene, and glass. Moreover, we reveal that the AL adhesion strength depends on the AL size, as well as the corona-discharge intensity. Conventional adhesives, such as glue and bond, lose their adhesive property and leave dirty residues upon the removal of the attached material. Unlike the conventional methods, the AL is advantageous as it can be repeatedly attached and detached thoroughly until the sap liquid is exhausted; its adhesive ability is maintained for at least three weeks at room temperature. Our findings shed light on a new concept of a biodegradable adhesive material that is created by a simple surface treatment.

Fiber-based wearable displays, one of the most desirable requisites of electronic textiles (e-textiles), have emerged as a technology for their capability to revolutionize textile and fashion industries in collaboration with the state-of-the-art electronics. Nonetheless, challenges remain for the fibertronic approaches, because fiber-based light-emitting devices suffer from much lower performance than those fabricated on planar substrates. Here, we report weavable and highly efficient fiber-based organic light-emitting diodes (fiber OLEDs) based on a simple, cost-effective and low-temperature solution process. The values obtained for the fiber OLEDs, including efficiency and lifetime, are similar to that of conventional glass-based counterparts, which means that these state-of-the-art, highly efficient solution processed planar OLEDs can be applied to cylindrical shaped fibers without a reduction in performance. The fiber OLEDs withstand tensile strain up to 4.3% at a radius of 3.5 mm and are verified to be weavable into textiles and knitted clothes by hand-weaving demonstrations. Furthermore, to ensure the scalability of the proposed scheme fiber OLEDs with several diameters of 300, 220, 120, and 90 μm, thinner than a human hair, are demonstrated successfully. We believe that this approach, suitable for cost-effective reel-to-reel production, can realize low-cost commercially feasible fiber-based wearable displays in the future.

In this study, a structurally and materially designed thin-film encapsulation is proposed to guarantee the reliability of transparent, flexible displays by significantly improving their barrier properties, mechanical stability, and environmental reliability, all of which are essential for organic light-emitting diode (OLED) encapsulation. We fabricated a bioinspired, nacre-like ZnO/Al 2 O 3 /MgO laminate structure (ZAM) using atomic layer deposition for the microcrack toughening effect. The ZAM film was formed with intentional voids and defects through the formation of a quasi-perfect sublayer, rather than the simple fabrication of nanolaminate structures. The 240 nm thick ZAM-based multibarrier (ZAM-TFE) with a compressively strained organic layer demonstrated an optical transmittance of 91.35% in the visible range, an extremely low water vapor transmission rate of 2.06 × 10 -6 g/m 2 /day, a mechanical stability enduring a strain close to 1%, and a residual stress close to 0, showing significant improvement of key TFE properties in comparison to an Al 2 O 3 -based multibarrier. In addition, ZAM-TFE demonstrated superior environmental resistance without degradation of barrier properties in a severe environment of 85 °C and 90% relative humidity (RH). Thus, our structurally and materially designed ZAM film has been well optimized in terms of its applicability as a gas diffusion barrier as well as in terms of its mechanical and environmental reliability. Finally, we confirmed the feasibility of the ZAM-TFE through application in OLEDs. The low-temperature ZAM-TFE technology showed great potential to provide a highly robust and flexible TFE of TFOLEDs.

In this study, a new and efficient dielectric-metal-dielectric-based thin-film encapsulation (DMD-TFE) with an inserted Ag thin film is proposed to guarantee the reliability of flexible displays by improving the barrier properties, mechanical flexibility, and heat dissipation, which are considered to be essential requirements for organic light-emitting diode (OLED) encapsulation. The DMD-TFE, which is composed of Al 2 O 3 , Ag, and a silica nanoparticle-embedded sol-gel hybrid nanocomposite, shows a water vapor transmission rate of 8.70 × 10 -6 g/m 2 /day and good mechanical reliability at a bending radius of 30 mm, corresponding to 0.41% strain for 1000 bending cycles. The electrical performance of a thin-film encapsulated phosphorescent organic light-emitting diode (PHOLED) was identical to that of a glass-lid encapsulated PHOLED. The operational lifetimes of the thin-film encapsulated and glass-lid encapsulated PHOLEDs are 832 and 754 h, respectively. After 80 days, the thin-film encapsulated PHOLED did not show performance degradation or dark spots on the cell image in a shelf-lifetime test. Finally, the difference in lifetime of the OLED devices in relation to the presence and thickness of a Ag film was analyzed by applying various TFE structures to fluorescent organic light-emitting diodes (FOLEDs) that could generate high amounts of heat. To demonstrate the difference in heat dissipation effect among the TFE structures, the saturated temperatures of the encapsulated FOLEDs were measured from the back side surface of the glass substrate, and were found to be 67.78, 65.12, 60.44, and 39.67 °C after all encapsulated FOLEDs were operated at an initial luminance of 10 000 cd/m 2 for sufficient heat generation. Furthermore, the operational lifetime tests of the encapsulated FOLED devices showed results that were consistent with the measurements of real-time temperature profiles taken with an infrared camera. A multifunctional hybrid thin-film encapsulation based on a dielectric-metal-dielectric structure was thus effectively designed considering the transmittance, gas-permeation barrier properties, flexibility, and heat dissipation effect by exploiting the advantages of each separate layer.

Recently, the role of clothing has evolved from merely body protection, maintaining the body temperature, and fashion, to advanced functions such as various types of information delivery, communication, and even augmented reality. With a wireless internet connection, the integration of circuits and sensors, and a portable power supply, clothes become a novel electronic device. Currently, the information display is the most intuitive interface using visualized communication methods and the simultaneous concurrent processing of inputs and outputs between a wearer and functional clothes. The important aspect in this case is to maintain the characteristic softness of the fabrics even when electronic devices are added to the flexible clothes. Silicone-based light-emitting diode (LED) jackets, shirts, and stage costumes have started to appear, but the intrinsic stiffness of inorganic semiconductors causes wearers to feel discomfort; thus, it is difficult to use such devices for everyday purposes. To address this problem, a method of fabricating a thin and flexible emitting fabric utilizing organic light-emitting diodes (OLEDs) was developed in this work. Its flexibility was evaluated, and an analysis of its mechanical bending characteristics and tests of its long-term reliability were carried out.

Understanding of the interactions of silver ions (Ag + ) with polynucleotides is important not only to detect Ag + over a wide range of concentrations in a simple, robust, and high-throughput manner but also to investigate the intermolecular interactions of hydrogen and coordinate interactions that are generated due to the interplay of Ag + , hydrogen ions (H + ), and polynucleotides since it is critical to prevent adverse environmental effects that may cause DNA damage and develop strategies to treat this damage. Here, we demonstrate a novel approach to simultaneously detect Ag + satisfying the above requirements and examine the combined intermolecular interactions of Ag + -polycytosine and H + -polycytosine DNA complexes using dielectrophoretic tweezers-based force spectroscopy. For this investigation, we detected Ag + over a range of concentrations (1 nM to 100 μM) by quantifying the rupture force of the combined interactions and examined the interplay between the three factors (Ag + , H + , and polycytosine) using the same assay for the detection of Ag + . Our study provides a new avenue not only for the detection of heavy metal ions but also for the investigation of heavy metal ions-polynucleotide DNA complexes using the same assay.

The direct quantification of weak intermolecular binding interactions is very important for many applications in biology and medicine. Techniques that can be used to investigate such interactions under a controlled environment, while varying different parameters such as loading rate, pulling direction, rupture event measurements, and the use of different functionalized probes, are still lacking. Herein, we demonstrate a biaxial dielectrophoresis force spectroscopy (BDFS) method that can be used to investigate weak unbinding events in a high-throughput manner under controlled environments and by varying the pulling direction (i.e., transverse and/or vertical axes) as well as the loading rate. With the BDFS system, we can quantitatively analyze binding interactions related to hydrogen bonding or ionic attractions between functionalized microbeads and a surface within a microfluidic device. Our BDFS system allowed for the characterization of the number of bonds involved in an interaction, bond affinity, kinetic rates, and energy barrier heights and widths from different regimes of the energy landscape.

Characterization of the stiffness of multiple particles trapped by tweezers-based force spectroscopy is a key step in building simple, high-throughput, and robust systems that can investigate the molecular interactions in a biological process, but the technology to characterize it in a given environment simultaneously is still lacking. We first characterized the stiffness of multiple particles trapped by dielectrophoretic (DEP) tweezers inside a microfluidic device. In this characterization, we developed a method to measure the thermal fluctuations of the trapped multiple particles with DEP tweezers by varying the heights of the particles in the given environment at the same time. Using the data measured in this controlled environment, we extracted the stiffness of the trapped particles and calculated their force. This study not only provides a simple and high-throughput method to measure the trap stiffness of multiple particles inside a microfluidic device using DEP tweezers but also inspires the application of the trapped multiple particles to investigate the dynamics in molecular interactions.

The random walk of spherical living cells on a silicon dioxide glassy substrate was studied experimentally and numerically. This random walk trajectory exhibited erratic dancing, which seemingly obeyed anomalous diffusion (i.e., Lévy-like walk) rather than normal diffusion. Moreover, the angular distribution (-π to π) of the cells' trajectory followed a "U-shaped pattern" in comparison to the uniform distribution seen in the movements of negatively charged polystyrene microspheres. These effects could be attributable to the homeostasis-driven structural resilient character of cells and physical interactions derived from temporarily retained nonspecific binding due to weak forces between the cells and substrates. Our results provide new insights into the stochastic behavior of mesoscopic biological particles with respect to structural properties and physical interactions.