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Recently, the application of cobalt iron boron (CoFeB) thin films in magnetic sensors has been widely studied owing to their high magnetic moment, anisotropy, and stability. However, most of these studies were conducted on rigid silicon substrates. For diverse applications of magnetic and angle sensors, it is important to explore the properties of ferromagnetic thin films grown on nonrigid deformable substrates. In this study, representative deformable substrates (polyimide (PI), polyethylene naphthalate (PEN), and polydimethylsiloxane (PDMS)), which can be bent or stretched, were used to assess the in-plane magnetic field angle-dependent properties of amorphous Ta/CoFeB/MgO/Ta thin films grown on deformable substrates. The effects of substrate roughness, tensile stress, deformable substrate characteristics, and sputtering on magnetic properties, such as the coercive field (Hc), remanence over saturation magnetization (Mr/Ms), and biaxial characteristics, were investigated. This study presents an unconventional foundation for exploring deformable magnetic sensors capable of detecting magnetic field angles.
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This paper investigates the submicron scale color filter design in the high-definition computer-generated hologram (HD-CGH). It is addressed that single pixel structural coloration is essential for full-color wide-viewing angle HD-CGH because the conventional RGB color stripe filter degrades HD-CGH image quality due to low misalignment tolerance. Considering that a submicron scale slit or hole with metallic mirror sidewalls can operate as a single pixel color filter. We propose a design of single pixel RGB plasmonic color filter (PCF) and present the feasibility of applying the proposed single pixel RGB PCF to high-definition HD-CGHs. Based on the RGB PCF platform, a 1.1 µm × 1.1 µm RGB PCF is designed and the corresponding optical characteristics of the full-color HD-CGH are analyzed.
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We report a mode-locked Alexandrite single pulse laser with cavity dumping. Mode locking was achieved by using an AOM and an EOM was used for Q-switching and cavity dumping. The instability of the single pulse laser energy output was reduced down to a tenth of that of the conventional single trigger system by introducing a novel double trigger system. The single pulse laser energy and pulse width were 100 mJ and 475 ps in multiple mode and 12.5 mJ and 275 ps in single mode, obtained without a laser amplifier.
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Signal enhancement of spectroscopies including terahertz time-domain spectroscopy (THz-TDS) and surface-enhanced Raman scattering (SERS) is a critical issue for effective molecular detection and identification. In this study, the sensing performance between THz-TDS and SERS individually accompanied by the proper plasmonic subwavelength structures was compared. For the precisely quantitative study on the optical properties of rhodamine 6G (R6G) dyes, SERS incorporates with the non-linearly enhanced Raman emissions at the molecular characteristic peaks while THz-TDS refers to the transmittance change and the shift of the spectral resonance. The local molecular density-dependent trade-off relationship between limit-of-detection and quenching was observed from both measurements. The specificity for two samples, R6G and methylene blue, is determined by the discriminations in spectral features such as the intensity ratio of assigned peaks in SERS and transmittance difference in THz-TDS. The comprehension of field enhancement by the specific nanostructures was supported by the finite-element method-based numerical computations. As a result, both spectroscopic techniques with the well-tailored nanostructures show great potential for highly sensitive, reproducible, label-free, and cost-effective diagnosis tools in the biomedical fields.
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Conventional sensors are rigid, involve complex processes and structures, and one sensor can detect only one type of stimulus. The manufacturing costs of such devices are high owing to the use of vacuum processes for the formation of thin films and electrodes and the complicated fabrication processes required to construct multiple layers. In addition, the multiple-layer design increases the risk of peeling due to mechanical movement. In this study, to solve the aforementioned problems, a simple two-layer multi-sensor has been fabricated using a non-vacuum solution process. The sensor consists of a light absorption layer comprising polyvinyl butyral and semiconductor particles and a top layer comprising two spiral-shaped Ag nanowire electrodes. The sensor experiences minimal damage by external adhesives and has a light-sensitive optical response at 420 nm and at 1.2 mW cm-2. Herein, the capacitance of the sensor applied to the two-electrode structure was determined, along with the light sensitivity and change in noise with frequency. We believe that the proposed multi-sensor can be applied in a wide range of fields because it can act as a touch sensor and light sensor.
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Coaxial type piezoelectric energy generator (C-PEG) nanofiber was fabricated by a self-designed continuous electrospinning deposition system. Piezoelectric PVDF-TrFE nanofiber as an electroactive material was electrospun at a discharge voltage of 9-12 kV onto a simultaneously rotating and transverse moving Cu metal wire at an angular velocity of ω g = 60-120 RPM. The piezoelectric coefficient d33 of the PVDF-TrFE nanofiber was approximately -20 pm V-1. The generated output voltage (V G) increased according to the relationship exp(-α P) (α = 0.41- 0.57) as the pressure (P) increased from 30 to 500 kpa. The V G values for ten and twenty pieces of C-PEG were V G = 3.9 V and 9.5 V at P = 100 kpa, respectively, relatively high output voltages compared to previously reported values. The high V G for the C-PEG stems from the fact that it can generate a fairly high V G due to the increased number of voltage collection points compared to a conventional two-dimensional (2-dim) capacitor type of piezoelectric film or fiber device. C-PEG yarn was also fabricated via the dip-coating of a PDMS polymer solution, followed by winding with Ag-coated nylon fiber as an outer electrode. The current and power density of ten pieces of C-PEG yarn were correspondingly 22 nA cm-2 and 8.6 µW cm-3 at V G = 1.97 V, higher than previously reported values of 5.54 and 6 µW cm-3. The C-PEG yarn, which can generate high voltage compared to the conventional film/nanofiber mat type, is expected to be very useful as a wearable energy generator system.
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In this study, random nanoscale rods (RNRs) with a double refractive index were fabricated via spin coating, dry etching, and sputtering, which are processes that are extensively applied in industry. With regard to optical properties, the RNRs with a double refractive index (RNRsD) exhibited a total transmittance that was >90% in the visible range and an optical haze in the range of 42%-50% at a wavelength of 520 nm. Organic light-emitting diodes (OLEDs) with RNRsD, where SiO2 was deposited on the RNRs via radiofrequency sputtering, exhibited an enhancement of 34.5% in the external quantum efficiency compared with OLEDs with the bare substrate. Furthermore, the color variation of the OLEDs with the optimal RNRsD with respect to a change in the viewing angle was improved from color coordinates of Δ(x, y) = (0.032, 0.034) to Δ(x, y) = (0.014, 0.014). Therefore, the proposed film can be used as a scattering layer for enhancing the light extraction and viewing angle of OLEDs by reducing the substrate mode light loss and changing the direction of light. In addition to using a low-temperature fabrication process that does not employ a photomask and a lithographic template, the proposed method is applicable to flexible devices because it uses a polymer and a thin inorganic film.
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Light extraction in organic light-emitting diodes (OLEDs) was improved by applying SnO x nanocones grown via thermal annealing in a low-O2 atmosphere. SnO x was easily fabricated through thermal processing after Sn deposition. The diameter of the SnO x nanocones was controlled by changing the deposition thickness of Sn. The SnO x nanocones induced strong Mie scattering, which reduced the total internal reflection in the glass substrate. Consequently, the OLED with SnO x nanocones exhibited a 23% increase in the external quantum efficiency compared with a reference device.
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This paper presents a wearable hand module which was made of five fiber Bragg grating (FBG) strain sensor and algorithms to achieve high accuracy even when worn on different hand sizes of users. For real-time calculation with high accuracy, FBG strain sensors move continuously according to the size of the hand and the bending of the joint. Representatively, four algorithms were proposed; point strain (PTS), area summation (AREA), proportional summation (PS), and PS/interference (PS/I or PS/I_α). For more accurate and efficient assessments, 3D printed hand replica with different finger sizes was adopted and quantitative evaluations were performed for index~little fingers (77 to 117 mm) and thumb (68~78 mm). For index~little fingers, the optimized algorithms were PS and PS/I_α. For thumb, the optimized algorithms were PS/I_α and AREA. The average error angle of the wearable hand module was observed to be 0.47 ± 2.51° and mean absolute error (MAE) was achieved at 1.63 ± 1.97°. These results showed that more accurate hand modules than other glove modules applied to different hand sizes can be manufactured using FBG strain sensors which move continuously and algorithms for tracking this movable FBG sensors.
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Técnicas Biosensibles , Dedos/anatomía & histología , Mano/anatomía & histología , Dispositivos Electrónicos Vestibles , Algoritmos , Humanos , Impresión TridimensionalRESUMEN
With ever-growing technological demands in the imaging sensor industry for autonomous driving and augmented reality, developing sensors that can satisfy not only image resolution but also the response speed becomes more challenging. Herein, the focus is on developing a high-speed photosensor capable of obtaining high-resolution, high-speed imaging with colloidal quantum dots (QDs) as the photosensitive material. In detail, high-speed QD photodiodes are demonstrated with rising and falling times of τr = 28.8 ± 8.34 ns and τf = 40 ± 9.81 ns, respectively, realized by fast separation of electron-hole pairs due to the action of internal electric field at the QD interface, mainly by the interaction between metal oxide and the QD's ligands. Such energy transfer relations are analyzed and interpreted with time-resolved photoluminescence measurements, providing physical understanding of the device and working principles.
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The development of high performance gas sensors that operate at room temperature has attracted considerable attention. Unfortunately, the conventional mechanism of chemiresistive sensors is restricted at room temperature by insufficient reaction energy with target molecules. Herein, novel strategy for room temperature gas sensors is reported using an ionic-activated sensing mechanism. The investigation reveals that a hydroxide layer is developed by the applied voltages on the SnO2 surface in the presence of humidity, leading to increased electrical conductivity. Surprisingly, the experimental results indicate ideal sensing behavior at room temperature for NO2 detection with sub-parts-per-trillion (132.3 ppt) detection and fast recovery (25.7 s) to 5 ppm NO2 under humid conditions. The ionic-activated sensing mechanism is proposed as a cascade process involving the formation of ionic conduction, reaction with a target gas, and demonstrates the novelty of the approach. It is believed that the results presented will open new pathways as a promising method for room temperature gas sensors.
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We investigate spectral responses of two different terahertz (THz) metamaterials of double split ring resonator (DSRR) and the nano slot resonator (NSR) for molecule sensing in low concentration. Two different resonant frequencies of DSRR can be controlled by polarization angle of incident THz beam. For comparison of THz optical characteristics, two NSRs were made as showing the same resonant frequencies as DSRR's multimode. The monosaccharide molecules of glucose and galactose were detected by these two types of metamaterials matching the resonant frequencies in various concentration. NSR shows higher sensitivity in very low concentration range rather than DSRR, although the behavior was easily saturated in terms of concentration. In contrast, DSRR can cover more broad concentration range with clear linearity especially under high quality factor mode in polarization of 67.5 degree due to the Fano resonance. THz field enhancement distributions were calculated to investigate sensing performance of both sensing chips in qualitative and quantitative manner.
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One of the main challenges in the widespread utilization of localized plasmon resonance-based biosensors is the fabrication of large-area and low-cost plasmonic nanostructures. In this work, we fabricated large-area and low-cost complementary plasmonic biosensors such as nanohole and nanodisk arrays using dual nanotransfer printing (NTP) with a single metal deposition and a single reusable mold. The suspended nanohole arrays and the suspended nanodisk arrays were fabricated using the subsequent dry etching process. We confirmed a maximum enhancement in bulk sensitivity in experiments and simulations by controlling the vertical and lateral etching depths of the dielectric layer underneath the gold (Au) nanohole and nanodisk arrays. Furthermore, we show that the surface sensitivity evaluated by atomic layer deposition of aluminum oxide increased because appropriate vertical and lateral etching depths allow the target analyte to access the additional near-field formed at the bottom of the Au nanostructure. The dual NTP method provides a practical solution for the realization of large-area and low-cost label-free plasmonic biosensing systems, with a reduction in complexity and cost of the fabrication process of complementary plasmonic structures and metasurfaces.
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Técnicas Biosensibles/instrumentación , Impresión Tridimensional/instrumentación , Análisis por Micromatrices , Resonancia por Plasmón de Superficie , Propiedades de SuperficieRESUMEN
Organic light-emitting diodes with a quasi-periodic nano-structure (QPS) were fabricated via a combination of laser interference lithography (LIL) and reactive ion etching (RIE). The LIL process was used to generate a periodic pattern, whereas the RIE process was used as a supplement to add randomness to the periodic pattern. The period of the fabricated periodic pattern was determined by finite difference time domain solutions. The height and density of the QPS were controlled by the RIE etching time and were optimized. The resulting quasi-periodic nanostructure comprised silicon dioxide (SiO2) with a low refractive index (n = 1.4-1.5), and an external quantum efficiency enhancement of 18% was achieved using the QPS device, without any viewing angle problems or spectral distortion, which are serious drawbacks of periodic patterns.
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Herein, we introduce an interdigitated horizontal electrode (IHE) structure with a metal-based electron-collecting (or -injecting) electrode and a hole-collecting (or -injecting) electrode composed of a conductive polymeric material that has a nanoscale distance and is horizontally separated. In the IHE, a metal electrode is fabricated on a silicon-oxide substrate, and a self-assembled monolayer (SAM) is selectively bonded to the metal and the oxide to form a conductive polymer electrode by dip coating. Each of the SAM materials is composed of a head part bonded to the substrate surface and a tail part that is hydrophilic or hydrophobic. This inherent property makes the metal electrode hydrophobic and the oxide substrate hydrophilic. Ag is used as a metal electrode material and is combined with alkanethiol SAMs. The alkylsilane SAMs are combined with the silicon oxide substrate to make them hydrophilic, using poly (3, 4-ethylenedioxythiophene)-poly (PEDOT: PSS) as the conductive polymer material. In this study, we have found that there is a difference in the spacing between the two electrodes that depends on the combination of SAM materials. Each interval was spaced from a minimum of 140 nm to a maximum of 385 nm.
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In this study, we fabricate solution processable, flexible, and transparent hybrid electrodes. The hybrid electrodes are designed by depositing a tungsten trioxide (WO3) buffer layer on silver nanowires. The fabrication method is solution based, and the electrodes can be fabricated directly on a flexible substrate at low temperatures. This fabrication method is cost-effective and scalable. The hybrid electrodes show high flexibility, transparency, and conductivity. In addition, since the thickness of the WO3 buffer layer can be controlled, the transparency, conductivity, and surface roughness of the hybrid electrodes can be tailored. These hybrid electrodes are potential alternatives to conventional indium tin oxide electrodes for flexible electronic devices.
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Carbon black and titanium dioxide have been widely used as pigment particles for electrophoretic displays. However, the effect of external water vapor on these pigment particles has not yet been presented. Therefore, in this work, we report the clumping phenomenon between pigment particles as a result of water vapor absorption. To verify clumping between pigment particles, various analysis techniques were used, including scanning electron microscopy, atomic force microscopy, zeta potential measurement, and Raman spectroscopy. We examined the Raman spectrum of carbon black to demonstrate the effect of water vapor absorption on particles. According to the Raman spectrum analysis, the 2D and 2D' peak intensities were significantly increased; moreover, the full widths at half maximum were modified. Thus, we concluded that water vapor absorption on pigment particles can induce the clumping phenomenon on pigments. To protect an electrophoretic display device from external gas transmission, we applied a nanocomposites gas barrier film to the device. The device lifetime was consequently improved by 336%.
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We propose a method to improve the axial response of structured illumination microscopy via selection of an illumination pattern with a sinusoidal or square wave within the cutoff frequency of the imaging system. Residual modulation within a sectioned image is mitigated by accurate phase-shifting via the electrical spatial light modulator control signal, which is based on an illumination pattern having a suitable waveform. Reduction in residual modulation is observed in the sinusoidal pattern with a spatial frequency sufficiently below the cutoff frequency of the imaging system. This reduction is larger for the square wave as the spatial frequency approaches one-third of the cutoff frequency.
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Fabrication of junction-free Ag fiber electrodes for flexible organic light-emitting diodes (OLEDs) is demonstrated. The junction-free Ag fiber electrodes are fabricated by electrospun polymer fibers used as an etch mask and wet etching of Ag thin film. This process facilitates surface roughness control, which is important in transparent electrodes based on metal wires to prevent electrical instability of the OLEDs. The transmittance and resistance of Ag fiber electrodes can be independently adjusted by controlling spinning time and Ag deposition thickness. The Ag fiber electrode shows a transmittance of 91.8% (at 550 nm) at a sheet resistance of 22.3 Ω â¡-1 , leading to the highest OLED efficiency. In addition, Ag fiber electrodes exhibit excellent mechanical durability, as shown by measuring the change in resistance under repeatable mechanical bending and various bending radii. The OLEDs with Ag fiber electrodes on a flexible substrate are successfully fabricated, and the OLEDs show an enhancement of EQE (≈19%) compared to commercial indium tin oxide electrodes.
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In this research, we developed a wearable temperature-sensing element by dip dyeing threads in poly (3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) (p-type conducting polymer) solution. The PEDOT:PSS was used to dye the textile and it exhibited negative temperature coefficient characteristics in which the resistance decreases as the temperature increases. The fabricated temperature-detection thread achieved a sensitivity of 167.1 Ω/°C with 99.8% linearity in the temperature range of -50 °C to 80 °C. We anticipate that temperature sensors that apply our technology will be made as stitch- or textile-type for wearable devices, and they will be widely adopted for different applications such as in fitness, leisure, healthcare, medical treatment, infotainment, industry, and military applications, among others.