Designing Novel LiDAR-Detectable Plate-Type Materials: Synthesis, Chemistry, and Practical Application for Autonomous Working Environment.

Plate-type hollow black TiO2 (HL/BT) with a high NIR reflectance was fabricated for the first time as a LiDAR-detectable black material. A TiO2 layer was formed on commercial-grade glass by using the sol-gel method to obtain a plate-type structure. The glass template was then etched with hydrofluoric acid to form a hollow structure, and blackness was further achieved through NaBH4 reduction, which altered the oxidation state of TiO2 to black TixO2x-1 or Ti4+ to Ti3+ and Ti2+. The blackness of the HL/BT material was maintained by a novel approach that involved etching prior to reduction. The thickness of the TiO2 layer was controlled to maximize the NIR reflectance when applied as paint. The HL/BT material with a thickness of 140 nm (HL/BT140) showed a blackness (L*) of 13.3 and high NIR reflectance of 23.6% at a wavelength of 905 nm. This is attributed to the effective light reflection at the interface created by the TiO2 layer and the hollow structure. Plate-type HL/BT140 provides excellent spreadability, durability, and thermal stability in practical paint applications compared with sphere-type materials due to the higher contacting area to the applied surface, making it suitable for use as a LiDAR-detectable inorganic black pigment in autonomous environments.

Designing a highly near infrared-reflective black nanoparticles for autonomous driving based on the refractive index and principle.

HYPOTHESIS: The development of highly NIR reflective black single-shell hollow nanoparticles (BSS-HNPs) can overcome the Light Detection and Ranging (LiDAR) sensor limitations of dark-tone materials. The crystalline phase of TiO2 and the refractive index can be controlled by calcination temperature. The formation of hollow structure and the refractive index is expected to simultaneously increase the light reflection and LiDAR detectability. EXPERIMENTS: The BSS-HNPs are synthesized using the sol-gel method, calcination, NaBH4 reduction, and etching to form a hollow structure with true blackness. The computational bandgap calculation is conducted to determine the bandgap energy (Eg) of the white and black TiO2 with different crystalline structures. The blackness of the as-synthesized materials is determined by the Commission on Illumination (CIE) L*a*b* color system. FINDINGS: The hydrophilic nature of BSS-HNPs enables the formulation of hydrophilic paints, allowing the mono-layer coating. With the synergistic effects of hollow structure and the refractive index, BSS-HNPs manifested superb NIR reflectance at LiDAR detection wavelengths. The high detectability, blackness, and hollow structure of BSS-HNPs can expand the variety of LiDAR-detectable dark-tone materials.

Vivid-Colored Electrorheological fluids with simultaneous enhancements in color clarity and Electro-Responsivity.

HYPOTHESIS: Surface modification of dielectric materials changes the dipole-dipole interactions under electric fields, thereby controlling the electrorheological (ER) response. The introduction of metal oxides onto mica templates and further coating of dyes is expected to simultaneously improve the color clarity and ER performance. EXPERIMENTS: Dye-coated TiO2 platelets on mica are synthesized for high-performance colorful ER fluids. A sol-gel method is utilized to grow TiO2 on mica to prepare precursor light-colored mica/TiO2 materials, which are coated with appropriate dyes to enhance the vividness as determined by the Commission Internationale de clairage L*a*b* color system. The color expression and color clarity improvement are explained via the light interference effect and the presence of chromophores. FINDINGS: The uniform TiO2 layers can be obtained under low pH conditions with controlled nucleation kinetics. The addition of dyes to TiO2 increases the surface area and porosity of ER materials and introduces heteroatoms that act as positive factors. In practical ER applications, dye-coated TiO2-based ER fluids exhibit higher ER performances compared with the corresponding light-colored TiO2-based ER fluids. The vivid-colored ER fluids could provide an easy selection for a wide range of rheological systems requiring a specific magnitude of stress by confirming the color.

A Study on Enhanced Electrorheological Performance of Plate-like Materials via Percolation Gel-like Effect.

The use of plate-like materials to induce a percolation gel-like effect in electrorheological (ER) fluids is sparsely documented. Hence, we dispersed plate-like materials, namely natural mica, synthetic mica, and glass, as well as their pulverized particles, in various concentrations in silicone oil to form ER fluids. Subsequently, the rheological properties of the fluids were evaluated and compared to identify the threshold concentration for percolating a gel-like state. The shear stress and viscoelastic moduli under zero-field conditions confirmed that plate-like materials can be used to induce percolation gel-like effects in ER fluids. This is because of the high aspect ratio of the materials, which enhances their physical stability. In practical ER investigations, ER fluids based on synthetic mica (30.0 wt%) showed the highest yield stress of 516.2 Pa under an electric field strength of 3.0 kV mm-1. This was attributed to the formation of large-cluster networks and additional polarization induced by the ions. This study provides a practical approach for developing a new type of gel-like ER fluid.

Preparation of a High-Performance Asymmetric Supercapacitor by Recycling Aluminum Paper and Filter Components of Heated Tobacco.

In this study, Al paper and cellulose acetate (CA) filters derived from heated tobacco waste were successfully converted into current collectors and active materials for a supercapacitor device. Typically, heated tobacco contains electrically discontinuous Al paper. First, Al was extracted from the tobacco waste using HCl to produce Lewis acid (AlCl3). This acid was then used in an Al electrodeposition process utilizing the chloroaluminate ionic liquid reaction between the acid and the base (RCl) at room temperature. To enhance the conductivity, a supplementary coating of Al metal was applied to the Al paper through electrodeposition, thus re-establishing the electrical continuity of the discontinuous parts and forming an Al-coated current collector. Moreover, the CA filters were carbonized under a nitrogen atmosphere, yielding carbon precursors (C-CA) for the supercapacitor electrodes. To further enhance the electrochemical performance, nickel oxide (NiO) was incorporated into C-CA, resulting in C-CA@NiO with pseudocapacitance. The specific surface area of CA increased with carbonization and the subsequent incorporation of NiO. The as-synthesized C-CA and C-CA@NiO materials were applied to an Al-coated current collector to obtain C-CA- and C-CA@NiO-based electrodes, exhibiting stable electrochemical behavior in the voltage range of -1.0 to 0 V and 0 to 1.0 V, respectively. An asymmetric supercapacitor (ASC) device was assembled with C-CA@NiO and C-CA as the positive and negative electrodes, respectively. This ASC device demonstrated a high specific capacitance of 40.8 F g-1, while widening the operating voltage window to 2.0 V. The high electrochemical performance of the device is attributed to the successful Al electrodeposition, which facilitates the electrical conductivity and increased porosity of the C-CA@NiO and C-CA materials. To the best of our knowledge, this is a pioneering study in regards to the conversion of biomass waste into current collectors and active materials to fabricate a practical ASC device. Our findings highlight the potential of reusing Al paper and CA filters from heated tobacco waste as essential components of energy storage devices.

A novel of WS2-MoCuO3 supported with graphene quantum dot as counter electrode for dye-sensitized solar cells application.

A novel tungsten disulfide-molybdenum copper oxide composite supported with graphene quantum dots (WM@GQDs) has been synthesized as a counter electrode (CE) for dye-sensitized solar cells (DSSCs) using a simple and low-cost ultrasonication method. The unique structure of WM@GQDs exhibits excellent power conversion efficiency due to its high catalytic activity and charge transport properties. In addition, the graphene quantum dots (GQDs) provide more active sites in the zero-dimensional materials for an I/I3- redox reaction which can improve the electrical and optical properties of the composite. The results indicate that the amount of GQDs in the composite affect the effectiveness of solar devices. When 0.9%wt of GQDs was used, the WM@GQDs composite achieved an efficiency of 10.38%, which is higher than that of the expensive platinum CE under the same conditions. The mechanism behind the improved power conversion efficiency (PCE) of the composite sample is also discussed in detail. Therefore, WM@GQDs can be an efficient material to replace platinum in DSSCs as a CE.

3D Hierarchically Structured Tin Oxide and Iron Oxide-Embedded Carbon Nanofiber with Outermost Polypyrrole Layer for High-Performance Asymmetric Supercapacitor.

Herein, unique three-dimensional (3D) hierarchically structured carbon nanofiber (CNF)/metal oxide/conducting polymer composite materials were successfully synthesized by combinations of various experimental methods. Firstly, base CNFs were synthesized by carbonization of electrospun PAN/PVP fibers to attain electric double-layer capacitor (EDLC) characteristics. To further enhance the capacitance, tin oxide (SnO2) and iron oxide (Fe2O3) were coated onto the CNFs via facile hydrothermal treatment. Finally, polypyrrole (PPy) was introduced as the outermost layer by a dispersion polymerization method under static condition to obtain 3D-structured CNF/SnO2/PPy and CNF/Fe2O3/PPy materials. With each synthesis step, the morphology and dimension of materials were transformed, which also added the benign characteristic for supercapacitor application. For the practical application, as-synthesized CNF/SnO2/PPy and CNF/Fe2O3/PPy were applied as active materials for supercapacitor electrodes, and superb specific capacitances of 508.1 and 426.8 F g-1 (at 1 A g-1) were obtained (three-electrode system). Furthermore, an asymmetric supercapacitor (ASC) device was assembled using CNF/SnO2/PPy as the positive electrode and CNF/Fe2O3/PPy as the negative electrode. The resulting CNF/SnO2/PPy//CNF/Fe2O3/PPy device exhibited excellent specific capacitance of 101.2 F g-1 (at 1 A g-1). Notably, the ASC device displayed a long-term cyclability (at 2000 cycles) with a retention rate of 81.1%, compared to a CNF/SnO2//CNF/Fe2O3 device of 70.3% without an outermost PPy layer. By introducing the outermost PPy layer, metal oxide detachment from CNFs were prevented to facilitate long-term cyclability of electrodes. Accordingly, this study provides an effective method for manufacturing a high-performance and stable supercapacitor by utilizing unique 3D hierarchical materials, comprised of CNF, metal oxide, and conducting polymer.

Fluorophores-rich natural powder from selected medicinal plants for detection latent fingerprints and cyanide.

Forensic science is currently fast-growing for the development detection of the latent fingerprint. Currently, chemical dust quickly enters the body through touch or inhalation and will be affected by the user. In this research, a study on the comparison of natural powder from four species of medicinal plants (Zingiber montanum, Solanum Indicum L., Rhinacanthus nasutus, and Euphorbia tirucall) for the detection of latent fingerprints is carried out that has fewer adverse effects on the user's body by using such natural substances instead. In addition, the fluorescence properties of the dust have been found in some natural powder for sample detection and appear on multi-colored surfaces to show that the latent fingerprints are more pronounced than ordinary dust. In this study, medicinal plants have also been applied to detect cyanide, as it has been known that it is hazardous for humans and can be used as a poisonous compound to kill someone. The characteristics of each powder have also been analyzed using naked-eye detection under UV light, Fluorescence spectrophotometer, FIB-SEM, and FTIR. All the powder obtained can then be used for high potential detection of latent fingerprints on the non-porous surface with their specific characteristics and trace amounts of cyanide using turn-on-off fluorescent sensing method.

Controlled Growth of Semiconducting ZnO Nanorods for Piezoelectric Energy Harvesting-Based Nanogenerators.

Zinc oxide (ZnO) nanorods have attracted considerable attention in recent years owing to their piezoelectric properties and potential applications in energy harvesting, sensing, and nanogenerators. Piezoelectric energy harvesting-based nanogenerators have emerged as promising new devices capable of converting mechanical energy into electric energy via nanoscale characterizations such as piezoresponse force microscopy (PFM). This technique was used to study the piezoresponse generated when an electric field was applied to the nanorods using a PFM probe. However, this work focuses on intensive studies that have been reported on the synthesis of ZnO nanostructures with controlled morphologies and their subsequent influence on piezoelectric nanogenerators. It is important to note that the diatomic nature of zinc oxide as a potential solid semiconductor and its electromechanical influence are the two main phenomena that drive the mechanism of any piezoelectric device. The results of our findings confirm that the performance of piezoelectric devices can be significantly improved by controlling the morphology and initial growth conditions of ZnO nanorods, particularly in terms of the magnitude of the piezoelectric coefficient factor (d33). Moreover, from this review, a proposed facile synthesis of ZnO nanorods, suitably produced to improve coupling and switchable polarization in piezoelectric devices, has been reported.

Recent Advances in Two-Dimensional MXene for Supercapacitor Applications: Progress, Challenges, and Perspectives.

MXene is a type of two-dimensional (2D) transition metal carbide and nitride, and its promising energy storage materials highlight its characteristics of high density, high metal-like conductivity, tunable terminals, and charge storage mechanisms known as pseudo-alternative capacitance. MXenes are a class of 2D materials synthesized by chemical etching of the A element in MAX phases. Since they were first discovered more than 10 years ago, the number of distinct MXenes has grown substantially to include numerous MnXn-1 (n = 1, 2, 3, 4, or 5), solid solutions (ordered and disordered), and vacancy solids. To date, MXenes used in energy storage system applications have been broadly synthesized, and this paper summarizes the current developments, successes, and challenges of using MXenes in supercapacitors. This paper also reports the synthesis approaches, various compositional issues, material and electrode topology, chemistry, and hybridization of MXene with other active materials. The present study also summarizes MXene's electrochemical properties, applicability in pliant-structured electrodes, and energy storage capabilities when using aqueous/non-aqueous electrolytes. Finally, we conclude by discussing how to reshape the face of the latest MXene and what to consider when designing the next generation of MXene-based capacitors and supercapacitors.

Fabrication of Flexible All-Solid-State Asymmetric Supercapacitor Device via Full Recycling of Heated Tobacco Waste Assisted by PLA Gelation Template Method.

In this study, a flexible all-solid-state asymmetric supercapacitor (FASC) device has been successfully fabricated via full recycling of heated tobacco waste (HTW). Tobacco leaves and cellulose acetate tubes have been successfully carbonized (HTW-C) and mixed with metal oxides (MnO2 and Fe3O4) to obtain highly active materials for supercapacitors. Moreover, poly(lactic acid) (PLA) filters have been successfully dissolved in an organic solvent and mixed with the as-prepared active materials using a simple paste mixing method. In addition, flexible MnO2- and Fe3O4-mixed HTW-C/PLA electrodes (C-MnO2/PLA and C-Fe3O4/PLA) have been successfully fabricated using the drop-casting method. The as-synthesized flexible C-MnO2/PLA and C-Fe3O4/PLA electrodes have exhibited excellent electrical conductivity of 378 and 660 µS cm-1, and high specific capacitance of 34.8 and 47.9 mF cm-2 at 1 mA cm-2, respectively. A practical FASC device (C-MnO2/PLA//C-Fe3O4/PLA) has been assembled by employing the C-MnO2/PLA as the positive electrode and C-Fe3O4/PLA as the negative electrode. The as-prepared FASC device showed a remarkable capacitance of 5.80 mF cm-2 at 1 mA cm-2. Additionally, the FASC device manifests stable electrochemical performance under harsh bending conditions, verifying the superb flexibility and sustainability of the device. To the best of our knowledge, this is the first study to report complete recycling of heated tobacco waste to prepare the practical FASC devices. With excellent electrochemical performance, the experiments described in this study successfully demonstrate the possibility of recycling new types of biomass in the future.

Recent Progress on Functionalized Graphene Quantum Dots and Their Nanocomposites for Enhanced Gas Sensing Applications.

Gas-sensing technology has witnessed significant advancements that have been driven by the emergence of graphene quantum dots (GQDs) and their tailored nanocomposites. This comprehensive review surveys the recent progress made in the construction methods and applications of functionalized GQDs and GQD-based nanocomposites for gas sensing. The gas-sensing mechanisms, based on the Fermi-level control and charge carrier depletion layer theory, are briefly explained through the formation of heterojunctions and the adsorption/desorption principle. Furthermore, this review explores the enhancements achieved through the incorporation of GQDs into nanocomposites with diverse matrices, including polymers, metal oxides, and 2D materials. We also provide an overview of the key progress in various hazardous gas sensing applications using functionalized GQDs and GQD-based nanocomposites, focusing on key detection parameters such as sensitivity, selectivity, stability, response and recovery time, repeatability, and limit of detection (LOD). According to the most recent data, the normally reported values for the LOD of various toxic gases using GQD-based sensors are in the range of 1-10 ppm. Remarkably, some GQD-based sensors exhibit extremely low detection limits, such as N-GQDs/SnO2 (0.01 ppb for formaldehyde) and GQD@SnO2 (0.10 ppb for NO2). This review provides an up-to-date perspective on the evolving landscape of functionalized GQDs and their nanocomposites as pivotal components in the development of advanced gas sensors.

A flexible mesoporous Cu doped FeSn-G-SiO2 composite based biosensor for microalbumin detection.

A new mesoporous Cu-doped FeSn-G-SiO2 (CFSGS) based biosensor was developed for the detection of microalbumin in urine samples. The mechanically flexible FeSn modified sensor was fabricated at room temperature. These demonstrations highlight the unexplored potential of FeSn for developing novel biosensing devices. It is extremely sensitive and selective. Surfactant-aided self-assembly was used to synthesise the mesoporous CFSGS. The large surface area due to the mesopore presence in the CFSG surface that has been composited inside the mesoporous SiO2 boosted the electrochemical detection. The linear range and detection limit of microalbumin under optimum circumstances were 0.42 and 1 to 10 µL, respectively. This easily fabricated mesoporous CFSGS provided a fast response with high sensitivity, and good selectivity. The sensor's reusability and repeatability were also quite high, with just a 90 percent drop after 4 weeks of storage at ambient temperature. The biosensor also demonstrated high selectivity against typical potential interfering chemicals found in urine (ascorbic acid, urea, and sodium chloride). The good performance of the mesoporous CFSGS biosensor was validated by measuring microalbumin, and the findings indicated that this sensing device performed very well.

Improving Minutiae Image of Latent Fingerprint Detection on Non-Porous Surface Materials under UV Light Using Sulfur Doped Carbon Quantum Dots from Magnolia Grandiflora Flower.

In this study, carbon quantum dots (CQDs) from Magnolia Grandiflora flower as a carbon precursor were obtained using a hydrothermal method under the optimized conditions affected by various heating times (14, 16, 18, and 20 min) and various electric power inputs (900-1400 W). Then, hydrogen sulfide (H2S) was added to dope the CQDs under the same manner. The aqueous solution of the S-CQDs were characterized by FTIR, XPS, EDX/SEM, and TEM, with nanoparticle size at around 4 nm. Then, the as-prepared S-CQDs were successfully applied with fine corn starch for detection of minutiae latent fingerprints on non-porous surface materials. It is demonstrated that the minutiae pattern is more clearly seen under commercial UV lamps with a bright blue fluorescence intensity. Therefore, this research has proved that the S-CQDs derived from plant material have a better potential as fluorescent probes for latent fingerprint detection.

Hollow TiO2 Nanoparticles Capped with Polarizability-Tunable Conducting Polymers for Improved Electrorheological Activity.

Hollow TiO2 nanoparticles (HNPs) capped with conducting polymers, such as polythiophene (PT), polypyrrole (PPy), and polyaniline (PANI), have been studied to be used as polarizability-tunable electrorheological (ER) fluids. The hollow shape of TiO2 nanoparticles, achieved by the removal of the SiO2 template, offers colloidal dispersion stability in silicone oil owing to the high number density. Conducting polymer shells, introduced on the nanoparticle surface using vapor deposition polymerization method, improve the yield stress of the corresponding ER fluids in the order of PANI < PPy < PT. PT-HNPs exhibited the highest yield stress of ca. 94.2 Pa, which is 5.0-, 1.5-, and 9.6-times higher than that of PANI-, PPy-, and bare HNPs, respectively. The improved ER response upon tuning with polymer shells is attributed to the space charge contribution arising from the movement of the charge carriers trapped by the heterogeneous interface. The ER response of studied ER fluids is consistent with the corresponding polarizability results as indicated by the permittivity and electrophoretic mobility measurements. In conclusion, the synergistic effect of hollow nanostructures and conducting polymer capping effectively enhanced the ER performance.

Effect of Extremely Short-Sized MWCNT as Additive Material in High Surface Area Activated Carbon and Its Enhanced Electrical LIC Performance.

Extremely short-sized multi-wall carbon nanotube (CNT) and high surface area activated carbon were used to increase the electrical performance of lithium-ion capacitors (LIC). After electrodes were synthesized using extremely short-sized CNTs and high specific surface area activated carbon, their electrochemical characteristics were evaluated by XRD, SEM, TEM, cyclic voltammetry, EIS, BET, adoption isotherm, t-plot, and pore size distribution. In the process of electrode preparation using extremely short-sized CNTs and high specific surface area activated carbon, CNTs certainly caused a space-filling effect between these two materials, which had a significant effect on the evaluation of electrical characteristics. These relationships were demonstrated by the results of adsorption-desorption isotherm, pore size distribution, t-plot, and BJH plot. Particularly, in the electrochemical cyclic test, as the content of CNT increased, the current density significantly increased with the formation of a near-perfect rectangular shape. This tendency also exhibited excellent characteristics in a t-I plot, Tafel plot, and LSV plot, which clearly affected the electrochemical oxidation-reduction reaction due to the densification of filling density and space structure by adding extremely short-sized CNTs to the active material. In addition, YP80_CNT3 formed a specific resistance value in the range of 7.2 to 6.2 Ω/cm2, showing significantly reduced values compared to other samples. This research presented herein offers a promising route for the rational design of MWCNT and stable electrochemical reaction with LIC working mechanism.

Novel Approach to Synthesis of AgZnS and TiO2 Decorated on Reduced Graphene Oxide Ternary Nanocomposite for Hydrogen Evolution Effect of Enhanced Synergetic Factors.

In this work, a novel ternary nanocomposites AgZnS-TiO2-reduced graphene oxide (RGO) was successfully synthesized by a facile soft ultrasonic-reduction condition as low as 70 °C. During the ultrasound reaction, the reduction of GO and the growth of AgZnS and TiO2 crystals occurred simultaneously in conjunction with the deposition of AgZnS and TiO2 crystals onto the surface of the graphene. The synthesized nanocatalysts were characterized by XRD, SEM, TEM, EDX, Raman spectroscopy, XPS, UV-Vis DRS, photoluminescence spectrometer, and photocurrent and CV. The AgZnS-G-T was shown as catalytic HER with some synnegetic factors such as pH-universal, temperature, and ultrasonic condition. After 4 h, it was observed that AgZnS-TiO2-RGO has the highest efficiency of photocatalytic activity through hydrogen production by water splitting, which achieved the highest hydrogen evolution rate of 930.45 µmol/g at buffer solution (pH = 5), which was superior to AgZnS-G (790.1 µmole/g) and AgZnS (701.2 µmole/g). Such a significant hydrogen evolution amount far exceeded that of undoped TiO2 and RGO. The H2 evolution amounts increased significantly at ultrasonic irradiation power of 80 MHz. AgZnS-G-T demonstrates the higher H2 evolution amounts of 985 µmole/g at 80 MHz. Its photocatalytic hydrogen-evolution activity remained at a high level over four cycles (16 h) nanoparticle.

Synthesis of LiDAR-Detectable True Black Core/Shell Nanomaterial and Its Practical Use in LiDAR Applications.

Light detection and ranging (LiDAR) sensors utilize a near-infrared (NIR) laser with a wavelength of 905 nm. However, LiDAR sensors have weakness in detecting black or dark-tone materials with light-absorbing properties. In this study, SiO2/black TiO2 core/shell nanoparticles (SBT CSNs) were designed as LiDAR-detectable black materials. The SBT CSNs, with sizes of 140, 170, and 200 nm, were fabricated by a series of Stöber, TTIP sol-gel, and modified NaBH4 reduction methods. These SBT CSNs are detectable by a LiDAR sensor and, owing to their core/shell structure with intrapores on the shell (ca. 2−6 nm), they can effectively function as both color and NIR-reflective materials. Moreover, the LiDAR-detectable SBT CSNs exhibited high NIR reflectance (28.2 R%) in a monolayer system and true blackness (L* < 20), along with ecofriendliness and hydrophilicity, making them highly suitable for use in autonomous vehicles.

Comparative and Efficient Ammonia Gas Sensing Study with Self-assembly-Synthesized Metal Oxide-SiC Fiber-Based Mesoporous SiO2 Composites.

Self-assembled-assisted ternary nanocomposite In2O3-SiC, CuO2-SiC, and MnO2-SiC semiconductors were mixed with SiO2 to enable gas sensing using cyclic voltammetry. The results of TEM (transm In2O3-SiC-SiO2 ion electron microscopy), X-ray diffraction spectroscopy, and Raman spectra analysis affirm the closeness of few layers between SiO2 and SiC in In2O3-SiC, MnO2-SiC, and CuO2-SiC. Among the electrochemical impedance spectra curves of the nanocomposites, none of the samples had a semicircle profile, which indicates the existence of a higher charge-transfer resistivity behavior between the electrolyte and the sample electrode with charge carrier and transport effects, which is related to the well-developed porous structure of synthesized composites. CuO2-SiC-SiO2 and MnO2-SiC-SiO2 showed high resistivity and a quite significant response for NH3 gas at room temperature. While there was a response for NH3 gas for In2O3-SiC-SiO2, the sensor showed a low response for the gas. From the sensing test, correspondences between the chemical structure of the sensor and the molecular structure of the gases have been found. The surface reactions between the sensor surface and the gas with a pore structure, along with the electron receiver/donor phase are observed from the results of gas sensor tests, and all factors are determining the precise state. Finally, the adsorption of NH3 molecules and the alteration of the electronic resistance of In2O3-SiC-SiO2, MnO2-SiC-SiO2, and CuO2-SiC-SiO2 were presented that include various thicknesses of charge to represent which are achieved by the connection with the substrates and the particles.

Development of Novel Colorful Electrorheological Fluids.

Herein, the electrorheological (ER) performances of ER fluids were correlated with their colors to allow for the visual selection of the appropriate fluid for a specific application using naked eyes. A series of TiO2-coated synthetic mica materials colored white, yellow, red, violet, blue, and green (referred to as color mica/TiO2 materials) were fabricated via a facile sol-gel method. The colors were controlled by varying the thickness of the TiO2 coating layer, as the coatings with different thicknesses exhibited different light interference effects. The synthesized color mica/TiO2 materials were mixed with silicone oil to prepare colored ER fluids. The ER performances of the fluids decreased with increasing thickness of the TiO2 layer in the order of white, yellow, red, violet, blue, and green materials. The ER performance of differently colored ER fluids was also affected by the electrical conductivity, dispersion stability, and concentrations of Na+ and Ca2+ ions. This pioneering study may provide a practical strategy for developing new ER fluid systems in future.