RESUMEN
The highly selective detection of trace gases using transparent sensors at room temperature remains challenging. Herein, transparent nanopatterned chemiresistors composed of aligned 1D Au-SnO2 nanofibers, which can detect toxic NO2 gas at room temperature under visible light illumination is reported. Ten straight Au-SnO2 nanofibers are patterned on a glass substrate with transparent electrodes assisted by direct-write, near-field electrospinning, whose extremely low coverage of sensing materials (≈0.3%) lead to the high transparency (≈93%) of the sensor. The sensor exhibits a highly selective, sensitive, and reproducible response to sub-ppm levels of NO2 , and its detection limit is as low as 6 ppb. The unique room-temperature NO2 sensing under visible light emanates from the localized surface plasmonic resonance effect of Au nanoparticles, thereby enabling the design of new transparent oxide-based gas sensors without external heaters or light sources. The patterning of nanofibers with extremely low coverage provides a general strategy to design diverse compositions of gas sensors, which can facilitate the development of a wide range of new applications in transparent electronics and smart windows wirelessly connected to the Internet of Things.
RESUMEN
Nanoporous Al2O3 substrates with an average pore size of about 150 nm were prepared via anodization of Aluminum plates. Depending on the anodization condition, the surface area of the anodized Al2O3 was increased more than six-fold. Solution-combusted ZnO nanopowders were prepared as a function of fuel/oxidant ratios. At a fuel/oxidant ratio of 0.8, ZnO powder showed excellent powder characteristics such as average particle sizes of 30 nm and spherical shape. Electrical properties of SCM ZnO nanopowders with different fuel/oxidant ratios were investigated by Hall measurement. The carrier concentration of SCM ZnO nanopowders at the fuel/oxidant ratio of 0.8, was the highest, three-fold higher than that of any commercial ZnO powders. Using spray coating, these nanopowders were coated onto Al2O3 substrates for immobilization. To evaluate the photo-catalytic effect, Ag ions were removed from the wastewater via photocatalysis. The photocatalytic efficiency with the SCM ZnO nanopowders on nanoporous Al2O3 substrates was 2.5-fold higher than that with the SCM ZnO nanopowders on normal Al2O3 substrates. However, commercial zinc oxide powders did not show any photocatalytic phenomena. The large difference in photocatalytic efficiency was probably attributed to the characteristics of SCM ZnO nanopowder and the large surface area of anodized Al2O3.
RESUMEN
Pure and 3-12 at. % Pr-doped In2O3 macroporous spheres were fabricated by ultrasonic spray pyrolysis and their acetone-sensing characteristics under dry and humid conditions were investigated to design humidity-independent gas sensors. The 12 at. % Pr-doped In2O3 sensor exhibited approximately the same acetone responses and sensor resistances at 450 °C regardless of the humidity variation, whereas the pure In2O3 exhibited significant deterioration in gas-sensing characteristics upon the change in the atmosphere, from dry to humid (relative humidity: 80%). Moreover, the 12 at. % Pr-doped In2O3 sensor exhibited a high response to acetone with negligible cross responses to interfering gases (NH3, CO, benzene, toluene, NO2, and H2) under the highly humid atmosphere. The mechanism for the humidity-immune gas-sensing characteristics was investigated by X-ray photoelectron and diffuse reflectance infrared Fourier transform spectroscopies together with the phenomenological gas-sensing results and discussed in relation with Pr3+/Pr4+ redox pairs, regenerative oxygen adsorption, and scavenging of hydroxyl groups.
RESUMEN
Nano-sized powders of ZnO phosphor were prepared by a solution combustion method (SCM). The ZnO powder prepared using Zn(OH)2 and glycine as the oxidant and fuel, respectively, (fuel/oxidant = 0.8), show good powder characteristics such as an average grain size of 30 nm and specific surface area of 120 m²/g. Single-phase ZnO powders were obtained regardless of the fuel/ oxidant ratio. The photoluminescence spectra of the obtained ZnO powders show a single sharp peak near 390 nm corresponding to a deep blue color. This was confirmed by cathodoluminescence measurement and CIE color coordinate values. The PL spectra, powder characteristics and electrical properties show very good consistency. Furthermore, the electron carrier concentration of the ZnO nanopowders prepared by SCM is more than 3 orders of magnitude higher than that of the purest ZnO single crystal, which is commercially available. These powders could be potentially applied as blue phosphors of displays such as A.C. powder electroluminescent devices and plasma display panels.
RESUMEN
Co3O4 sensors with a nanoscale TiO2 or SnO2 catalytic overlayer were prepared by screen-printing of Co3O4 yolk-shell spheres and subsequent e-beam evaporation of TiO2 and SnO2. The Co3O4 sensors with 5 nm thick TiO2 and SnO2 overlayers showed high responses (resistance ratios) to 5 ppm xylene (14.5 and 28.8) and toluene (11.7 and 16.2) at 250 °C with negligible responses to interference gases such as ethanol, HCHO, CO, and benzene. In contrast, the pure Co3O4 sensor did not show remarkable selectivity toward any specific gas. The response and selectivity to methylbenzenes and ethanol could be systematically controlled by selecting the catalytic overlayer material, varying the overlayer thickness, and tuning the sensing temperature. The significant enhancement of the selectivity for xylene and toluene was attributed to the reforming of less reactive methylbenzenes into more reactive and smaller species and oxidative filtering of other interference gases, including ubiquitous ethanol. The concurrent control of the gas reforming and oxidative filtering processes using a nanoscale overlayer of catalytic oxides provides a new, general, and powerful tool for designing highly selective and sensitive oxide semiconductor gas sensors.
RESUMEN
Co3O4 hollow spheres prepared by ultrasonic spray pyrolysis were converted into Co3O4-SnO2 core-shell hollow spheres by galvanic replacement with subsequent calcination at 450 °C for 2 h for gas sensor applications. Gas selectivity of the obtained spheres can be controlled by varying the amount of SnO2 shells (14.6, 24.3, and 43.3 at. %) and sensor temperatures. Co3O4 sensors possess an ability to selectively detect ethanol at 275 °C. When the amount of SnO2 shells was increased to 14.6 and 24.3 at. %, highly selective detection of xylene and methylbenzenes (xylene + toluene) was achieved at 275 and 300 °C, respectively. Good selectivity of Co3O4 hollow spheres to ethanol can be explained by a catalytic activity of Co3O4; whereas high selectivity of Co3O4-SnO2 core-shell hollow spheres to methylbenzenes is attributed to a synergistic effect of catalytic SnO2 and Co3O4 and promotion of gas sensing reactions by a pore-size control of microreactors.