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The design of efficient visible-light-driven photocatalysts has become a hot topic due to their potential applications in energy and environmental industries. In this work, sandwiched ZnO@Au@Cu2O nanorod films were prepared on stainless steel mesh substrates in the order of the following steps: electrodeposition, sputtering, and second electrodeposition. The as-synthesized nanocomposites were characterized by X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscopy, and UV-visible spectrophotometry, respectively. Due to their coaxial structure to inhibit the carrier recombination and the localized surface plasmon resonance effect of Au nanoparticles to enhance the visible light absorption, an outstanding visible-light-driven photocatalytic performance is realized. The enhancement magnitude of Au nanoparticles on the catalytic performance of ZnO@Au@Cu2O was estimated as a function of the Cu2O loading amount. The corresponding enhancement mechanism was also explained according to the photocatalytic results under monochromatic visible light irradiation, the active species trapping experiments, and discrete dipole approximation simulation results.

Dielectric oxides are traditionally used to fabricate resistive surface humidity-sensing devices, as well as capacitive sandwich-structured sensors. In the present work, relative humidity (RH) sensors were fabricated by employing vertically aligned TiO(2) nanotubes array (TNA) film produced using electro-chemical anodization of Ti foil followed by a nitrogen-doping process, simultaneously showing resistive and capacitive humidity-sensing properties in the range of 11.3-93.6%. For the sample formed at optimized experimental conditions, the capacitance (C(S)) and resistance (R(S)) of the as-fabricated RH sensors made from nitrogen-doped TiO(2) nanotubes film could be simultaneously obtained. Both the resistive and capacitive sensitivity (K(R) and K(C)) of the as-fabricated TiO(2) nanotube RH sensors show distinct dependence on the frequency of alternating current (AC) voltage signal and RH. At higher water coverage, water-water interaction will result in lowering of the water dissociation barrier, leading to an increase of conductance. With the increase of RH, the polarization of as-adsorbed water molecules will also occur, causing a sharp increase of capacitance. For an explanation of the frequency response of both C(S) and R(S), ionic transport, as well as the polarization effect, should be comprehensively considered. The changes of capacitance and resistance at different temperatures are plausibly caused by thermal expansion and surface state modification by adsorption and desorption of oxygen and water.

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Aligned carbon nanofibers (CNFs) with a population density of about 3 × 108 cm−2 are synthesized on electrochemically roughened silicon using the bias-assisted chemical vapor deposition system. Isolated CNFs with much lower population density (∼3 × 106 cm−2) are formed on polished silicon wafer at the same growth conditions. The morphologies, microstructures, and components of the CNFs are accordingly characterized using scanning electron microscopy, Raman spectroscopy, transmission electron microscopy, and energy dispersive analysis of X-rays. On the basis of the surface barrier limited diffusion model, it is shown that electrochemical roughening of silicon surface can increase the population density of energetic carbon species that act as self-catalysts for the vertical growth of CNFs. The formation of CNFs with cone-shaped tips simultaneously involves the vertical growth and a continuous thinning of fiber tips by the bombarding of CH4 + and H+ ions in CH4/H2 plasma.

For sensitive detection of H2, ZnO nanowires networks decorated with photo-decomposed Pd nanoparticles were fabricated between femtosecond laser-writing interdigitated electrodes by chemical vapor deposition method. When H2 concentration is increased from 20 to 4000 ppm at room temperature, sensitivity of the sample is increased from 3.7% to 1017.9%. The high sensitivity can be explained by considering the reaction between the adsorbed O2- and the disassociated H atoms facilitated by Pd nanoparticles. This mechanism is further supported by the H2 response results under UV light illumination, which can reduce the amount of O2- on the ZnO surface, leading to depressed sensitivity. The sensor also shows high selectivity, long-term stability, and ultra-low power consumption of nanowatt level, due to the novel fabrication process.

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TiO2 nanostructures are widely used for H2 detection in scientific and technological research fields, but how to detect ppm-level H2 in a timely and sensitive manner at room temperature remains challenging.