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An anatase TiO2 film sensor was prepared by a facile in-situ method on the interdigitated Au electrode deposited on the alumina substrate. The structure, morphology and the optical properties of the in-situ TiO2 film sensor were characterized by X-ray diffraction, Scanning Electron Microscopy, and UV-vis diffuse reflectance spectra. The photo-assisted gas sensitivities of the prepared film towards H2 gas were evaluated at room temperature in N2 and synthetic air atmospheres. As compared to TiO2 film sensor prepared by drop-coating method, this in-situ TiO2 film sensor exhibited a more compact structure composed of uniform TiO2 microspheres as well as a better gas sensitivity towards H2 under UV irradiation, especially in synthetic air. The photo-electrochemical measurements suggest that these improvements may be associated with the efficient charge transfer in the TiO2 interface induced by the TiO2 microsphere structure. This study might offer a feasible approach to develop photo-assisted gas sensors at ambient temperature. [ABSTRACT FROM AUTHOR]

Solid-state dye-sensitized solar cells (ssDSSC) constitute a major approach to photovoltaic energy conversion with efficiencies over 8% reported thanks to the rational design of efficient porous metal oxide electrodes, organic chromophores, and hole transporters. Among the various strategies used to push the performance ahead, doping of the nanocrystalline titanium dioxide (TiO2) electrode is regularly proposed to extend the photo-activity of the materials into the visible range. However, although various beneficial effects for device performance have been observed in the literature, they remain strongly dependent on the method used for the production of the metal oxide, and the influence of nitrogen atoms on charge kinetics remains unclear. To shed light on this open question, we synthesized a set of N-doped TiO2 nanopowders with various nitrogen contents, and exploited them for the fabrication of ssDSSC. Particularly, we carefully analyzed the localization of the dopants using X-ray photo-electron spectroscopy (XPS) and monitored their influence on the photo-induced charge kinetics probed both at the material and device levels. We demonstrate a strong correlation between the kinetics of photo-induced charge carriers probed both at the level of the nanopowders and at the level of working solar cells, illustrating a direct transposition of the photo-physic properties from materials to devices. [ABSTRACT FROM AUTHOR]

A reversible photo-, thermal-, and pH-responsive high-performance functional wood with fluorescence has been prepared. The properties, structure, multi-response, fluorescence, water resistance, and corrosion resistance of original wood (ORW) and functional wood (FUW) were investigated with an X-ray photoelectron spectroscopy (XPS) spectrometer, a Fourier-transform infrared (FTIR) spectrometer, a N2 adsorption–desorption analyzer, an atomic force microscope (AFM), tensile tests, a scanning electron microscope (SEM), an ultraviolet–visible (UV–Vis) spectrophotometer, a fluorescence spectrometer, the equilibrium swelling ratio (ESR), and corrosion tests. The results of XPS, FTIR, N2 adsorption–desorption, and AFM exhibited that FUW was successfully prepared. Additionally, the results of the tensile test and SEM revealed that FUW had better mechanical properties than ORW, due to the filling of epoxy resin in the pores of the wood. Moreover, the UV–Vis and fluorescence spectra demonstrated that the introduction of epoxy resin induced multi-response and fluorescence functions to FUW. Furthermore, the data of ESR and corrosion test showed that the introduction of epoxy resin greatly improved the water and corrosion resistance of wood. This study provides ideas and methods for preparing novel high-performance multi-response FUW. [ABSTRACT FROM AUTHOR]

We report an investigation on the photo-response from a GeSn-based photodetector using a tunable laser with a range of incident light power. An exponential increase in photocurrent and an exponential decay of responsivity with increase in incident optical power intensity were observed at higher optical power range. Time-resolved measurement provided evidence that indicated monomolecular and bimolecular recombination mechanisms for the photo-generated carriers for different incident optical power intensities. This investigation establishes the appropriate range of optical power intensity for GeSn-based photodetector operation. [ABSTRACT FROM AUTHOR]

An anatase TiO₂ film sensor was prepared by a facile in-situ method on the interdigitated Au electrode deposited on the alumina substrate. The structure, morphology and the optical properties of the in-situ TiO₂ film sensor were characterized by X-ray diffraction, Scanning Electron Microscopy, and UV-vis diffuse reflectance spectra. The photo-assisted gas sensitivities of the prepared film towards H₂ gas were evaluated at room temperature in N₂ and synthetic air atmospheres. As compared to TiO₂ film sensor prepared by drop-coating method, this in-situ TiO₂ film sensor exhibited a more compact structure composed of uniform TiO₂ microspheres as well as a better gas sensitivity towards H₂ under UV irradiation, especially in synthetic air. The photo-electrochemical measurements suggest that these improvements may be associated with the efficient charge transfer in the TiO₂ interface induced by the TiO₂ microsphere structure. This study might offer a feasible approach to develop photo-assisted gas sensors at ambient temperature.