Hierarchical nanostructures with much increased surface-to-volume ratio have been of significant interest for prototypical gas sensors. Herein we report a novel resistive gas sensor based on TiO2/V2O5 branched nanoheterostructures fabricated by a facile one-step synthetic process, in which well-matched energy levels induced by the formation of effective heterojunctions between TiO2 and V2O5, a large Brunauer-Emmett-Teller surface area and complete electron depletion for the V2O5 nanobranches induced by the branched-nanofiber structures are all beneficial to the change of resistance upon ethanol exposure. As a result, the ethanol sensing performance of this device shows a lower operating temperature, faster response/recovery behavior, better selectivity and about seven times higher sensitivity compared with pure TiO2 nanofibers. This study not only confirms the gas sensing mechanism for performing enhancement of branched nanoheterostructures, but also proposes a rational approach to the design of nanostructure-based chemical sensors with desirable performance.
Traditionally, densification and grain growth are two competing processes in sintering of ceramics. To improve the density, while limiting grain growth at the same time, an ultrahigh pressure (>1 GPa) is employed here and results in plastic deformation as the dominant densification mechanism during the sintering process. In this way, fully dense boron carbide (B4C) structural ceramics without grain growth is prepared under the pressure of 4.5 GPa at low temperature of 1300°C in 5 minutes, while showing excellent mechanical properties such as Vickers hardness of 38.04 GPa, Young's modulus of 487.7 GPa, and fracture toughness of 3.87 MPa·m1/2. This study should also facilitate the development of other structural ceramics for practical applications.
Under shock pressures up to 210 GPa, we measured the refractive index of sapphire at a wavelength of 1550 nm by performing plate impact experiments in order to investigate its refractive-index change behaviors and phase transitions along the Hugoniot state. There were two discontinuities in the refractive index at ∼65 to 92 GPa and ∼144 to 163 GPa, respectively. Moreover, above the Hugoniot elastic limit, the pressure dependence of the refractive index was divided into three segments, and there were large differences in their pressure-change trends: the refractive index decreased evidently with pressure in the first segment (∼20 to 65 GPa), remained nearly constant from ∼92 to ∼144 GPa in the second segment, and obviously increased with pressure in the last segment (∼163 to 210 GPa). Our first-principles calculations suggest that the observed discontinuities were closely related to the corundum-Rh2O3(II) and Rh2O3(II)-CaIrO3 structural transitions, and the shock-induced vacancy point defects could be one factor causing these great discrepancies in pressure-change trends. This work provides sapphire refractive-index information in a megabar-pressure range and clear evidence of its shock structural transitions. This not only has a great significance for the velocity correction of laser interferometer experiments and the analysis of sapphire high-pressure properties but also indicates a possible approach to explore the shock transitions of transparent materials.
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