Large-area vertical rutile TiO2 nanorod arrays (TNAs) were grown on F/SnO2 conductive glass using a hydrothermal method at low temperature. A self-powered ultraviolet (UV) photodetector based on TiO2 nanorod/water solid–liquid heterojunction is designed and fabricated. These nanorods offer an enlarged TiO2/water contact area and a direct pathway for electron transport simultaneously. By connecting this UV photodetector to an ammeter, the intensity of UV light can be quantified using the output short-circuit photocurrent without a power source. A photosensitivity of 0.025 A/W and a quick response time were observed. At the same time, a high photosensitivity in a wide range of wavelength was also demonstrated. This TNA/water UV detector can be a particularly suitable candidate for practical applications for its high photosensitivity, fast response, excellent spectral selectivity, uncomplicated low-cost fabrication process, and environment-friendly feature.

Nano-branched TiO2 arrays were fabricated on fluorine-doped tin oxide (FTO) glass by a facile two-step chemical synthesis process. Self-powered UV photodetectors based on photoelectrochemical cells (PECs) were assembled using these TiO2 nano-branched arrays as photoanodes. These visible-blind self-powered UV photodetectors exhibit high sensitivity and high-speed photoresponse. Compared with photodetectors based on bare TiO2 nanorod arrays, TiO2 nano-branched arrays show drastically improved photodetecting performance as photoanodes. The photosensitivity increases from 0.03 to 0.22 A W(-1) when optimized nano-branched TiO2 arrays are used, corresponding to an incident photon-to-current conversion efficiency higher than 77%. The UV photodetectors also exhibit excellent spectral selectivity and fast response (0.05 s decay time). The improved performance is attributed to a markedly enlarged TiO2/electrolyte contact area and good electron conductivity in the one-dimensional, well-aligned TiO2 nanorod trunk.

We have carried out a detailed investigation of the magnetism, valence state, and magnetotransport in VSe bulk single crystals, as well as in laminates obtained by mechanical exfoliation. In sharp contrast to the ferromagnetic behavior reported previously, here, no ferromagnetism could be detected for VSe single crystal and laminate from room temperature down to 2 K. Neither did we find the Curie paramagnetism expected due to the 3d odd-electronic configuration of covalent V ions. Rather, intrinsic VSe is a non-magnetic alloy without local moment. Only a weak paramagnetic contribution introduced by defects is noticeable below 50 K. A weak localization effect due to defects was also observed in VSe single crystals for the first time.

ZnO nanoneedle arrays were grown vertically on a fluorine-doped tin oxide-coated glass by hydrothermal method at a relatively low temperature. A self-powered photoelectrochemical cell-type UV detector was fabricated using the ZnO nanoneedles as the active photoanode and H2O as the electrolyte. This solid-liquid heterojunction offers an enlarged ZnO/water contact area and a direct pathway for electron transport simultaneously. By connecting this UV photodetector to an ammeter, the intensity of UV light can be quantified using the output short-circuit photocurrent without a power source. High photosensitivity, excellent spectral selectivity, and fast photoresponse at zero bias are observed in this UV detector. The self-powered behavior can be well explained by the formation of a space charge layer near the interface of the solid-liquid heterojunction, which results in a built-in potential and makes the solid-liquid heterojunction work in photovoltaic mode.

Self-powered UV photodetectors based on TiO2 and ZnO nanorod arrays have attracted lots of attention in recent years due to their various advantages. Impressive performances were observed in photochemical cell based UV detectors. However, liquid electrolytes are not ideal for long-term operation and are inconvenient for practical applications. Hence there is an urgent demand for replacing liquid electrolytes with solid-state hole transfer materials. Herein we report a nanostructured quasi-solid-state UV photodetector fabricated using a liquid crystal (LC)-embedded electrolyte with a light-trapping scheme. Vertical rutile TiO2 nanorod arrays grown on fluorine-doped tin oxide conductive glass were used as the active photoanode. A high incident photon-to-current conversion efficiency of 29% at 383 nm and a quick response time of less than 0.03 s were observed. In addition, it was revealed that the quasi-solid-state UV photodetector showed visible-blind, high responsivity, fast time response and good photosensitivity linearity in a wide light intensity range. The LC-embedded electrolyte with a light-trapping scheme enhanced the light absorption and thus improved the photodetecting performance. This self-powered device is a promising candidate for application in high-sensitivity and high-speed UV light photodetectors.