CuO nanowires have been prepared and applied for the fabrication of glucose sensors with highly enhanced sensitivity. Cu(OH)(2) nanowires were initially synthesised by a simple and fast procedure, CuO nanowires were then formed simply by removing the water through heat treatment. The structures and morphologies of Cu(OH)(2) and CuO nanowires were characterised by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy. The direct electrocatalytic oxidation of glucose in alkaline medium at CuO nanowire modified electrodes has been investigated in detail. Compared to a bare Cu electrode, a substantial decrease in the overvoltage of the glucose oxidation was observed at the CuO nanowire electrodes with oxidation starting at ca. 0.10 V vs. Ag/AgCl (saturated KCl). At an applied potential of 0.33 V, CuO nanowire electrodes produce high and reproducible sensitivity to glucose with 0.49 microA/micromol dm(-3). Linear responses were obtained over a concentration range from 0.40 micromol dm(-3) to 2.0 mmol dm(-3) with a detection limit of 49 nmol dm(-3) (S/N = 3). The CuO nanowire modified electrode allows highly sensitive, low working potential, stable, and fast amperometric sensing of glucose, thus is promising for the future development of non-enzymatic glucose sensors.

Converting light energy to electrical energy in photovoltaic devices relies on the photogenerated electrons and holes separated by the built-in potential in semiconductors. Photo-excited electrons in metal electrodes are usually not considered in this process. Here, we report an enhanced photovoltaic effect in the ferroelectric lanthanum-modified lead zirconate titanate (PLZT) by using low work function metals as the electrodes. We believe that electrons in the metal with low work function could be photo-emitted into PLZT and form the dominant photocurrent in our devices. Under AM1.5 (100 mW/cm2) illumination, the short-circuit current and open-circuit voltage of Mg/PLZT/ITO are about 150 and 2 times of those of Pt/PLZT/ITO, respectively. The photovoltaic response of PLZT capacitor was expanded from ultraviolet to visible spectra, and it may have important impact on design and fabrication of high performance photovoltaic devices based on ferroelectric materials.

When a Si photocathode is used in a photoelectrochemical cell for H2 production, an open nanostructure capable of enhanced light absorption, low surface recombination, and being fully protected by thin protective layer is highly desirable. Here, we explored a highly stable and efficient multi-crystalline (mc) n+p silicon photocathode. A pyramid-like surface nanostructure on mc-Si wafer was fulfilled through a two-step metal-catalyzed chemical etching process, and then a n+p junction photocathode protected by a thin Al2O3 layer was constructed. The photocathode exhibits a high stability of continuous photoelectrochemical H2 production for above 100 h after a thin layer of Al2O3 is coated on its surface, and its energy conversion efficiency can be up to 6.8% after Pt loading, due to the lowered surface light reflection, increased surface area and minority carrier life time on the electrode surface.

A novel nanostructured ferroelectric photovoltaic material, consisting of the ferroelectric lead zirconate titanate (PZT) film and Ag(2) O semiconductor nanoparticles of comparatively narrow bandgap, has demonstrated a remarkable enhancement in the photovoltaic effects and the highest light-electricity conversion efficiency among those PZT-based photodiodes previously reported. This work sheds light on the design and enhanced performance of new optoelectronic and solar energy devices.