Orthorhombic NiSe2 Nanocrystals on Si Nanowires for Efficient Photoelectrochemical Water Splitting.

Photocatalytic water splitting is a vital technology for clean renewable energy. Despite enormous progress, the search for earth-abundant photocatalysts with long-term stability and high catalytic activity is still an important issue. We report three possible polymorphs of nickel selenide (orthorhombic phase NiSe2, cubic phase NiSe2, and hexagonal phase NiSe) as bifunctional catalysts for water-splitting photoelectrochemical (PEC) cells. Photocathodes or photoanodes were fabricated by depositing the nickel selenide nanocrystals (NCs) onto p- or n-type Si nanowire arrays. Detailed structural analysis reveals that compared to the other two types, the orthorhombic NiSe2 NCs are more metallic and form less surface oxides. As a result, the orthorhombic NiSe2 NCs significantly enhanced the performance of water-splitting PEC cells by increasing the photocurrents and shifting the onset potentials. The high photocurrent is ascribed to the excellent catalytic activity toward water splitting, resulting in a low charge-transfer resistance. The onset potential shift can be determined by the shift of the flat-band potential. A large band bending occurs at the electrolyte interface, so that photoelectrons or photoholes are efficiently generated to accelerate the photocatalytic reaction at the active sites of orthorhombic NiSe2. The remarkable bifunctional photocatalytic activity of orthorhombic NiSe2 promises efficient PEC water splitting.

Surface-Modified Ta3N5 Nanocrystals with Boron for Enhanced Visible-Light-Driven Photoelectrochemical Water Splitting.

Photocatalysts for water splitting are the core of renewable energy technologies, such as hydrogen fuel cells. The development of photoelectrode materials with high efficiency and low corrosivity has great challenges. In this study, we report new strategy to improve performance of tantalum nitride (Ta3N5) nanocrystals as promising photoanode materials for visible-light-driven photoelectrochemical (PEC) water splitting cells. The surface of Ta3N5 nanocrystals was modified with boron whose content was controlled, with up to 30% substitution of Ta. X-ray photoelectron spectroscopy revealed that boron was mainly incorporated into the surface oxide layers of the Ta3N5 nanocrystals. The surface modification with boron increases significantly the solar energy conversion efficiency of the water-splitting PEC cells by shifting the onset potential cathodically and increasing the photocurrents. It reduces the interfacial charge-transfer resistance and increases the electrical conductivity, which could cause the higher photocurrents at lower potential. The onset potential shift of the PEC cell with the boron incorporation can be attributed to the negative shift of the flat band potential. We suggest that the boron-modified surface acts as a protection layer for the Ta3N5 nanocrystals, by catalyzing effectively the water splitting reaction.

Low Dark-Current, High Current-Gain of PVK/ZnO Nanoparticles Composite-Based UV Photodetector by PN-Heterojunction Control.

We propose a solution-processable ultraviolet (UV) photodetector with a pn-heterojunction hybrid photoactive layer (HPL) that is composed of poly-n-vinylcarbazole (PVK) as a p-type polymer and ZnO nanoparticles (NPs) as an n-type metal oxide. To observe the effective photo-inducing ability of the UV photodetector, we analyzed the optical and electrical properties of HPL which is controlled by the doping concentration of n-type ZnO NPs in PVK matrix. Additionally, we confirmed that the optical properties of HPL dominantly depend on the ZnO NPs from the UV-vis absorption and the photoluminescence (PL) spectral measurements. This HPL can induce efficient charge transfer in the localized narrow pn-heterojunction domain and increases the photocurrent gain. It is essential that proper doping concentration of n-type ZnO NPs in polymer matrix is obtained to improve the performance of the UV photodetector. When the ZnO NPs are doped with the optimized concentration of 3.4 wt.%, the electrical properties of the photocurrent are significantly increased. The ratio of the photocurrent was approximately 10³ higher than that of the dark current.

Pharmacokinetic modeling of phagocytic activity of the liver using superparamagnetic iron oxide nanoparticles in dynamic MR imaging.

The purpose of this study was to determine whether phagocytic activity is measurable by dynamic superparamagnetic iron oxide-enhanced MR imaging. For these experiments on New Zealand White rabbits, which were randomly allocated to normal and silica treated groups, we performed a dynamic MR study and radioisotope study with Tc99m-phytate. In this dynamic MR study, the ratio (Rv) of the distribution volumes of iron oxide (Vm/Ve) could be obtained by applying three- compartment model to the data obtained from the kidney and liver simultaneously. Changes in Rv caused by silica injection and by dosing superparamagnetic iron oxide, AMI-25, were evaluated. In the dynamic MR study using a Beagle dog model the input function could be calculated from data obtained from the hepatic artery and portal vein. Rv's reached maximum values at around 80 minutes after the AMI-25 injection. The Rv of the normal group was 5.06 +/- 1.53 whereas the Rv of the silica treated group was 2.13 +/- 1.20. The results were similar to tissue count data obtained by radioisope study. The Rv value was not dependent on the injected dose of AMI-25. The rate of transport constants (k1, k2, k3) could not be estimated using the 3 compartment model regardless of obtaining the input function. We conclude that Rv may be an quantitative index of decreased phagocytic activity in the liver as determined by dynamic superparamagnetic iron oxide- enhanced MRI.