Few layered GeAs nanosheets exhibit a band gap of 2.1 eV, corresponding to that of monolayer predicted from first-principles calculations.

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 NiSe, cubic phase NiSe, 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 NiSe NCs are more metallic and form less surface oxides. As a result, the orthorhombic NiSe 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 NiSe. The remarkable bifunctional photocatalytic activity of orthorhombic NiSe promises efficient PEC water splitting.

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.

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 (TaN) nanocrystals as promising photoanode materials for visible-light-driven photoelectrochemical (PEC) water splitting cells. The surface of TaN 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 TaN 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 TaN nanocrystals, by catalyzing effectively the water splitting reaction.

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Recently, sodium ion batteries have attracted considerable interest for large-scale electric energy storage as an alternative to lithium ion batteries. However, the development of anode materials with long cycle life, high rate, and high reversible capacity is necessary for the advancement of sodium ion batteries. Bi anode is a promising candidate for sodium ion batteries due to its high theoretical capacity (385 mAh g–1 or 3800 mAh l–1) and high electrical conductivity (7.7 × 105 S m –1). Herein, we report the preparation of Bi anode using micro-sized commercial Bi particles. DME-based electrolyte was used, which is well known for its high ionic conductivity. The Bi anode showed excellent rate-capability up to 16 C-rate, and long cycle life stability with a high reversible capacity of 354 mAh g–1 at 16 C-rate for 50 cycles.

In this study, a passive sampler for gaseous elemental mercury (GEM) was developed and applied to field monitoring. Three Radiello® diffusive bodies with gold-coated beads as Hg adsorbent were installed in an acrylic external shield. Hg uptake mass linearly increased as the deployment time increased until 8 weeks with an average gaseous Hg concentration of 2 ng m−3. The average of the experimental sampling rate (SR) was 0.083 m3 day−1 and showed a good correlation with theoretical SRs, indicating that a major adsorption mechanism was molecular diffusion. Nonetheless, the experimental SR was approximately 33% lower than the modeled SR, which could be associated with inefficient uptake of GEM in the sampler or uncertainty in constraining model parameters. It was shown that the experimental SR was statistically affected by temperature and wind speed but the calibration equation for the SR by meteorological variables should be obtained with a wider range of variables in further investigation. When the uptake rates were compared to the active Hg measurements, the correlation was not significant because the passive sampler was not sufficiently adept at detecting a small difference in the GEM concentration of from 1.8 to 2.0 ng m−3. However, the results for spatial Hg concentrations measured near cement plants in Korea suggest a possible application in field monitoring. Future research is needed to fully employ the developed passive sampler in quantitative assessment of Hg concentrations.

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