Two-Phase Synthesis of Fe Doped Cerium Phosphate Ultra-fine Nanocrystals for Efficient Oxygen Evolution

It is very important and challenging to develop electrocatalysts with high performance and economic benefits. In this work, ultra-fine Fe doped CePO4 nanocrystals (Fe-CePO4) were prepared by a simple two-step...

Application of a novel gas phase synthesis approach to carbonyl complexes of accelerator-produced 5d transition metals

In 2014 the first synthesis of a transactinide carbonyl complex – seaborgium hexacarbonyl – was reported. This was achieved in gas-phase chemical experiments in a beam-free environment behind the recoil separator GARIS. Extending this work to heavier elements requires more efficient techniques to synthesize carbonyl complexes as production rates of transactinide elements drop with increasing atomic number. A novel approach was thus conceived, which retains the benefit of a beam-free environment but avoids the physical preseparation step. The latter reduces the yields for products of asymmetric reactions such as those used for the synthesis of suitable isotopes of Sg, Bh, Hs and Mt. For this a series of experiments with accelerator-produced radioisotopes of the lighter homologues W, Re and Os was carried out at the tandem accelerator of JAEA Tokai, Japan. A newly developed double-chamber system, which allows for a decoupled recoil ion thermalization and chemical complex formation, was used, which avoids the low-efficiency physical preseparation step. Here, we demonstrate the feasibility of this newly developed method using accelerator-produced short-lived radioisotopes of the 5d homologues of the early transactinides.

Preparation of Magnetically Driven Nickel Phosphide Nanowires and Their Electrochemical Properties

In this study, nickel phosphide nanowires with various structures and compositions were fabricated for the first time via magnetically-assisted liquid phase synthesis. The curvature and aspect ratio of the nanowires largely depended on the strength of the magnetic field applied during synthesis. Their phosphorus content together with the morphology were significantly modified according to the pH and reducing agent concentration. Nanowires with different structures and phosphorus contents were preliminarily tested for their capabilities to serve in general electrochemical applications. The degree of reaction (i.e., amount of reaction charge) increased with increases in the reaction area and phosphorus content of the nanowires. The rate characteristics of the reaction showed a peculiar increasing trend for a small reaction surface area and low phosphorus content. A change in the ohmic overpotential according to the nanowire curvature (aspect ratio) and porosity was suggested to be the reason for this unusual trend. Electrodes with high phosphorus contents or high reaction surface areas rapidly deteriorated during repetitive redox reactions. Based on the results for the degradation degree, the effect of the reaction surface area dominated that of the phosphorus content in the deterioration of the nickel phosphide nanowires.