Synthesis and Photocatalytic Property of Hectorite/(Pt,TiO2) and H4Nb6O17/(Pt,TiO2) Nanocomposites

Abstract

TiO₂ and Pt have been intercalated in hectorite and H₄Nb₆O₁₇. The height of TiO₂ and Pt pillars was less than 0.8 nm and the band gap energy of TiO₂ pillars was ca. 3.3 eV. Both hectorite/TiO₂ and H₄Nb₆O₁₇(Pt, TiO₂) were capable of hydrogen evolution following irradiation from a high pressure mercury are (λ > 290 nm) in the presence of methanol as a sacrificial hole acceptor and the hydrogen evolution was enhanced by co-incorporation of Pt, although hectorite and hectorite/Pt did not show photocatalytic activity. Incorporation of Pt or Pt and TiO₂ in the interlayer of H₄Nb₆O₁₇ has resulted in enhanced photo evolution of hydrogen, however, TiO₂ alone in the interlayer of H₄Nb₆O₁₇ showed adverse photocatalytic activity.     

Study of Si(0 0 1)4 × 2-Ga structure by scanning tunneling microscopy and ab initio calculation

We have studied Si(0 0 1)-Ga surface structures formed at Ga coverages of slightly above 0.50 monolayer (ML) at 250 °C by scanning tunneling microscopy (STM). 4 × 2-, 5 × 2-, and 6 × 2-Ga structures were observed in a local area on the surface. The 4 × 2-Ga structure consists of three protrusions, as observed in filled- and empty-state STM images. The characters of these structures are clearly different from those of other Si(0 0 1)-Ga structures. We also performed an ab initio calculation of the energetics for several possible models for the 4 × 2-Ga structure, and clarified that the three-orthogonal-Ga-dimer model is the most stable. Also, the results of comparing the simulated STM images and observation images at various bias voltages indicate that this structural model is the most favorable.     

Simulation of flux dynamics in a superconducting bulk magnetized by multi-pulse technique

We have simulated the time and spatial dependence of local field B_z(t, r) and temperature T(t, r) on the superconducting bulk during pulsed field magnetization (PFM) using the finite element method (FEM). A modified multi-pulse technique with step-wise cooling (MMPSC) was performed to the cryo-cooled bulk, which was experimentally confirmed to the effective PFM technique to enhance the trapped field B_z higher than 5 T. In the simulation, the B_z value at the center of the bulk surface was enhanced at the 2nd stage of the MMPSC method, in which the results of the simulation reproduced the experimental ones. The enhancement of B_z results from the reduction in the temperature because of the already trapped flux in the bulk at the 1st stage of the MMPSC method.     

Selection of spectral lines and transition probability data in plasma temperature measurements by photoelectric scanning spectrometry

A strict, comparative investigation of published transition probabilities for thermometric lines and an experimental study of determinations of plasma temperatures were made for improving the accuracy in temperature measurements by the well-known slope method. Four sets of FeI lines which satisfy the requirements for the thermometric lines were selected in the wavelength region of 200–400 nm. A statistical method was used to evaluate degrees of agreement among different sets of transition probabilities. In the experimental study, excitation temperatures of a stabilized arc plasma were determined from relative line-intensities recorded by photoelectric scanning spectrometry. In conclusion, two recommended combinations of lines and transition probability data are presented for the slope temperature measurement. Line pairs used in combination of selected transition probabilities suitable for the two-line method are also given.     

Approximate controllability for fractional diffusion equations by interior control

We consider the approximate controllability by interior control of a partial differential equation with time derivatives of non-integer order. First, we prove the well-posedness of the inhomogeneous problem for the controlled system. Next, we study the dual system and show a weak type of unique continuation property. Finally, we prove the approximate controllability.     

Fabrication and characterization of high performance cathode supported small-scale SOFC for intermediate temperature operation

A high performance small-scale solid oxide fuel cell supported by a microtubular cathode was successfully developed via the extrusion of a (La_0.8Sr_0.2)_0.97MnO₃ cathode support and subsequent surface coating with a (La_0.8Sr_0.2)_0.97MnO₃–Ce_0.9Gd_0.1O_1.95 activation layer followed by Sc₂O₃-doped ZrO₂ electrolyte and NiO–Ce_0.9Gd_0.1O_1.95 anode slurries. The cell was electrochemically evaluated in a humidified hydrogen (3% H₂O) atmosphere, and exhibited a stable open circuit voltage above 1.05 V in the temperature range from 550 to 750 °C. Maximum power densities of 46.5, 163.2 and 452.8 mW cm⁻² were generated at 550, 650 and 750 °C, respectively. The results indicate the realization of a stable and high performance cathode-supported micro SOFC.     

Identification of HcgC as a SAM‐Dependent Pyridinol Methyltransferase in [Fe]‐Hydrogenase Cofactor Biosynthesis

Previous retrosynthetic and isotope‐labeling studies have indicated that biosynthesis of the iron guanylylpyridinol (FeGP) cofactor of [Fe]‐hydrogenase requires a methyltransferase. This hypothetical enzyme covalently attaches the methyl group at the 3‐position of the pyridinol ring. We describe the identification of HcgC, a gene product of the hcgA‐G cluster responsible for FeGP cofactor biosynthesis. It acts as an S‐adenosylmethionine (SAM)‐dependent methyltransferase, based on the crystal structures of HcgC and the HcgC/SAM and HcgC/S‐adenosylhomocysteine (SAH) complexes. The pyridinol substrate, 6‐carboxymethyl‐5‐methyl‐4‐hydroxy‐2‐pyridinol, was predicted based on properties of the conserved binding pocket and substrate docking simulations. For verification, the assumed substrate was synthesized and used in a kinetic assay. Mass spectrometry and NMR analysis revealed 6‐carboxymethyl‐3,5‐dimethyl‐4‐hydroxy‐2‐pyridinol as the reaction product, which confirmed the function of HcgC.     

Electrochemical reactors for NO decomposition. Basic aspects and a future

The electrochemical reduction of nitric oxide in the presence of the excess oxygen was reviewed. It was shown that the selectivity and activity of the cathodes is strongly dependent on the composition and on the microstructure of the cathode material. A concept of electrochemical reactor with multilayer electro-catalytic electrode was proposed and successfully designed in Advanced Manufacturing Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Nagoya, Japan. The typical values of current efficiency in such electrochemical reactors are of the order of 10–20% at gas composition: 1,000 ppm NO and 2% O₂ balanced in He and at gas flow rate 50 ml/min. The value of current efficiency depends on the functional multi-layer electrode composition, structure, and operating temperature. Such electrochemical reactors show the value of NO/O₂ selectivity (ν _sel) higher than 5 (ν _sel > 5) at intermediate temperature and up to ν _sel = 25 at low temperature operation. It was shown that multilayer electro-catalytic electrode should consist at list from three main functional layers: cathode, electro-catalytic electrode, covering layer, in order to operate as an electrode with high selectivity.