Depth-controlled reconstruction of 3D integral image using synthesized intermediate sub-images

In this paper, we propose a method that controls the depth of the three-dimensional (3D) object existing over the depth-of-focus in integral imaging. The depth control method is performed only in a computer by synthesizing the intermediate sub-images between original sub-images obtained by transforming the captured elemental images. In the reconstruction process, we can obtain reconstructed 3D images with the better image quality within depth-of-focus than that reconstructed over the depth-of-focus. To demonstrate the feasibility of our method, optical and computational experiments are carried out and its results are presented.     

First-principles computational approach for innovative design of highly functional electrocatalysts in fuel cells

Design of highly active and stable electrocatalyst is a major objective in a fuel cell. The special situation imposed to the electrocatalyst such as one of the most sluggish catalysis of oxygen reduction reaction, inherent structural instability of dispersed nanoparticle, harsh electrochemical conditions of electric potential and nonzero pH aqueous solution requires unique attention in the design. Considering that various attempts have been made for the purpose, high-speed but rigorous formalisms to evaluate the performance of candidates are crucial.This review article briefly introduces recently developed first-principles computational methodologies mainly applied to catalytic activity and electrochemical stability of electrocatalysts in proton exchange membrane fuel cells. Innovative design principles deduced from the outcomes are clearly discussed.     

Molecular Encapsulation of Trimeric Chromium Carboxylate Clusters in Metal–Organic Frameworks and Propylene Sorption

Oxo-bridged trimeric chromium acetate clusters [Cr₃O(OOCCH₃)₆(H₂O)₃]NO₃ have been encapsulated for the first time in the mesoporous cages of the chromium terephthalate MIL-101(Cr). The isolated clusters in MIL-101(Cr) have increased affinity towards propylene compared to propane, due to generation of a new kind of pocket-based propylene-binding site, as supported by DFT calculations.     

Activation of α-Fe2O3 for Photoelectrochemical Water Splitting Strongly Enhanced by Low Temperature Annealing in Low Oxygen Containing Ambient

Photoelectrochemical (PEC) water splitting is a promising method for the conversion of solar energy into chemical energy stored in the form of hydrogen. Nanostructured hematite (α-Fe₂O₃) is one of the most attractive materials for a highly efficient charge carrier generation and collection due to its large specific surface area and the short minority carrier diffusion length. In the present work, the PEC water splitting performance of nanostructured α-Fe₂O₃ is investigated which was prepared by anodization followed by annealing in a low oxygen ambient (0.03 % O₂ in Ar). It was found that low oxygen annealing can activate a significant PEC response of α-Fe₂O₃ even at a low temperature of 400 °C and provide an excellent PEC performance compared with classic air annealing. The photocurrent of the α-Fe₂O₃ annealed in the low oxygen at 1.5 V vs. RHE results as 0.5 mA cm⁻², being 20 times higher than that of annealing in air. The obtained results show that the α-Fe₂O₃ annealed in low oxygen contains beneficial defects and promotes the transport of holes; it can be attributed to the improvement of conductivity due to the introduction of suitable oxygen vacancies in the α-Fe₂O₃. Additionally, we demonstrate the photocurrent of α-Fe₂O₃ annealed in low oxygen ambient can be further enhanced by Zn-Co LDH, which is a co-catalyst of oxygen evolution reaction. This indicates low oxygen annealing generates a promising method to obtain an excellent PEC water splitting performance from α-Fe₂O₃ photoanodes.     

Gamma Vibrational Bands and Chiral Doublet Bands in A≈100 Neutron-rich Nuclei

The level structures of neutron-rich ~(105)Mo,~(106)Mo,~(108)Mo and 110Ru nuclei in A≈100 region have been carefully investigated by coincidence measurements of the prompt γ-rays populated in the spontaneous fission of ~(252)Cf with the Gammasphere detector array.In 105Mo,one-phonon K =9/2 and two-phonon K=13/2 γ-vibrational bands have been identified.In ~(108)Mo,one-phonon γ-vibrational band is expanded and two-phonon γ-vibrational band has been identified.Two similar sets of bands in ~(106)Mo and ~(110)Ru are observed to high spins,which have been proposed as the soft chiral γ-vibrational bands.The characteristics for these γ-vibrational bands and chiral doublet bands have been discussed.     

A dynamic approach to the Shapley value based on associated games

We propose a dynamic process leading to the Shapley value of TU games or any solution satisfying Inessential Game (IG) and Continuity (CONT), based on a modified version of Hamiache's notion of an associated game. The authors are very grateful to William Thomson and two anonymous referees for valuable comments which much improve the paper. They provide better statements and proofs of several major results than the original ones.     

Misalignment tolerance analysis and fabrication for highly efficient parallel optical-electrical convertor module

A compact, highly efficient, and passively assembled parallel optical-electrical convertor module (POECM) for active optical cable application is proposed. This paper presents our POECM structure, optical design simulation results, fabrication process, and data transmission test results, in sequence. The POECM has a compact size of \(18.5\hbox {mm} \times 10\hbox {mm} \times 2.8\hbox {mm}\) . We confirm a data rate of total throughput at 21.6 Gbps ( \(5.4\hbox {Gbps} \times 4\) channels) with a bit error rate of less than \(10^{-12}\) .     

Influence of TiO2 nanotube morphology and TiCl4 treatment on the charge transfer in dye-sensitized solar cells

Dye-sensitized solar cells (DSSCs) were fabricated using TiO₂ nanoparticles (NPs), TiO₂ nanotube arrays (NTAs), and surface-modified NTAs with a TiCl₄ treatment. The photovoltaic efficiencies of the DSSCs using TiO₂ NP, NTA, and TiCl₄-treated NTA electrodes are 4.25, 4.74, and 7.47 %, respectively. The highest performance was observed with a TiCl₄-treated TiO₂ NTA photoanode, although in the case of the latter two electrodes, the amounts of N719 dye adsorbed were similar and 68 % of that of the NP electrode. Electrochemical impedance measurements show that the overall resistance, including the charge–transfer resistance, was smaller with NTA morphologies than with NP morphologies. We suggest that a different electron transfer mechanism along the one-dimensional nanostructure of the TiO₂ NTAs contributes to the smaller charge–transfer resistance, resulting in a higher short circuit current (J _sc), even at lower dye adsorption. Furthermore, the TiCl₄-treated NTAs showed even smaller charge–transfer resistance, resulting in the highest J _sc value, because the downward shift in the conduction band edge improves the electron injection efficiency from the excited dye into the TiCl₄-treated TiO₂ electrodes.     

Study of alkyl chain length dependent characteristics of imidazolium based ionic liquids [CnMIM]+[TFSA]− by Brillouin and dielectric loss spectroscopy

This study examined the acoustic phonon mode of ionic liquids consisting of 1-alkyl-3-methyl-imidazolium family (C_nMIM) cations with n values ranging from 2 to 10 and bis(trifluoromethylsulfonyl)amide (TFSA) anion in the temperature range from 300 K to 100 K. [C_nMIM]⁺[TFSA]^? showed depolarized (VH) components of Brillouin peaks at temperatures below the glass transition temperature when n is larger than 4. On the other hand, in the case of ionic liquids with different anions, such as [C₄MIM]⁺[BF₄]^?, [C₄MIM]⁺[PF₆]^? and [C₈MIM]⁺[BF₄]^?, the VH component of Brillouin peaks was not observed in the temperature range investigated. The dielectric loss spectra showed that the temperature dependence of alkyl chain domain relaxation of all ionic liquids followed the Arrhenius law and showed an increase in activation energy at the temperature where the VH component of Brillouin peak appeared. These results suggest that the observed depolarized component of Brillouin peak might originate from uniquely induced polarization in the 2nd domain composed of head groups of cations and anions.