Predicted effects of gamma and neutron irradiation on silicon solar cells

Numerical analysis of the characteristics of silicon solar cells under-ray or fast neutron irradiation is presented. The degradation of spectral response, short-circuit current, maximum power, open-circuit voltage and curve power factor are discussed. The calculation is based on estimating the minority carrier lifetime by the Shockley-Read equation, assuming the introduction rate, capture cross-section and the energy level to be equal to those of various predominant recombination centres, such as E-centre (phosphorus-vacancy complex), A-centre (oxygen-vacancy complex) and J-centre (boron-vacancy complex) in-irradiated silicon single crystals. The simulated results show good agreement with experiment for N-type F·Z and C·Z bulk crystals with E-centres, and for P-type C·Z bulk crystal with J-centres.     

Theoretical analysis of soil reaction on a lug of the movable lug cage wheel

The measurement of soil reaction forces on a lug of a movable lug cage wheel was carried out in a soil bin. To elucidate the experimental results, a theoretical analysis of soil reaction forces on the lug of the movable lug cage wheel was made by using an analysis of the lug trajectory and a modified theory in soil–vehicle mechanics. The existing theory was modified and adjusted by considering the actual lug trajectory and the soil trench made by the preceding lug. The results showed that the theoretical analysis gave a good representation of the reaction forces measured experimentally. The higher pull and lift forces of the movable lug cage wheel compared with those of the fixed lug wheel was supported by the theoretical analysis. Although the theoretical representation of soil reaction forces should be improved by further works, it is sufficiently accurate to estimate the performance of the movable lug cage wheels by the proposed theory.     

Signal Penetration into Thick Clouds Studied by Multi-Layer Data Observed with a Micro-Pulse Lidar

Lidar return signals are studied for a micro-pulse lidar under sky conditions with multi-layer clouds. From theoretical considerations on the lidar signal-to-noise ratio, it is estimated that the maximum cloud optical thickness detectable is about 3.7. This result reasonably agrees with the actual multi-layer cloud data obtained from observations in Sukhothai, Thailand. Deviations from theoretical prediction, however, are found for a geometrically thin but dense cloud, and for a moderately concentrated but geometrically thick cloud. The effect of multiple scattering is also discussed.     

Lithiosilanes and their application to the synthesis of polysilane dendrimers

An account is given of the preparation and structural investigations of silyllithium compounds, including X-ray and NMR data. This review covers the chemistry of lithiosilanes with alkyl, aryl, functional substituents and lithiooligosilanes with Si---Si bonds. Application of lithiosilanes for the synthesis of polysilane dendritic molecules is also described.     

Predictions of cation and anion effects on solubilities,selectivities and permeabilities for CO2 in ionic liquid using COSMO based activity coefficient model

The solubilities and selectivities for CO₂, N₂ and CH₄ in ionic liquid were predicted using a COSMO based activity coefficient model, COSMO-SAC method. The 1-alkyl-3-methylimidazolium cations were focused in this work. The anion species include tetrafluoroborate [BF₄], hexafluorophosphate [PF₆], triflate [OTf], dicyanamide [dca] and bis(trifluoromethane)-sulfonimide [Tf₂N]. The predicted results of the solubilities of CO₂ in the ionic liquids by COSMO-SAC method are in agreement with the experimental data within the averaged deviation of 0.0017 in mole fraction. The predicted results of selectivities for CO₂/N₂ and CO₂/CH₄ represent the effects of anion species qualitatively. Permeability through supported liquid membrane can be presented by solubility and diffusion coefficients in the liquid. The permeabilities of CO₂ through the ionic liquid membranes were also predicted by a solution-diffusion model with COSMO-SAC method. The predicted results of the CO₂ permeabilities through the ionic liquids represent the experimental data within the order of the permeabilities.     

Self‐Assembly of One‐ and Two‐Dimensional Hemoprotein Systems by Polymerization through Heme–Heme Pocket Interactions

Supramolecular protein polymers : When a heme moiety was introduced to the surface of an apo‐cytochrome b₅₆₂(H63C) mutant, supramolecular polymers formed through noncovalent heme–heme pocket interactions. The incorporation of a heme triad as a pivot molecule in the protein polymer further led to a two‐dimensional protein network structure, which was visualized by tapping‐mode atomic force microscopy (see picture).

     

Investigation of charge transfer and structural distortions during photo-inducted excitation of cuprous bis-2,9-dimethyl-1,10-phenanthroline complex by density functional theory

This work reported the investigation of the structural distortions and charge-transfer processes that occurred in the complex of cuprous(I) bis-2,9-dimethyl-1,10-phenanthroline upon oxidation to copper(II), , through a excited state of by density functional theory. The intramolecular electronic transfer from central metal-to-ligand (MLCT) upon the irradiation of light energy is confirmed. Due to this MLCT excitation, the structure of the excited state of is distorted and reorganized to adapt with the change of charge in central metal. As a result, the excited state of is formed, which has the similar electronic and structural properties with . The bulky substituents in 2- and 9-positions of the phenanthroline ligands can restrain the structural distort and decrease nonradiative decay rate. Thus, the electronic and steric effects of the ligands in the cuprous photo-sensitive complexes have important consequences in the behavior of their excited state.     

Synthesis of bridged nicotinates having [n](2,5)pyridinophane skeletons (n=8-14)

Synthesis of various bridged nicotinates 6 having [n](2,5)pyridinophane skeletons (n=8-14) was accomplished by the unique pyridine-formation reaction of methyl propiolate with a series of formyl-substituted (vinylimino)phosphoranes 5, which were prepared from the corresponding cycloalkanones 1 via Vilsmeier-Haack formylation giving chloro-substituted cycloalkenals 2, their thermal and photochemical transformation to formyl azirines 4, and the following ring-opening reactions with triphenylphosphine. The HPLC analysis of [11](2,5)pyridinophane derivatives, (S_p,S)-14 and (R_p,S)-14, showed that these diastereomers rapidly epimerize themselves at room temperature and that their planar-chirality was thermodynamically less stable as compared to the corresponding [11](2,5)cyclophane systems.