Preparation of silicate tungsten bronzes on aluminum by plasma electrolytic oxidation process in 12-tungstosilicic acid

The growth of silicate tungsten bronzes on aluminum by plasma electrolytic oxidation in 12-tungstosilicic acid is experimentally investigated and discussed. Real time imaging and optical emission spectroscopy characterization of plasma electrolytic oxidation show that spatial density of microdischarges is the highest in the early stage of the process, while the percentage of oxide coating area covered by active discharge sites decreases slowly with time. Emission spectrum of microdischarges has several intensive band peaks originating either from aluminum electrode or from the electrolyte. Surface roughness of obtained oxide coatings increases with prolonged time of plasma electrolytic oxidation, as their microhardness decreases. Raman spectroscopy and energy dispersive X-ray spectroscopy are employed to confirm that the outer layer of oxide coatings formed during the plasma electrolytic oxidation process is silicate tungsten bronzes.     

Depletion of arginine in yeast cells decreases the resistance to hydrostatic pressure

High hydrostatic pressure (HP) inhibits growth and inactivates microorganisms by destabilizing non-covalent molecular interactions. Arginine contributes to stress resistance because it has a guanidine side chain, which assists in the refolding of aggregated proteins. We attempted to analyze the contribution of arginine to high HP stress using a pressure-sensitive mutant strain of Saccharomyces cerevisiae and a metabolomics approach. Our results showed that the content of 136 out of 250 detected metabolites differed in the mutant and parent strains. Decreased metabolites were involved in the tricarboxylic acid cycle and arginine biosynthesis. The expression of genes contributing to arginine biosynthesis was significantly lower in the mutant strain than in the parent strain. When arginine was supplemented to the medium, the mutant strain showed more tolerance to pressure. These results suggest that yeast cells survived due to the contribution of arginine to high pressure resistance. This indicates that depletion of arginine caused by decreased activity of the biosynthesis pathway confers sensitivity to HP.     

Frequency-doubling of an optical vortex output from a stressed Yb-doped fiber amplifier

The frequency-doubling of a picosecond vortex fiber laser, formed of a 1-μm picosecond master laser and a large-mode-area fiber amplifier by using a nonlinear LiB₃O₅, crystal, was performed. A maximum second-harmonic power of 7.7 W was achieved, corresponding to a conversion efficiency of 31 %. The second harmonic had an annular spatial form owing to a phase singularity with a doubled topological charge, and its wavefront helicity was selectively controlled by tuning the stress applied to the fiber amplifier.     

High-efficiency electro-optic amplitude modulation with delayed coherent addition

Amplitude modulation of laser light is required for resonant sideband extraction employed in gravitational-wave detectors. Amplitude modulation with electro-optic phase modulators is realized by interferometric phase-to-amplitude conversion. Although two outputs modulated at opposite phases to each other are obtained, usually only one of them is utilized and the other is abandoned. The reuse of this abandoned light improves the power efficiency of the modulation. This can be realized by inverting the modulation phase of one output with a delay line and adding it to the other coherently. Moreover, this system selects a high-efficiency operating point and modulates the light in a linear range. We demonstrate that the modulation system can be operated with a power loss that is due only to the losses of the optical components.     

Anion configuration at the air/liquid interface of ionic liquid [bmim]OTf studied by sum-frequency generation spectroscopy

The air/liquid interface of a room temperature ionic liquid, 1-butyl-3-methylimidazolium trifluoromethanesulfonate ([bmim]OTf), is investigated using infrared-visible sum frequency generation (SFG) spectroscopy. The SFG spectra clearly show low-frequency modes [CF 3-symmetric stretching (ss) mode and SO 3-symmetric stretching (ss) mode] of the OTf anion, demonstrating the existence of anions polar oriented at the interface. The amplitude of the CF 3-ss peak of the OTf anion has the opposite sign with respect to that of the SO 3-ss peak, indicating that OTf anions at the surface have polar ordering where the nonpolar CF 3 group points away from the bulk into the air, whereas the SO 3 group points toward the bulk liquid. The line width of the SFG peak from the submerged SO 3 group is appreciably narrower than that from IR absorption, suggesting the environment of the surface OTf anions is much more homogeneous than that of the bulk. The vibrational calculations also suggest that the anions and the cations form a more specific aggregated configuration at the surface as compared to the bulk.     

Synthesis,Structural Characterization,and Optical Properties of Benzene-Fused Tetracyclic and Pentacyclic Stiboles

The expectation that antimony (Sb) compounds should display phosphorescence emissions based on the “heavy element effect” prompted our interest in the introduction of antimony to a biaryl as the bridging atom in a fused heterole system. Herein, the synthesis, molecular structures, and optical properties of novel benzene-fused heteroacenes containing antimony or arsenic atoms are described. The stiboles and arsole were prepared by the condensation of dibromo(phenyl)stibane or dichloro(phenyl)arsine with dilithium intermediates derived from the corresponding dibromo compounds. Nuclear magnetic resonance (NMR) spectroscopy and X-ray crystal analysis revealed that the linear pentacyclic stibole was highly symmetric in both the solution and crystal states. In contrast, the curved pentacyclic stibole adopted a helical structure in solution, and surprisingly, only M helical molecules were crystallized from the racemate. All synthesized compounds produced very weak or no emissions at room temperature or in the solid state. In contrast, the linear penta- and tetracyclic stiboles exhibited clear phosphorescence emissions in the CHCl₃ frozen matrix at 77 K under aerobic conditions.     

Oxygen Evolution Catalyzed by a Mononuclear Ruthenium Complex Bearing Pendant SO3− Groups

Rational molecular design of catalytic systems capable of smooth O? O bond formation is critical to the development of efficient catalysts for water oxidation. A new ruthenium complex was developed, which bears pendant SO₃^? groups in the secondary coordination sphere: [Ru(terpy)(bpyms)(OH₂)] (terpy=2,2′:6′,2′′‐terpyridine, bpyms=2,2′‐bipyridine‐5,5′‐bis(methanesulfonate)). Water oxidation driven by a Ce⁴⁺ oxidant is distinctly accelerated upon introduction of the pendant SO₃^? groups in comparisons to the parent catalyst, [Ru(terpy)(bpy)(OH₂)]²⁺ (bpy=2,2′‐bipyridine). Spectroscopic, electrochemical, and crystallographic investigations concluded that the pendant SO₃^? groups promote the formation of an O? O bond via the secondary coordination sphere on the catalyst, whereas the influence of the pendant SO₃^? groups on the electronic structure of the [Ru(terpy)(bpy)(OH₂)]²⁺ core is negligible. The results of this work indicate that modification of the secondary coordination sphere is a valuable strategy for the design of water oxidation catalysts.     

Redox-responsive conformational alteration of aromatic amides bearing N-quinonyl system

Redox-induced conformational alteration of N-aryl-N-phenylamides, in which the N-aryl group consists of a hydroquinone–p-quinone system, was examined. The reduced form bearing a dihydroxyphenyl or dimethoxyphenyl group exists mainly in the E-form, whereas the oxidized form bearing a N-benzoquinone moiety takes the Z-form both in the crystal and in solution. This redox-induced conformational alteration is associated with a marked change in optical properties. This system appears to have suitable properties for use in external redox stimulus-responsive functional switching.     

Nucleation and grain growth in as deposited and ion implanted GeTe thin films

The crystallization dynamic of amorphous GeTe 50 nm thick films deposited on a SiO₂/Si substrate by RF magnetron sputtering, either ion implanted by Ge⁺ ions or not, has been analyzed in situ by optical microscopy during annealing in the 143-155 °C temperature range. Raman spectroscopy has been also performed in as deposited, ion implanted (i.i.) and melt quenched (m.q.) amorphous samples to compare the local order among the different amorphous structure. Nucleation and growth rates, for i.i. and as deposited samples, have been observed and directly compared by optical microscopy in a region of about 5 × 10⁴ μm². From these data, the activation energy and pre-exponential terms of each process have been calculated. The nucleation rate and growth velocity of the i.i. films increased by a factor thirteen and a factor three with respect to the as deposited samples. This evidence, in agreement with Raman spectroscopy data, suggests that implantation, providing kinetic energy by collision cascade, induces a local atomic rearrangement towards more relaxed amorphous states. As a result the crystallization kinetic is enhanced by the reduction of wrong bonds formed during sputter deposition, a process which occurs far from equilibrium conditions.