Magnetic field effect on the pairing state competition in quasi-one-dimensional organic superconductors (TMTSF)2X

We study the effect of the magnetic field on the pairing state competition in organic conductors (TMTSF)₂X by applying random phase approximation to a quasi-one-dimensional extended Hubbard model. We show that the singlet pairing, triplet pairing and the Fulde–Ferrell–Larkin–Ovchinnikov (FFLO) superconducting states may compete when charge fluctuations coexist with spin fluctuations. This rises a possibility of a consecutive transition from singlet pairing to FFLO state and further to S_z = 1 triplet pairing upon increasing the magnetic field. We also show that the singlet and S_z = 0 triplet components of the gap function in the FFLO state have “d-wave” and “f-wave” forms, respectively, which are strongly mixed.     

Time-reversal symmetry-breaking in two-band superconductors

Competition between an interband Josephson interaction and a biquadratic interband interaction can break time-reversal symmetry when the interband interactions are very weak compared with the intraband interaction. We demonstrate this using the phenomenological Ginzburg–Landau free energy, taking into account terms essential for this phenomenon. This time-reversal symmetry-breaking state peels away a sheet of an interband phase difference soliton wall. This sheet is the domain wall between two different chiral states. The peeling reduces the formation energy of the domain wall. The domain wall can simultaneously erase the Meissner effect and the specific heat jump when the entropy invokes many domain walls, and its life time is prolonged by a pinning owing to an inhomogeneity such as surface roughness.     

Photoluminescence of SrGa2S4:Sn,Re(=Ce, Gd) phosphors

The photoluminescence (PL) spectra, PL excitation spectra, color coordinates, and X-ray diffraction spectra are reported for SrGa₂S₄:Sn,Re(=Ce and Gd, respectively) phosphors. By mixing SrGa₂S₄:Sn,Ce phosphors with different Ce³⁺ concentrations, white emissions can be obtained under the excitation of a 340-nm UV LED. Emissions in the green to yellow color range can be obtained from SrGa₂S₄:Sn,Gd phosphors. The rare earth ions enhance the green emission band, which peaks at 534 nm, instead of the yellow one. The origin of this enhancement is discussed. The resonant energy transfer rates are estimated in the cases from Ce³⁺ to the green and yellow centers of Sn²⁺ and between the yellow centers and the green centers.     

Multifold enhancement of quantum dot luminescence in plasmonic metamaterials

We report that hybridizing semiconductor quantum dots with plasmonic metamaterial leads to a multifold intensity increase and narrowing of their photoluminescence spectrum. The luminescence enhancement is a clear manifestation of the cavity quantum electrodynamics Purcell effect and can be controlled by the metamaterial's design. This observation is an essential step towards understanding loss compensation in plasmonic metamaterials with gain media and for developing metamaterial-enhanced gain media.     

An alternative theorem for set-valued maps via set relations and its application to robustness of feasible sets

Abstract

This paper contains a generalized Gordan-type alternative theorem for set-valued maps which characterizes set relations without any convexity assumptions using certain evaluation functions. As a direct consequence and as a good example, we discuss robustness (or stability) of linear programming problems for modelling error. Moreover, this theorem can be utilized for that of general vector optimization problems in special cases due to reformation of the evaluation functions.     

Global solvability for abstract semilinear evolution equations

The Cauchy problem for the abstract semilinear evolution equation u^′(t) = Au (t) + B (u (t)) + C (u (t)) is discussed in a general Banach space X. Here A is the so‐called Hille‐Yosida operator in X, B is a differentiable operator from D (A) into X, and C is a locally Lipschitz continuous operator from D (A) into itself. A vectorvalued functional defined only on X is used and appropriate conditions on the nonlinear operators B and C are imposed so that a vector‐valued functional defined on the domain of the operator A may be constructed in order to specify the growth of a global solution. The advantage of our formulation lies in the fact that it is possible to obtain a global solution by checking some energy inequalities concerning only low order derivatives (© 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Synthesis of Non-natural Xyloglucans by Polycondensation of 4,6-Dimethoxy-1,3,5-triazin-2-yl Oligosaccharide Monomers Catalyzed by Endo-β-1,4-glucanase

Summary: A cellotetraose-backboned hepta-saccharide (XXXG) (a capital X represents a glucopyranose residue that is substituted with a xylopyranose through an α-1,6 glycosidic bond, and a capital G represents a non-substituted glucopyranose residue) and a nona-saccharide (XLLG) (a capital L represents a glucopyranose residue that is substituted with a galactopyranoseβ(1-2)xylopyranose through an α-1,6 glycosidic bond) have directly been converted to the corresponding 4,6-dimethoxy-1,3,5-triazin-2-yl derivatives (DMT-β-XXXG 1 and DMT-β-XLLG 2 , respectively) by the action of 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methyl morpholinium chloride (DMT-MM). The selective nucleophilic attack of the anomeric hydroxyl group to DMT-MM has been achieved in water without using any protection of the hydroxyl groups. The resulting activated oligosaccharide derivatives ( 1 and 2 ) were found to polymerize catalyzed by an endo-β-1,4-glucanase as catalyst. The polymerization took place in a complete regio- and stereo-selective manner, affording non-natural polysaccharides having a XXXG-repeating unit and a XLLG-repeating unit, respectively, in the main chain. It is extremely difficult to construct such definite repeating structures via the conventional synthetic routes including protection-deprotection procedures.     

Reversible activation of diblock copolymer monolayers at the interface by pH modulation, 2: Membrane interactions at the solid/liquid interface

A monolayer of the pH-responsive poly[2-(dimethylamino)ethyl methacrylate-block-methyl methacrylate] diblock copolymer [PDMAEMA-PMMA] was transferred from the air/water interface to a silicon substrate for evaluation as a tunable interlayer between biological material and solid substrates. Specular neutron reflectivity experiments revealed that the weak polyelectrolyte PDMAEMA chains at the solid/liquid interface can be reversibly activated by pH modulation. The thickness, scattering length density, and surface roughness of the polymer film can be systematically controlled by pH titration. As a simple model of plasma membranes, a lipid bilayer was deposited onto the polymer film. The membrane-substrate interaction was characterized by neutron reflectivity experiments, demonstrating that the membrane-substrate distance could be reversibly regulated by pH titration. These results confirm the potential of stimuli-responsive polymers for precise control of cell-surface interactions.     

Chirality control in oligothiophene through chiral wrapping

[structure: see text] Mixing oligothiophenes and polysaccharides, such as amylose and schizophyllan, affords novel inclusion complexes, in which oligothiophene guests adopt twisted conformation in the chiral channel created by left- or right-handed helical wrapping with the polysaccharide host polymers, leading to optical activity.     

Determination of electron effective mass from optical transition energy in InGaAs/InAlAs quantum wells

Nonparabolic effective mass of conduction subbands in InGaAs/InAlAs quantum wells (QWs), lattice-matched to InP, was quantitatively obtained by analyzing interband-optical transition spectra. Thickness of InGaAs well was 5.3, 9.4, and . Thickness of InAlAs barrier was about , and each QW was independent. Excellent agreement was obtained between experimental mass and theoretical mass predicted by Kane's three-level band theory on bulk InGaAs, in a wide energy range of from the bandedge. Method of experimental analysis on a relation between eigen energy and effective mass was described.