Photoluminescence enhancement by localized surface plasmons in AlGaN/GaN/AlGaN double heterostructures

Double heterostructures AlGaN/GaN/AlGaN grown by hydride vapor phase epitaxy and designed for use as light emitting diodes for 360 nm wavelength were patterned by shallow nanoholes and injected with Ag/SiO₂ or Al nanoparticles. A 1.8 times increase in the photoluminescence and microcathodoluminescence signal from the GaN active region was observed for 100 nm diameter Al nanoparticles, the efficiency decreased compared to the reference planar samples for small Al nanoparticles of 30–40 nm diameter, and a moderate increase of 1.2 times was detected for Ag/SiO₂ nanoparticles. The observed phenomena are explained by the GaN emitter coupling with localized surface plasmons produced by metallic nanoparticles. (© 2015 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim)     

Complexation of linear and poly(ethylene oxide)‐grafted poly(methacryl oxyethyl trimethylammonium chloride) with poly(ethylene oxide‐block‐sodium methacrylate)

The interactions between oppositely charged polyelectrolytes were studied in saline aqueous solutions as functions of the temperature and the salt and polymer concentrations. The polyanion was a diblock copolymer composed of a poly(ethylene oxide) block and a poly(sodium methacrylate) block. Two polycations were used, the homopolymer poly(methacryl oxyethyl trimethylammonium chloride) and its poly(ethylene oxide)‐grafted analogue. By dynamic light scattering and turbidity measurements, it was observed that the salt concentration, temperature, and counterion size had a significant effect on the formation of the polymer complexes in aqueous solutions. At a fixed salt concentration and a fixed temperature, it was possible to form completely soluble complexes of an ionic polymer in aqueous solutions between poly(ethylene oxide)‐grafted poly(methacryl oxyethyl trimethylammonium chloride)and the polyanion with a poly(ethylene oxide) block at a 1:1 anion/cation ratio. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 1904–1914, 2003     

More electron rich than cyclopentadienyl: 1,2-diaza-3,5-diborolyl as a ligand in ferrocene and ruthenocene analogs

Ruthenium and iron sandwich complexes incorporating cyclopentadienyl analogs with CB(2)N(2)(-) skeletons were characterized. Electrochemical measurements supported by computational studies revealed that in combination with larger metal ions such as Ru the CB(2)N(2)(-) ligand can be more electron-rich than its organic counterpart.     

Single freezing and triple melting of micrometre-scaled (NH4)2SO4/H2O droplets

Atmospheric aerosol droplets containing NH(4)(+) and SO(4)(2-) ions are precursors of cirrus ice clouds. However, the low-temperature phase transformation of such droplets is not understood yet. Here we show for the first time that micrometre-scaled (NH(4))(2)SO(4)/H(2)O droplets produce one freezing event but three melting events which are the melting of (i) pure ice, (ii) eutectic ice/(NH(4))(2)SO(4), and (iii) eutectic ice/(NH(4))(3)H(SO(4))(2). We also find that the melting of ice/(NH(4))(3)H(SO(4))(2) consists of two eutectic melting events, presumably ice/letovicite-II and ice/letovicite-III.     

Comparisons of relative BV-capacities and Sobolev capacity in metric spaces

We study relations between the variational Sobolev 1-capacity and versions of variational BV-capacity in a complete metric space equipped with a doubling measure and supporting a weak (1,1)-Poincaré inequality. We prove the equality of 1-modulus and the continuous 1-capacity, extending the known results for 1<p<∞ to also cover the more geometric case p=1. Then we give alternative definitions for variational BV-capacities and obtain equivalence results between them. Finally we study relations between total 1-capacity and versions of BV-capacity.     

Bond stretching and redox behavior in coinage metal complexes of the dichalcogenide dianions [(SPh2P)2CEEC(PPh2S)2]2- (E=S, Se): diradical character of the dinuclear copper(I) complex (E=S)

The metathetical reactions of a) [Li(tmeda)]₂[(S)C(PPh₂S)₂] (Li₂? 3 c ) with CuCl₂ and b) [Li(tmeda)]₂[(SPh₂P)₂CSSC(PPh₂S)₂] (Li₂? 4 c ) with two equivalents of CuCl both afford the binuclear Cu^I complex {Cu₂[(SPh₂P)₂CSSC(PPh₂S)₂]} ( 5 c ). The elongated (C)S? S(C) bond (ca. 2.54 and 2.72 Å) of the dianionic ligand observed in the solid‐state structure of 5 c indicate the presence of diradical character as supported by theoretical analyses. The treatment of [Li(tmeda)]₂[(SPh₂P)₂CSeSeC(PPh₂S)₂] (Li₂? 4 b ) and Li₂? 4 c with AgOSO₂CF₃ produce the analogous Ag^I derivatives, {Ag₂[(SPh₂P)₂CEEC(PPh₂S)₂]} ( 6 b , E=Se; 6 c , E=S), respectively. The diselenide complex 6 b exhibits notably weaker Ag? Se(C) bonds than the corresponding contacts in the Cu^I congeners, and the ³¹P NMR data suggest a possible isomerization in solution. In contrast to the metathesis observed for Cu^I and Ag^I reagents, the reactions of Li₂? 4 b and Li₂? 4 c with Au(CO)Cl involve a redox process in which the dimeric dichalcogenide ligands are reduced to the corresponding monomeric dianions, [(E)C(PPh₂S)₂]^2? ( 3 b , E=Se; 3 c , E=S), and one of the gold centers is oxidized to generate the mixed‐valent Au^I/Au^III complexes, {Au[(E)C(PPh₂S)₂]}₂ ( 7 b , E=Se; 7 c , E=S), with relatively strong aurophilic Au^I???Au^III interactions. The new compounds 5 c , 6 b , c and 7 b , c are characterized in solution by NMR spectroscopy and in the solid state by X‐ray crystallography ( 5 c , 6 b , 7 b and 7 c ) and by Raman spectroscopy ( 5 c and 6 c ). The UV‐visible spectra of coinage metal complexes of the type 5 , 6 and 7 are discussed in the light of results from theoretical analyses using time‐dependent density functional theory.     

Fractional Lévy Processes as a Result of Compact Interval Integral Transformation

Fractional Brownian motion can be represented as an integral of a deterministic kernel w.r.t. an ordinary Brownian motion either on infinite or compact interval. In previous literature fractional Lévy processes are defined by integrating the infinite interval kernel w.r.t. a general Lévy process. In this article we define fractional Lévy processes using the com pact interval representation.

We prove that the fractional Lévy processes presented via different integral transformations have the same finite dimensional distributions if and only if they are fractional Brownian motions. Also, we present relations between different fractional Lévy processes and analyze the properties of such processes. A financial example is introduced as well.     

On spaces which are linearly D

We introduce a generalization of D-spaces, which we call linearly D-spaces. The following results are obtained for a T₁-space X.

– X is linearly Lindelöf if, and only if, X is a linearly D-space of countable extent.

– X is linearly D provided that X is submetaLindelöf.

– X is linearly D provided that X is the union of finitely many linearly D-subspaces.

– X is compact provided that X is countably compact and X is the union of countably many linearly D-subspaces.

Distributed termination on a ring

The termination detection problem of a distributed computation has gained considerable interest recently. In this paper two symmetric solutions to this problem are presented in the special case, where the distributed computation is performed by a ring of processes. We shall discuss the problem in terms of processes communicating via shared variables instead of messages.