Global solution to a phase transition model based on a microforce balance

Our aim in this article is to prove the existence and the uniqueness of a global solution to a nonisothermal Ginzburg-Landau (Allen-Cahn) system. This system is obtained by considering, in addition to the fundamental laws of thermodynamics, a balance law for internal microforces proposed by M. Gurtin.     

Measurability implies continuity for solutions of functional equations - even with few variables

Summary. We prove that - under certain conditions - measurable solutions $f$ of the functional equation $f(x)=h(x,y,f(g_{1}(x,y)),\ldots,f(g_{n}(x,y))),\quad(x,y)\in D \subset \mathbb{R}^{s} \times \mathbb{R}^{l}$ are continuous, even if $1\le l\le s$. As a tool we introduce new classes of functions which - roughly speaking - interpolate between continuous and Lebesgue measurable functions. Connection between these classes are also investigated.     

Characterization of Cds clusters in zeolite-A grown in alkaline solution

CdS clusters were synthesized in A type zeolite by reaction in alkaline aqueous solution at temperatures from 30 to 70 °C. The optical properties of the samples were studied by diffuse reflectance and photoluminescence spectroscopy. Their crystalline structure and morphology were studied by X-ray diffraction and by transmission and scanning electron microscopy. We found that at lower temperatures the CdS clusters are encapsulated in the zeolite cages. We compared the properties of these clusters with those encapsulated in the cages of zeolites X and Y, prepared by similar methods. CdS clusters smaller than the CdS exciton diameter are also formed outside the cages in the zeolite matrix. The size of these clusters increases with temperature producing a red-shift of the absorption edge in the optical absorption spectra.     

Extremely large binding energy of biexcitons in an organic-inorganic quantum-well material (C4H9NH3)2PbBr4

We have confirmed biexciton formation in an organic-inorganic hybrid quantum-well material (C₄H₉NH₃)₂PbBr₄ by photoluminescence and two-photon absorption measurements. The biexciton has extremely large binding energy, 60 meV, which to our knowledge is the largest value ever reported for a semiconductor. By analyzing the spectrum of biexciton luminescence, the biexciton gas temperature was found to be much higher than the bath temperature due to a higher local temperature arising from the large biexciton binding energy.     

Pressure-induced polymorphism in enstatite (MgSiO3) at room temperature: clinoenstatite and orthoenstatite

The phase transition of a synthetic clinoenstatite in a diamond-anvil cell has been studied by using Raman spectroscopy at various pressures and room temperature. The phenomena observed in clinoenstatite have been compared with that observed in orthoenstatite. It is found that the pressure-induced phase transitions in the two enstatites are reversible, but with different transition pressures and transition behavior. An analysis of Raman spectra has revealed that the two enstatites have different high-pressure polymorphs. This result suggests that the space group of the high-pressure polymorph of orthoenstatite is not of C2/c, and that orthoenstatite and orthoferrosilite have different transition routes at room temperature and high pressure. The compressional behavior of the high-PC2/c enstatite is also discussed according to the pressure dependences of Raman frequencies.     

Investigation of the effect of CdCl2 processing on vacuum deposited CdS/CdTe thin film solar cells by DLTS

Thin film CdS/CdTe solar cells have been prepared by conventional vacuum deposition technique. Deep level transient spectroscopy (DLTS), temperature and frequency dependent capacitance-voltage (C-V) measurements were utilised to investigate the performance limiting defect states in the CdTe layer subjected to the post deposition treatments such as CdCl₂-dipping and/or annealing in air. Five hole traps, all of which have been previously reported in the literature, were identified in as-grown CdTe at 0.19, 0.20, 0.22, 0.30 and 0.40 eV above the valence band. A single hole trap level has been evidenced at 0.45 eV after both post deposition heat and CdCl₂ treatments.     

Zero-divisor graphs, von Neumann regular rings, and Boolean algebras

For a commutative ring R with set of zero-divisors Z(R), the zero-divisor graph of R is Γ(R)=Z(R)−{0}, with distinct vertices x and y adjacent if and only if xy=0. In this paper, we show that Γ(T(R)) and Γ(R) are isomorphic as graphs, where T(R) is the total quotient ring of R, and that Γ(R) is uniquely complemented if and only if either T(R) is von Neumann regular or Γ(R) is a star graph. We also investigate which cardinal numbers can arise as orders of equivalence classes (related to annihilator conditions) in a von Neumann regular ring.     

The convergence rate of continued fractions representing solutions of a Riccati equation

The aim of this note is to generalize and apply results on matrix continued fractions representing the solution of discrete matrix Riccati equations. Assuming uniform bounds for the norm of the matrix coefficients of the continued fraction, the minimal and maximal solutions of the corresponding algebraic Riccati equation can be accurately enclosed.     

Degree bounds for syzygies of invariants

Suppose that G is a linearly reductive group. Good degree bounds for generators of invariant rings were given in (Proc. Amer. Math. Soc. 129 (4) (2001) 955). Here we study minimal free resolutions of invariant rings. For finite linearly reductive groups G it was recently shown in (Adv. Math. 156 (1) (2000) 23, Electron Res. Announc. Amer. Math. Soc. 7 (2001) 5, Adv. Math. 172 (2002) 151) that rings of invariants are generated in degree at most the group order |G|. In characteristic 0 this degree bound is a classical result by Emmy Noether (see Math. Ann. 77 (1916) 89). Given an invariant ring of a finite linearly reductive group G, we prove that the ideal of relations of a minimal set of generators is generated in degree at most ?2|G|.     

α-Fe2O3-In2O3 mixed oxide nanoparticles synthesized under hydrothermal supercritical conditions

α-Fe₂O₃-In₂O₃ mixed oxide nanoparticles system has been synthesized by hydrothermal supercritical and postannealing route, starting with (1−x)Fe(NO₃)₃·9H₂O·xIn(NO₃)₃·5H₂O aqueous solution (x=0-1). X-ray diffraction and Mössbauer spectroscopy have been used to study the phase structure and substitutions in the nanosized samples. The concentration regions for the existence of the solid solutions in the α-Fe₂O₃-In₂O₃ nanoparticle system together with the solubility limits of In³⁺ ions in the hematite lattice and of Fe³⁺ ions in the cubic In₂O₃ structure have been evidenced. In general, the substitution level is considerably lower than the nominal concentration x. A justification of the processes leading to the formation of iron and indium phases in the investigated supercritical hydrothermal system has been given.