National Institute Of Materials Physics - Romania

We develop a theory of the kinetics of the Bose-Einstein condensation of bosonic excitons interacting with a thermal bath of acoustic phonons. We emphasize several delicate aspects of the condensation kinetics within the framework of rate equations. We give detailed proofs about the existence and uniqueness of the solution with a condensate and illustrate details within exactly or almost exactly solvable models. In particular, we predict an exciton condensation time in Cu2O which is shorter than the lifetime of paraexcitons.

Quasicrystalline icosahedral and amorphous phases prepared as thin films or bulk samples in the systems Al-Pd-Re, Al-Cu-Fe and Ti-Zr-Ni, have been investigated with respect to their temperature dependence of conductance and thermopower, in the range between 10 and 300 K. Various conduction mechanisms yield different exponent values in the power-law temperature dependence of conductance, Tt. A semi-metal behaviour (zeta congruent to 1.5) is found in the amorphous phase and in the disordered icosahedral Al-Pd-Rt: film and Ti-Zr-Ni ribbons, as well as in icosahedral Al-Cu-Fe films. Lower zeta values found in the quasi-perfect icosahedral Al-Pd-Re bulk sample and in two of the icosahedral Al-Cu-Fe films suggest that electron localization in a hierarchy of clusters is the main conduction mechanism in these samples. The thermopower data support the existence of a pseudo-gap at the Fermi level and suggest a similar short-range order in both amorphous and icosahedral phases. The special sensitivity of the thermopower to the DOS details at E-F is responsible for the strong variation of its magnitude with the degree of icosahedral order.

The Ca0.45CU0.55O phase was successfully produced from a mixture of Ca and Cu nitrate powders with cation ratio Ca:Cu = 1:1. The heat treatment for decomposition and the synthesis of the indicated phase were pet-formed at 710 degrees C in air and flowing oxygen, respectively. The Ca0.45Cu0.55O phase concentration increases with synthesis time. After 209 h of heat treatment, the concentration of the Ca0.45Cu0.55O phase determined by X-ray diffraction (XRD) analysis has reached 87% and the kinetic data have indicated that the material enters the saturation stage of the reaction, The secondary phases are CaO and CuO. (C) 2000 Elsevier Science B.V. All rights reserved.

A series of compounds YbxM4Sb12, M = Fe, Co, FeCo, Rh,Ir, were synthesised by reaction sintering. From Rietveld refinements isotypism was determined in all cases with the LaFe4P12-(skutterudite)-type, space group Im (3) over bar - No. 204. These refinements also served to derive the Yb-content in the samples. There is a systematic trend for the Yb-occupancy in the parent lattice M4Sb12; revealing a gradual decrease of the Yb-content from x = 0.8 (M = Fe), x = 0.5 (FeCo), x = 0.2 (Co); x = 0.1 (Rh) to x approximate to 0.02 (Ir). This dependency seems to correlate with the thermal stability of the ternary compounds: a true ternary compound forms for M = Fe, whilst for M = Co, Rh, Ir stable binary skutterudite compounds MSb3 already exist. Measurements of various bulk properties revealed the absence of any long range magnetic order in this series of compounds. While the samples rich in Yb behave metallic like, the Rh and Ir based skutterudites show a semiconducting-like resistivity which at lower temperatures is characterised by variable range hopping in the presence of strong Coulomb interaction. Although Yb0.1Rh4Sb12 exhibits a Seebeck coefficient up to about 150 mu V/K, figures of merit ZT generally are below 0.1 near room temperature, primarily due to the large resistivities of the sintered material.

We calculate the ground state of a two-dimensional electron gas in a shea-period lateral potential in magnetic field, with the Coulomb electron-electron interaction included in the Hartree-Fock approximation. For a sufficiently short period the dominant Coulomb effects are determined by the exchange interaction. We find numerical solutions of the self-consistent equations that have hysteresis properties when the magnetic field is tilted and increased, such that the perpendicular component is always constant. This behavior is a result of the interplay of the exchange interaction with the energy dispersion and the spin splitting. We suggest that hysteresis effects of this type could be observable in magnetotransport and magnetization experiments on quantum-wire and quantum-dot superlattices.

A far-from-equilibrium preparation route and using a particular combination of starting materials led us to obtain nonstoichiometric Y(Fe,V)(12) and its interstitial carbide. Structural analysis and EDAX results reveal the formation of the main 1:12 phase with the ThMn12-type structure, with 13-15% vacancies at the 3d metal sites. Insertion of interstitial carbon increases the T-C and magnetization of the 1:12 phase, whereas the unit cell volume remains unchanged. The effects of vacancies and interstitial carbon on the Mossbauer hyperfine fields and isomer shifts are discussed with reference to the calculated quantities. (C) 2000 Elsevier Science S.A. All rights reserved.

The morphology and structure of a La0.6Y0.07Ca0.33MnO3 thin film is studied by transmission electron microscopy. The film was grown by pulsed laser deposition (PLD) on an MgO-buffered silicon <100> wafer. The as-deposited films are polycrystalline and show a columnar morphology. We present a detailed high-resolution transmission electron microscopy structural study concerning a possible monoclinic distortion of the orthorhombic LYCMO crystal cell. (Received February 22, 2000; accepted March 10, 2000).

Elastic recoil detection analysis (ERDA) has been applied to determine the composition of carbon nitride and hydrogenated carbon nitride films prepared by hollow cathode discharge process. The films were deposited on Si (111) substrates. The films were also characterized by Fourier transform infrared spectroscopy (FTIR). The influence of the main deposition parameters (substrate bias voltage, nitrogen injection mode) on the film properties was investigated. (C) 1000 Elsevier Science B.V. All rights reserved.

Carbon nitride thin films (CNx) were produced by UV laser (ArF, lambda=193 nm) induced chemical vapour deposition from C2H2/NH3 mixtures, on Si and TiN/Si substrates. The surface and bulk composition of the deposited layers were investigated by X-ray photoelectron spectrometry (XPS) and elastic recoil detection analysis (ERDA), respectively. Nitrogen was found to be singly and doubly bonded to carbon, as revealed by FTIR spectrometry. Specific morphology of the films was evidenced by transmission electron microscopy (TEM), while selected area electron diffraction (SAED) confirms the presence of nano-crystallites in the layers. The calculated d-lattice spacings fit rather well with theoretical and experimental data for alpha- and beta-C3N4. (C) 2000 Elsevier Science S.A. All rights reserved.