Buckling-driven morphological transformation of droplets of a mixed colloidal suspension during evaporation-induced self-assembly by spray drying

Morphological transformation during evaporation-induced self-assembly of a mixed colloidal suspension in micrometric droplets has been investigated. It has been demonstrated that a buckling-driven shape transition of drying droplets of mixed colloidal suspension takes place during evaporation-induced self-assembly. Further, it is also shown that the distortion modulations get significantly amplified with enhancement in volume fraction of anisotropic soft colloidal component of the mixed colloids. It has been argued that the reduction in elastic modulus of formed shell, at the boundary of a drying droplet, and the anisotropic nature of one of the colloidal components facilitate the deformation process. Hierarchical structures of these assembled colloidal grains have been probed using electron microscopy and scattering techniques.     

Electronic structure and magnetism of disordered bcc Fe alloys

We study the electronic structure and magnetic properties of disordered bcc Co_xFe_1-x, Cr_xFe_1-x and Mn_xFe_1-x alloys in their ferromagnetic phases using the Augmented Space Recursion (ASR) technique coupled with the tight-binding linearized muffin tin orbital (TB-LMTO) method. We calculate the density of states and magnetic moment of these alloys to show the variation upon alloying Fe with the other neighbouring 3d transition metals using arguments based on charge transfer, exchange splitting and hybridization effects. Received 10 April 2001 and Received in final form 15 August 2001     

Growth and characterization of Cd1−xZnxTe thin films prepared from elemental multilayer deposition

Cd_1−xZn_xTe is a key material for fabrication of high-energy radiation detectors and optical devices. Conventionally it is fabricated using single crystal growth techniques. The method adopted here is the deposition of elemental multilayer followed by thermal annealing in vacuum. The multilayer structure was annealed at different temperatures using one to five repetitions of Cd-Zn-Te sequence. X-ray diffraction pattern for the multilayer with five repetitions revealed that annealing at 475 °C yielded single-phase material compared to other annealing conditions. EDX spectroscopy was carried out to study the corresponding compositions. Photoluminescence properties and change of resistance of the multilayer under illumination were also studied. The resistivity of the best sample was found to be a few hundreds of Ω cm.     

Room-temperature fluorescence of a charge-transfer complex of reserpine in aqueous and aqueous–ethanol media

The room-temperature fluorescence of a charge-transfer (CT) complex different from those of the component donor/acceptor in polar organic solvent is not very common. The phenomenon is even rarer in aqueous medium. The present work demonstrates that a CT complex formed between reserpine (Res) and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) in aqueous and aqueous–ethanol media exhibits fluorescence at room temperature that is entirely different from those of the components, Res and DDQ. With decreasing polarity of the medium on the addition of ethanol, the fluorescence intensity and also the fluorimetrically determined formation constant of the complex increase, but the fluorescence emission wavelength does not change significantly. The quantum yield of fluorescence of the CT complex systematically decreases with increasing ethanol content of the medium. That the observed fluorescence is due to the CT complex is established by the constancy of the assumed proportionality constant (β) between the fluorescence intensity and the complex concentration measured using different equilibrium concentrations of the complex and also by demonstrating the mirror image relationship between its excitation and emission spectra in aqueous medium. To our knowledge, this is the first report on the room-temperature fluorescence of a CT complex in aqueous solution.     

Effect of hydrogen bond formation on the NMR properties of microhydrated ortho-aminobenzoic acid

The in?uence of the hydrogen bond formation on the nuclear magnetic resonance parameters has been investigated in the case of microhydrated ortho-aminobenzoic acid (o-Abz) in the gas-phase. DFT-B3LYP/aug-cc-pVDZ predicted ¹H and ¹³C isotropic chemical shifts with respect to TMS of the isolated o-Abz are in reasonable agreement with available experimental data. The isotropic and anisotropic chemical shifts for all atoms of o-Abz within the o-Abz?···?(H₂O)_1-3 complexes have been calculated at the Hartree–Fock, and density functional (B3LYP) theoretical levels using the 6-31++G(2d,2p) and aug-cc-pVDZ basis sets and considering the counterpoise corrections for the basis set superposition errors. The chemical shift values of the carboxyl group atoms of microhydrated o-Abz relative to isolated o-abz do not show significant basis set dependence. Both the hydrogen and carbon atoms constituting the carboxyl group of o-Abz suffer downfield shift due to formation of hydrogen bond with water. The length of hydrogen bond formed between o-Abz and water is found to vary with the number of water molecules present around o-Abz. A direct correlation between the hydrogen bond length and isotropic chemical shift of the bridging hydrogen is observed for both C?=?O?···?H-O and O-H?···?O interactions.     

Model-independent calculation of radiative neutron capture on lithium-7

The radiative neutron capture on lithium-7 is calculated model independently using a low-energy halo effective field theory. The cross section is expressed in terms of scattering parameters directly related to the S-matrix elements. It depends on the poorly known p-wave effective range parameter r(1). This constitutes the largest uncertainty in traditional model calculations. It is explicitly demonstrated by comparing with potential model calculations. A single parameter fit describes the low-energy data extremely well and yields r(1)≈-1.47 fm(-1).     

Hall effects on steady hydromagnetic flow in a rotating channel in the presence of an inclined magnetic field

Effects of Hall current on a steady hydromagnetic (MHD) fully developed flow in a rotating environment within a parallel plate channel in the presence of an inclined magnetic field is studied. From an extension of literature [13] subject to a forced oscillation it is observed that the present paper is methodically more correct to work first in the steady state where forced oscillation becomes insignificant and then new results are expected for an unsteady MHD flow under the influence of a pulse-oscillator. Exact solutions of the governing equations are obtained in a closed form. The graphical representation for the velocity and the induced magnetic field are depicted graphically and the heat transfer at both the plates are presented in tables.     

Charge-response of magnetization in nanoporous Pd-Ni alloys

This work reports isothermal reversible variation of magnetization in nanoporous Pd-Ni alloys subjected to continuous charging and discharging of the sample in aprotic electrolyte medium. Polarizing metal surface with excess charge also finds strain in the nanoporous structure using the sample as working electrode. Therefore, it is proposed that pressure induced by strain is the key parameter for the observed reversible magnetization in the transition metal alloys.