Vibronic state specific predissociation rates from excited electronic states

It is shown that predissociation can be perceived as a primary process due to the continuum part of a Morse oscillator potential. In the model proposed here internal conversion to the ground state is thus not necessarily the primary process of a consecutive dissociation but may be a simultaneous decay. As a consequence, dissociation rates should show strong variations from specific (ro-) vibrational states of the first excited electronic states that are similar to those known from “pure” internal conversion rates. This behaviour is demonstrated by calculating predissociation rates for the process. Especially the out-of-plane modes seem to play an extraordinary role in the excess energy behaviour of the predissociation rate. At lower excess energies, rates from single vibronic levels with out-of-plane mode characteristics may show an increase by several orders of magnitude. Received: 13 November 1998     

Coherent resonant transport through a mesoscopic system with quantum ac microwave field

The time-dependent transport through an ultrasmall quantum dot coupling to two electron reservoirs is investigated. The quantum dot is perturbed by a quantum microwave field (QMF) through gate. The tunneling current formulae are obtained by taking expectation values over coherent state (CS), and SU(1,1) CS. We derive the transport formulae at low temperature by employing the nonequilibrium Green function technique. The currents exhibit coherent behaviors which are strongly associated with the applied QMF. The time-dependent currents appear compound effects of resonant tunneling and time-oscillating evolution. The time-averaged current and differential conductance are calculated, which manifest photon-assisted behaviors. Numerical calculations reveal the similar properties as those in classical microwave field (CMF) perturbed system for the situations concerning CS and squeezed vacuum SU(1,1) CS. But for other squeezed SU(1,1) CS, the tunneling behavior is quite different from the system perturbed by a single CMF through gate. Due to the quantum signal perturbation, the measurable quantities fluctuate fiercely. Received 28 May 1998     

LiAr, LiKr and LiXe excimers: Photochemical formation of the - bands

We investigated the photochemical formation of lithium-rare-gas excimers in the 3 state through the reaction of Li₂(2(C)) and the ground-state rare-gas atom. Lithium-rare-gas vapor mixture was prepared in the heat-pipe oven. We populated the 2(C)state of the Li₂ molecule using the XeCl excimer laser wavelength at 308 nm or the PTP dye laser wavelength at about 335 nm. The 3-1 transitions were observed with peaks at 414, 420 and 435 nm for LiAr, LiKr and LiXe, respectively. We estimated thermally averaged rate constants for these photochemical reactions, which are cm³s^-1 for LiAr, cm ³ s^-1 for LiKr and cm³s^-1 for LiXe. Ab initio potential-energy curves and transition dipole moments for LiKr were calculated applying the SCF MRDCI method. Available data for the LiAr and LiKr excimers are presented, including potential-energy curves, electronic transition dipole moments, and spectroscopic constants. Possible photochemical formation of these molecules in the excited states is discussed. We performed the quantum-mechanical spectral simulations of the LiAr and LiKr 3-1 transitions, using ab initio potential-energy curves. Received: 2 October 1998 / Received in final form: 25 January 1999     

Bias and temperature dependence of the noise in a single electron transistor

Models generalizing the su (2) XX spin-chain were recently introduced. These XXC models also have an underlying su (2) structure. Their construction method is shown to generalize to the chains based on the fundamental representations of the A_m Lie algebras. Integrability of the new models is shown in the context of the quantum inverse scattering method. Their R-matrix is found and shown to yield a representation of the Hecke algebra. The diagonalization of the transfer matrices is carried out using the algebraic Bethe Ansatz. I comment on eventual generalizations and possible links to reaction-diffusion processes. Received: 24 June 1998 / Received in final form: 8 September 1998 / Accepted: 10 September 1998     

Curvature autocorrelations in domain growth dynamics

We show how the interface curvature autocorrelation function (ICAF) and associated structure factor (ICSF), of relevance in non-equilibrium pattern-formation problems where sharp interfaces are present, provide new and interesting information on domain structure, as yet not visible via the order-parameter structure factor (OPSF). This is done by discussing numerical simulations of model A (non-conserved relaxational phase-ordering kinetics) in two-dimensional systems. The ICAF is Gaussian over short distances and exhibits dynamical scaling and t ^1/2 power-law growth. We use it to show what the typical length-scale in the model A dynamics corresponds to physically and how it can be obtained uniquely, rather than simply within a multiplicative constant. Experimental methods to measure the ICAF and/or ICSF are still needed at this point. Received 22 April 1998     

Formation of ordered micro-porous membranes

Regular micro-porous polymeric membranes have recently been discovered by rapidly evaporating a solution of CS₂ containing poly(p-phenylene)-block-polystyrene [#!ref1!#]. 1,2-dichloroethane (a chlorated solvent in which polystyrene gel phase has never been observed) is also found to produce ordered structures, which definitively excludes eventual effect of the gelation process during the membrane formation. The observation of the solution surface during the solvent evaporation reveals the growing of micron-sized water droplets trapped at the surface and forming compact aggregates. The study of the solution/water interface shows that the water droplets profile is in agreement with the pore shape observed in the membranes. Moreover, the copolymer was found to precipitate at the interface, forming a layer encapsulating the droplets and preventing their coalescence. In that way, the final structure results from the droplets stacking under the action of large surface currents. Finally, we argue that the decisive element in the formation of ordered structures is the ability of the polymer to precipitate at the solution/water interface, which seems to be related the star-polymer microstructure. Received: 18 August 1998     

Surface reorientation dynamics of nematic liquid crystals

In this paper we report an experimental investigation on the dynamics of the azimuthal director reorientation at a nematic-solid interface. Three qualitatively different kinds of substrates have been investigated: I) intrinsically anisotropic SiO-substrates (-evaporation), II) isotropic SiO-substrates (-evaporation) and III) rubbed PVA-substrates. In the case II), an in-plane anisotropy was induced cooling slowly the thermotropic nematic liquid crystal (NLC) from the isotropic phase in the presence of a 0.75 T magnetic field. The reorientation dynamic of the surface azimuthal director angle at the switching-on and off of a magnetic (or electric) field has been investigated. All the substrates show comparable azimuthal anchoring energies and two dynamic regimes: a fast dynamic response, driven by the bulk director reorientation and an extremely slow reorientation. The slow dynamics is explained in terms of anisotropic adsorption of NLC molecules on the solid substrate and is well represented by a stretched exponential. Received 7 December 1998     

Dissociative attachment of low-energy electrons to vibrationally excited molecules using a photoelectron source

The process of dissociative attachment (DA) of low-energy electrons ) to vibrationally excited sodium dimer molecules is studied with high electron energy resolution () in a supersonic molecular beam. A novel photoelectron source, based on two-step photoionization of the sodium atoms in the beam, may deliver a current of up to 1 nA and has been used with a current of typically 0.2 nA in this experiment. The energy dependence of the rate of sodium anion formation is determined by ion detection based on a time-of-flight analysis. The molecules are selectively excited to levels using the technique of coherent population transfer by delayed pulses (STIRAP). The comparison of the experimental data with recent resonance model calculations based on improved potential curves reveals generally good agreement for levels v ”>12. For some distinct differences between theoretical and experimental results persist. Received: 21 November 1998 / Received in final form: 7 April 1999     

Magnetic fluctuations in coupled inequivalent Hubbard layers as a model for

We investigate, within the fluctuation-exchange approximation, a correlated-electron model for represented by two inequivalent Hubbard layers coupled by an interlayer hopping . An energy offset is introduced in order to produce a different charge carrier concentration in the two layers. We compare several single-particle and magnetic excitations, namely, the single particle scattering rate, the spectral function and the spin lattice as well as spin-spin relaxation times in the two layers as a function of . We show that the induced interlayer magnetic coupling produces a tendency to “equalization” of the magnetic properties in the two layers whereby antiferromagnetic fluctuations are suppressed in the less doped layer and enhanced in the heavily doped one.The strong antiferromagnetic bilayer coupling causes the charge carriers in the plane with larger doping concentration to behave similar to those of the underdoped layer, they are coupled to. This effect grows for decreasing temperature. For high temperatures or if both layers are optimally or overdoped, i.e. when the antiferromagnetic correlation length becomes of the order or smaller than one lattice site the charge carrier and magnetic dynamics of the two layers is disconnected and the equalization effect disappears. These results are in good agreement with NMR experiments on by Stern et al. [Phys. Rev B 51, 15478 (1995)]. We also compare the results with calculations on bilayer systems with equivalent layers as models for the constituent compounds and . Received: 28 August 1998