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Disordered quantum systems

Thermal Fluctuations in One-Dimensional Disordered Quantum Systems... [Pg.91]

The quantum Langevin equation formalism described here could be also employed for studying the conductance properties of disordered harmonic systems or chains combining impurities. In such systems, mode localization becomes a crucial factor [5,18]. [Pg.278]

DISORDER EFFECTS AND ENERGY RELAXATION IN QUANTUM SYSTEMS ONE-DIMENSIONAL FRENKEL EXCITONS IN MOLECULAR AGGREGATES... [Pg.429]

Disorder effects and energy relaxation in quantum systems One-dimensional Frenkel excitons in molecular aggregates 429... [Pg.531]

The goal of this monograph is to summarize the different quantum-mechanical methods developed in the last 20 years to treat the electronic structure of polymers. Owing to the nature of the problem, these methods consist of a mixture of quantum-chemical and solid-state physical techniques. The theory described in Part I treats, besides the Hartree-Fock problem, the electron correlation, and it has also been developed for disordered polymeric systems. Though for obAdous reasons the book could not include all the existing calculations, each new method described is illustrated by a few applications, with a discussion of the numerical results obtained. For more details see the Introduction to Part I. [Pg.421]

The question of non-classical manifestations is particularly important in view of the chaos that we have seen is present in the classical dynamics of a multimode system, such as a polyatomic molecule, with more than one resonance coupling. Chaotic classical dynamics is expected to introduce its own peculiarities into quantum spectra [29, 77]. In Fl20, we noted that chaotic regions of phase space are readily seen in the classical dynamics corresponding to the spectroscopic Flamiltonian. Flow important are the effects of chaos in the observed spectrum, and in the wavefiinctions of tire molecule In FI2O, there were some states whose wavefiinctions appeared very disordered, in the region of the... [Pg.76]

Unlike the solid state, the liquid state cannot be characterized by a static description. In a liquid, bonds break and refomi continuously as a fiinction of time. The quantum states in the liquid are similar to those in amorphous solids in the sense that the system is also disordered. The liquid state can be quantified only by considering some ensemble averaging and using statistical measures. For example, consider an elemental liquid. Just as for amorphous solids, one can ask what is the distribution of atoms at a given distance from a reference atom on average, i.e. the radial distribution function or the pair correlation function can also be defined for a liquid. In scattering experiments on liquids, a structure factor is measured. The radial distribution fiinction, g r), is related to the stnicture factor, S q), by... [Pg.132]

In photoluminescence one measures physical and chemical properties of materials by using photons to induce excited electronic states in the material system and analyzing the optical emission as these states relax. Typically, light is directed onto the sample for excitation, and the emitted luminescence is collected by a lens and passed through an optical spectrometer onto a photodetector. The spectral distribution and time dependence of the emission are related to electronic transition probabilities within the sample, and can be used to provide qualitative and, sometimes, quantitative information about chemical composition, structure (bonding, disorder, interfaces, quantum wells), impurities, kinetic processes, and energy transfer. [Pg.29]

In this section we review several studies of phase transitions in adsorbed layers. Phase transitions in adsorbed (2D) fluids and in adsorbed layers of molecules are studied with a combination of path integral Monte Carlo, Gibbs ensemble Monte Carlo (GEMC), and finite size scaling techniques. Phase diagrams of fluids with internal quantum states are analyzed. Adsorbed layers of H2 molecules at a full monolayer coverage in the /3 X /3 structure have a higher transition temperature to the disordered phase compared to the system with the heavier D2 molecules this effect is... [Pg.97]

This model, which is sometimes referred to as the Fluctuating Gap Model (FGM) [42], has been used to study various aspects of quasi-one-dimensional systems. Examples arc the thermodynamic properties of quasi-one-dimensional organic compounds (NMP-TCNQ, TTF-TCNQ) [271, the effect of disorder on the Peierls transition [43, 44, and the effect of quantum lattice fluctuations on the optical spectrum of Peierls materials [41, 45, 46]. [Pg.364]

The third law of thermodynamics states that the entropy of a perfect crystal is zero at a temperature of absolute zero. Although this law appears to have limited use for polymer scientists, it is the basis for our understanding of temperature. At absolute zero (-273.14 °C = 0 K), there is no disorder or molecular movement in a perfect crystal. One caveat must be introduced for the purist - there is atomic movement at absolute zero due to vibrational motion across the bonds - a situation mandated by quantum mechanical laws. Any disorder creates a temperature higher than absolute zero in the system under consideration. This is why absolute zero is so hard to reach experimentally ... [Pg.69]


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See also in sourсe #XX -- [ Pg.92 ]




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