609 research outputs found
Large magnetoresistance at room-temperature in small molecular weight organic semiconductor sandwich devices
We present an extensive study of a large, room temperature negative
magnetoresistance (MR) effect in tris-(8-hydroxyquinoline) aluminum sandwich
devices in weak magnetic fields. The effect is similar to that previously
discovered in polymer devices. We characterize this effect and discuss its
dependence on field direction, voltage, temperature, film thickness, and
electrode materials. The MR effect reaches almost 10% at fields of
approximately 10 mT at room temperature. The effect shows only a weak
temperature dependence and is independent of the sign and direction of the
magnetic field. Measuring the devices' current-voltage characteristics, we find
that the current depends on the voltage through a power-law. We find that the
magnetic field changes the prefactor of the power-law, whereas the exponent
remains unaffected. We also studied the effect of the magnetic field on the
electroluminescence (MEL) of the devices and analyze the relationship between
MR and MEL. We find that the largest part of MEL is simply a consequence of a
change in device current caused by the MR effect.Comment: 8 figure
Reconfigurable Autonomy
This position paper describes ongoing work at the Universities of Liverpool, Sheffield and Surrey in the UK on developing hybrid agent architectures for controlling autonomous systems, and specifically for ensuring that agent-controlled dynamic reconfiguration is viable. The work outlined here forms part of the Reconfigurable Autonomy research project
Theory of Exciton Migration and Field-Induced Dissociation in Conjugated Polymers
The interplay of migration, recombination, and dissociation of excitons in
disordered media is studied theoretically in the low temperature regime. An
exact expression for the photoluminescence spectrum is obtained. The theory is
applied to describe the electric field-induced photoluminescence-quenching
experiments by Kersting et al. [Phys. Rev. Lett. 73, 1440 (1994)] and Deussen
et al. [Synth. Met. 73, 123 (1995)] on conjugated polymer systems. Good
agreement with experiment is obtained using an on-chain dissociation mechanism,
which implies a separation of the electron-hole pair along the polymer chain.Comment: 4 pages, RevTeX, 2 Postscript figure
Temperature and Field Dependence of the Mobility in Liquid-Crystalline Conjugated Polymer Films
The transport properties of organic light-emitting diodes in which the
emissive layer is composed of conjugated polymers in the liquid-crystalline
phase have been investigated. We have performed simulations of the current
transient response to an illumination pulse via the Monte Carlo approach, and
from the transit times we have extracted the mobility of the charge carriers as
a function of both the electric field and the temperature. The transport
properties of such films are different from their disordered counterparts, with
charge carrier mobilities exhibiting only a weak dependence on both the
electric field and temperature. We show that for spatially ordered polymer
films, this weak dependence arises for thermal energy being comparable to the
energetic disorder, due to the combined effect of the electrostatic and thermal
energies. The inclusion of spatial disorder, on the other hand, does not alter
the qualitative behaviour of the mobility, but results in decreasing its
absolute value.Comment: 9 pages, 8 figures, submitted to Phys. Rev.
Ab-initio calculation of the electronic and optical excitations in polythiophene: effects of intra- and interchain screening
We present an calculation of the electronic and optical excitations of an
isolated polythiophene chain as well as of bulk polythiophene. We use the GW
approximation for the electronic self-energy and include excitonic effects by
solving the electron-hole Bethe-Salpeter equation. The inclusion of interchain
screening in the case of bulk polythiophene drastically reduces both the
quasi-particle band gap and the exciton binding energies, but the optical gap
is hardly affected. This finding is relevant for conjugated polymers in
general.Comment: 4 pages, 1 figur
Theoretical study of electric field-dependent polaron-type mobility in conjugated polymers
We have used a self-consistent quantum molecular dynamics approach to calculate the mobility of both positive and negative polaron-type carriers on solated chains of poly(p-phenylene vinylene) (PPV) and some of its derivatives and the dependence of their mobility on the applied electric field. Our results suggest that polaron-type mobility along most of these polymer chains has a clear dependence on the electric field which is quite different from the result derived for bulk PPV-based materials.Fundação para a Ciência e a Tecnologia (FCT)
Programa Operacional “Ciência , Tecnologia, Inovação” – POCTI/CTM/41574/2001, CONC-REEQ/443/EEI/2001 e SFRH/BD/11231/200
Theory of Electric Field-Induced Photoluminescence Quenching in Disordered Molecular Solids
The dynamics of excitons in disordered molecular solids is studied
theoretically, taking into account migration between different sites,
recombination, and dissociation into free charge carriers in the presence of an
electric field. The theory is applied to interpret the results of electric
field-induced photoluminescence (PL) quenching experiments on molecularly doped
polymers by Deussen et al. [Chem. Phys. 207, 147 (1996)]. Using an
intermolecular dissociation mechanism, the dependence of the PL quenching on
the electric field strength and the dopant concentration, and the time
evolution of the transient PL quenching can be well described. The results
constitute additional proof of the distinct exciton dissociation mechanisms in
conjugated polymer blends and molecularly doped polymers.Comment: 4 pages RevTeX, 3 Postscript figure
Excitons in quasi-one dimensional organics: Strong correlation approximation
An exciton theory for quasi-one dimensional organic materials is developed in
the framework of the Su-Schrieffer-Heeger Hamiltonian augmented by short range
extended Hubbard interactions. Within a strong electron-electron correlation
approximation, the exciton properties are extensively studied. Using scattering
theory, we analytically obtain the exciton energy and wavefunction and derive a
criterion for the existence of a exciton. We also systematically
investigate the effect of impurities on the coherent motion of an exciton. The
coherence is measured by a suitably defined electron-hole correlation function.
It is shown that, for impurities with an on-site potential, a crossover
behavior will occur if the impurity strength is comparable to the bandwidth of
the exciton, corresponding to exciton localization. For a charged impurity with
a spatially extended potential, in addition to localization the exciton will
dissociate into an uncorrelated electron-hole pair when the impurity is
sufficiently strong to overcome the Coulomb interaction which binds the
electron-hole pair. Interchain coupling effects are also discussed by
considering two polymer chains coupled through nearest-neighbor interchain
hopping and interchain Coulomb interaction . Within the
matrix scattering formalism, for every center-of-mass momentum, we find two
poles determined only by , which correspond to the interchain
excitons. Finally, the exciton state is used to study the charge transfer from
a polymer chain to an adjacent dopant molecule.Comment: 24 pages, 23 eps figures, pdf file of the paper availabl
Electron correlation effects in electron-hole recombination in organic light-emitting diodes
We develop a general theory of electron--hole recombination in organic light
emitting diodes that leads to formation of emissive singlet excitons and
nonemissive triplet excitons. We briefly review other existing theories and
show how our approach is substantively different from these theories. Using an
exact time-dependent approach to the interchain/intermolecular charge-transfer
within a long-range interacting model we find that, (i) the relative yield of
the singlet exciton in polymers is considerably larger than the 25% predicted
from statistical considerations, (ii) the singlet exciton yield increases with
chain length in oligomers, and, (iii) in small molecules containing nitrogen
heteroatoms, the relative yield of the singlet exciton is considerably smaller
and may be even close to 25%. The above results are independent of whether or
not the bond-charge repulsion, X_perp, is included in the interchain part of
the Hamiltonian for the two-chain system. The larger (smaller) yield of the
singlet (triplet) exciton in carbon-based long-chain polymers is a consequence
of both its ionic (covalent) nature and smaller (larger) binding energy. In
nitrogen containing monomers, wavefunctions are closer to the noninteracting
limit, and this decreases (increases) the relative yield of the singlet
(triplet) exciton. Our results are in qualitative agreement with
electroluminescence experiments involving both molecular and polymeric light
emitters. The time-dependent approach developed here for describing
intermolecular charge-transfer processes is completely general and may be
applied to many other such processes.Comment: 19 pages, 11 figure
mer-Bis[3,5-difluoro-2-(2-pyridyl)phenyl-κ2 C 1,N]{5-(2-pyridyl-κN)-3-[3-(4-vinylbenzyloxy)phenyl]-1,2,4-triazol-1-ido}iridium(III) methanol solvate
In the title compound, [Ir(C11H6F2N)2(C22H17N4O)]·CH3OH, the coordination at iridium is essentially octahedral, but with distortions associated with the bite angles of the ligands [76.25 (9)–80.71 (12)°] and the differing trans influences of C and N ligands [Ir—N = 2.04 Å (average) trans to N but 2.14 Å trans to C]. All three bidentate ligands have coordinating ring systems that are almost coplanar [interplanar angles = 1.7 (1)–3.8 (2)°]. The vinylbenzyl group is disordered over two positions with occupations of 0.653 (4) and 0.347 (4). The methanol solvent molecule is involved in a classical O—H⋯N hydrogen bond to a triazole N atom
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