791 research outputs found

    Correlated-electron description of the photophysics of thin films of π\pi-conjugated polymers

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    We extend Mulliken's theory of ground state charge transfer in a donor-acceptor complex to excited state charge transfer between pairs of identical π\pi-conjugated oligomers, one of which is in the optically excited state and the other in the ground state, leading to the formation of a charge-transfer exciton. Within our theory, optical absorptions from the charge-transfer exciton should include a low energy intermolecular charge-transfer excitation, as well as distinct intramolecular excitations from both the neutral delocalized exciton component and the Coulombically bound polaron-pair component of the charge-transfer exciton. We report high order configuration-interaction calculations for pairs of oligomers of poly-paraphenylenevinylene (PPV) that go beyond our previous single configuration-interaction calculation and find all five excited state absorptions predicted using heuristic arguments based on the Mulliken concept. Our calculated excited state absorption spectrum exhibits strong qualitative agreement with the complete wavelength-dependent ultrafast photoinduced absorption in films of PPV derivatives, suggesting that a significant fraction of the photoinduced absorption here is from the charge-transfer exciton. We make detailed comparisons to experiments, and a testable experimental prediction

    Effect of interchain coupling on conducting polymer luminescence: excimers in derivatives of poly(phenylene vinylene)

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    Optical excitation of a chain in a polymer film may result in formation of an excimer, a superposition of on-chain excitons and charge-transfer excitons on the originally excited chain and a neighboring chain. The excimer emission is red-shifted compared to that of an on-chain exciton by an amount depending on the interchain coupling t⊥t_\perp. Setting up the excimer wavefunction and calculating the red shift, we determine average t⊥t_\perp values, referred to a monomer, of 0.52 eV and 0.16 eV for poly(2,5-hexyloxy pp-phenylene cyanovinylene), CN-PPV, and poly[2-methoxy, 5-(2'-ethyl-hexyloxy)-1, 4 p-phenylene vinylene], MEH-PPV, respectively, and use them to determine the effect of interchain distance on the emission.Comment: 10 pages, RevTeX, 1 PS figure, replaced version of cond-mat/9707095, accepted for publication in Phys. Rev. B, Rapid Communicatio

    Hot-electron effect in spin dephasing in nn-type GaAs quantum wells

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    We perform a study of the effect of the high in-plane electric field on the spin precession and spin dephasing due to the D'yakonov-Perel' mechanism in nn-type GaAs (100) quantum wells by constructing and numerically solving the kinetic Bloch equations. We self-consistently include all of the scattering such as electron-phonon, electron-non-magnetic impurity as well as the electron-electron Coulomb scattering in our theory and systematically investigate how the spin precession and spin dephasing are affected by the high electric field under various conditions. The hot-electron distribution functions and the spin correlations are calculated rigorously in our theory. It is found that the D'yakonov-Perel' term in the electric field provides a non-vanishing effective magnetic field that alters the spin precession period. Moreover, spin dephasing is markedly affected by the electric field. The important contribution of the electron-electron scattering to the spin dephasing is also discussed.Comment: 11 pages, 11 figures, accepted for publication in Phys. Rev.

    Investigation of acceptor levels and hole scattering mechanisms in p-gallium selenide by means of transport measurements under pressure

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    The effect of pressure on acceptor levels and hole scattering mechanisms in p-GaSe is investigated through Hall effect and resistivity measurements under quasi-hydrostatic conditions up to 4 GPa. The pressure dependence of the hole concentration is interpreted through a carrier statistics equation with a single (nitrogen) or double (tin) acceptor whose ionization energies decrease under pressure due to the dielectric constant increase. The pressure effect on the hole mobility is also accounted for by considering the pressure dependencies of both the phonon frequencies and the hole-phonon coupling constants involved in the scattering rates.Comment: 13 pages, Latex, 4 ps figures. to appear in High Pressure Research 69 (1997

    Evidence for Excimer Photoexcitations in an Ordered {\pi}-Conjugated Polymer Film

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    We report pressure-dependent transient picosecond and continuous-wave photomodulation studies of disordered and ordered films of 2-methoxy-5-(2-ethylhexyloxy) poly(para-phenylenevinylene). Photoinduced absorption (PA) bands in the disordered film exhibit very weak pressure dependence and are assigned to intrachain excitons and polarons. In contrast, the ordered film exhibits two additional transient PA bands in the midinfrared that blueshift dramatically with pressure. Based on high-order configuration interaction calculations we ascribe the PA bands in the ordered film to excimers. Our work brings insight to the exciton binding energy in ordered films versus disordered films and solutions. The reduced exciton binding energy in ordered films is due to new energy states appearing below the continuum band threshold of the single strand.Comment: 5.5 pages, 5 figure

    A Retrospective Analysis Of Risk Factors That Influence Intravenous Busulfan Kinetics In Adult Patients

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