222 research outputs found
Phase Transition in a One-Dimensional Extended Peierls-Hubbard Model with a Pulse of Oscillating Electric Field: II. Linear Behavior in Neutral-to-Ionic Transition
Dynamics of charge density and lattice displacements after the neutral phase
is photoexcited is studied by solving the time-dependent Schr\"odinger equation
for a one-dimensional extended Peierls-Hubbard model with alternating
potentials. In contrast to the ionic-to-neutral transition studied previously,
the neutral-to-ionic transition proceeds in an uncooperative manner as far as
the one-dimensional system is concerned. The final ionicity is a linear
function of the increment of the total energy. After the electric field is
turned off, the electronic state does not significantly change, roughly keeping
the ionicity, even if the transition is not completed, because the ionic
domains never proliferate. As a consequence, an electric field with frequency
just at the linear absorption peak causes the neutral-to-ionic transition the
most efficiently. These findings are consistent with the recent experiments on
the mixed-stack organic charge-transfer complex, TTF-CA. We artificially modify
or remove the electron-lattice coupling to discuss the origin of such
differences between the two transitions.Comment: 17 pages, 9 figure
Charge-Transfer Excitations in One-Dimensional Dimerized Mott Insulators
We investigate the optical properties of one-dimensional (1D) dimerized Mott
insulators using the 1D dimerized extended Hubbard model. Numerical
calculations and a perturbative analysis from the decoupled-dimer limit clarify
that there are three relevant classes of charge-transfer (CT) states generated
by photoexcitation: interdimer CT unbound states, interdimer CT exciton states,
and intradimer CT exciton states. This classification is applied to
understanding the optical properties of an organic molecular material,
1,3,5-trithia-2,4,6-triazapentalenyl (TTTA), which is known for its
photoinduced transition from the dimerized spin-singlet phase to the regular
paramagnetic phase. We conclude that the lowest photoexcited state of TTTA is
the interdimer CT exciton state and the second lowest state is the intradimer
CT exciton state.Comment: 6 pages, 6 figures, to be published in J. Phys. Soc. Jp
Phase Transition in a One-Dimensional Extended Peierls-Hubbard Model with a Pulse of Oscillating Electric Field: I. Threshold Behavior in Ionic-to-Neutral Transition
Photoinduced dynamics of charge density and lattice displacements is
calculated by solving the time-dependent Schr\"odinger equation for a
one-dimensional extended Peierls-Hubbard model with alternating potentials for
the mixed-stack organic charge-transfer complex, TTF-CA. A pulse of oscillating
electric field is incorporated into the Peierls phase of the transfer integral.
The frequency, the amplitude, and the duration of the pulse are varied to study
the nonlinear and cooperative character of the photoinduced transition. When
the dimerized ionic phase is photoexcited, the threshold behavior is clearly
observed by plotting the final ionicity as a function of the increment of the
total energy. Above the threshold photoexcitation, the electronic state reaches
the neutral one with equidistant molecules after the electric field is turned
off. The transition is initiated by nucleation of a metastable neutral domain,
for which an electric field with frequency below the linear absorption peak is
more effective than that at the peak. When the pulse is strong and short, the
charge transfer takes place on the same time scale with the disappearance of
dimerization. As the pulse becomes weak and long, the dimerization-induced
polarization is disordered to restore the inversion symmetry on average before
the charge transfer takes place to bring the system neutral. Thus, a
paraelectric ionic phase is transiently realized by a weak electric field. It
is shown that infrared light also induces the ionic-to-neutral transition,
which is characterized by the threshold behavior.Comment: 24 pages, 11 figure
Electronic and Lattice Dynamics in The Photoinduced Ionic-to-Neutral Phase Transition in a One-Dimensional Extended Peierls-Hubbard Model
Real-time dynamics of charge density and lattice displacements is studied
during photoinduced ionic-to-neutral phase transitions by using a
one-dimensional extended Peierls-Hubbard model with alternating potentials for
the one-dimensional mixed-stack charge-transfer complex, TTF-CA. The
time-dependent Schr\"odinger equation and the classical equation of motion are
solved for the electronic and lattice parts, respectively. We show how neutral
domains grow in the ionic background. As the photoexcitation becomes intense,
more neutral domains are created. Above threshold intensity, the neutral phase
is finally achieved. After the photoexcitation, ionic domains with wrong
polarization also appear. They quickly reduce the averaged staggered lattice
displacement, compared with the averaged ionicity. As the degree of initial
lattice disorder increases, more solitons appear between these ionic domains
with different polarizations, which obstruct the growth of neutral domains and
slow down the transition.Comment: 9 pages, 10 figures, submitted to J. Phys. Soc. Jp
Ultrahigh field electron cyclotron resonance absorption in InMnAs films
We have carried out an ultrahigh field cyclotron resonance study of -type
InMnAs films, with Mn composition ranging from 0 to 12%, grown
on GaAs by low temperature molecular beam epitaxy. We observe that the electron
cyclotron resonance peak shifts to lower field with increasing . A detailed
comparison of experimental results with calculations based on a modified
Pidgeon-Brown model allows us to estimate the {\em s-d} and {\em p-d} exchange
coupling constants, and , for this important III-V dilute
magnetic semiconductor system.Comment: 4 pages, 4 figure
Anisotropic Magnetoresistance in GaMnAs
We have measured the magnetoresistance in a series of GaMnAs
samples with 0.033 0.053 for three mutually orthogonal orientations
of the applied magnetic field. The spontaneous resistivity anisotropy (SRA) in
these materials is negative (i.e. the sample resistance is higher when its
magnetization is perpendicular to the measuring current than when the two are
parallel) and has a magnitude on the order of 5% at temperatures near 10K and
below. This stands in contrast to the results for most conventional magnetic
materials where the SRA is considerably smaller in magnitude for those few
cases in which a negative sign is observed. The magnitude of the SRA drops from
its maximum at low temperatures to zero at T in a manner that is consistent
with mean field theory. These results should provide a significant test for
emerging theories of transport in this new class of materials.Comment: 4 pages with 4 figures. Submitted to Physical Review
100â ps time-resolved solution scattering utilizing a wide-bandwidth X-ray beam from multilayer optics
A new method of time-resolved solution scattering utilizing X-ray multilayer optics is presented
Effects of Lattice and Molecular Phonons on Photoinduced Neutral-to-Ionic Transition Dynamics in Tetrathiafulvalene--Chloranil
For electronic states and photoinduced charge dynamics near the neutral-ionic
transition in the mixed-stack charge-transfer complex
tetrathiafulvalene--chloranil (TTF-CA), we review the effects of Peierls
coupling to lattice phonons modulating transfer integrals and Holstein
couplings to molecular vibrations modulating site energies. The former
stabilizes the ionic phase and reduces discontinuities in the phase transition,
while the latter stabilizes the neutral phase and enhances the discontinuities.
To reproduce the experimentally observed ionicity, optical conductivity and
photoinduced charge dynamics, both couplings are quantitatively important. In
particular, strong Holstein couplings to form the highly-stabilized neutral
phase are necessary for the ionic phase to be a Mott insulator with large
ionicity. A comparison with the observed photoinduced charge dynamics indicates
the presence of strings of lattice dimerization in the neutral phase above the
transition temperature.Comment: 9 pages, 7 figures, accepted for publication in J. Phys. Soc. Jp
Photoinduced metallic properties of one-dimensional strongly correlated electron systems
We study photoinduced optical responses of one-dimensional strongly
correlated electron systems. The optical conductivity spectra are calculated
for the ground state and a photoexcited state in the one-dimensional Hubbard
model at half filling by using the exact diagonalization method. It is found
that, in the Mott insulator phase, the photoexcited state has large spectral
weights including the Drude weight below the optical gap. As a consequence, the
spectral weight above the optical gap is largely reduced. These results imply
that a metallic state is induced by photoexcitation. Comparison between the
photoexcited and hole-doped states shows that the photoexcitation is similar to
chemical doping.Comment: 4 pages, 4 figures, submitted to J. Phys. Soc. Jp
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