Electron relaxation in metals: Theory and exact analytical solutions

The non-equilibrium dynamics of electrons is of a great experimental and theoretical value providing important microscopic parameters of the Coulomb and electron-phonon interactions in metals and other cold plasmas. Because of the mathematical complexity of collision integrals theories of electron relaxation often rely on the assumption that electrons are in a "quasi-equilibrium" (QE) with a time-dependent temperature, or on the numerical integration of the time-dependent Boltzmann equation. We transform the integral Boltzmann equation to a partial differential Schroedinger-like equation with imaginary time in a one-dimensional "coordinate" space reciprocal to energy which allows for exact analytical solutions in both cases of electron-electron and electron-phonon relaxation. The exact relaxation rates are compared with the QE relaxation rates at high and low temperatures.Comment: Citation list has been extended. The paper is submitted to the Physical Review

Photoinduced melting of superconductivity in the high-Tc superconductor La2-xSrxCuO4 probed by time-resolved optical and THz techniques

Dynamics of depletion and recovery of superconducting state in La2-xSrxCuO_4 thin films is investigated utilizing optical pump-probe and optical pump - THz probe techniques as a function of temperature and excitation fluence. The absorbed energy density required to suppress superconductivity is found to be about 8 times higher than the thermodynamically determined condensation energy density and nearly temperature independent between 4 and 25 K. These findings indicate that during the time when superconducting state suppression takes place (~0.7 ps), a large part (nearly 90%) of the energy is transferred to the phonons with energy lower than twice the maximum value of of the SC gap and only 10% is spent on Cooper pair breaking.Comment: 8 pages, 5 figure

Relaxation Dynamics of Photoinduced Changes in the Superfluid Weight of High-Tc Superconductors

In the transient state of d-wave superconductors, we investigate the temporal variation of photoinduced changes in the superfluid weight. We derive the formula that relates the nonlinear response function to the nonequilibrium distribution function. The latter qunatity is obtained by solving the kinetic equation with the electron-electron and the electron-phonon interaction included. By numerical calculations, a nonexponential decay is found at low temperatures in contrast to the usual exponential decay at high temperatures. The nonexponential decay originates from the nonmonotonous temporal variation of the nonequilibrium distribution function at low energies. The main physical process that causes this behavior is not the recombination of quasiparticles as previous phenomenological studies suggested, but the absorption of phonons.Comment: 18 pages, 12 figures; to be published in J. Phys. Soc. Jpn. Vol. 80, No.

Combination quantum oscillations in canonical single-band Fermi liquids

Chemical potential oscillations mix individual-band frequencies of the de Haas-van Alphen (dHvA) and Shubnikov-de Haas (SdH) magneto-oscillations in canonical low-dimensional multi-band Fermi liquids. We predict a similar mixing in canonical single-band Fermi liquids, which Fermi-surfaces have two or more extremal cross-sections. Combination harmonics are analysed using a single-band almost two-dimensional energy spectrum. We outline some experimental conditions allowing for resolution of combination harmonics

Dynamics of broken symmetry nodal and anti-nodal excitations in Bi_{2} Sr_{2} CaCu_{2} O_{8+\delta} probed by polarized femtosecond spectroscopy

The dynamics of excitations with different symmetry is investigated in the superconducting (SC) and normal state of the high-temperature superconductor Bi$_{2}$Sr$_{2}$CaCu$_{2}$O$_{8+\delta}$ (Bi2212) using optical pump-probe (Pp) experiments with different light polarizations at different doping levels. The observation of distinct selection rules for SC excitations, present in A$_{{\rm 1g}}$ and B$_{{\rm 1g}}$ symmetries, and for the PG excitations, present in A$_{{\rm 1g}}$ and B$_{{\rm 2g}}$ symmetries, by the probe and absence of any dependence on the pump beam polarization leads to the unequivocal conclusion of the existence of a spontaneous spatial symmetry breaking in the pseudogap (PG) state

Magnetic quantum oscillations in nanowires

Analytical expressions for the magnetization and the longitudinal conductivity of nanowires are derived in a magnetic field, B. We show that the interplay between size and magnetic field energy-level quantizations manifests itself through novel magnetic quantum oscillations in metallic nanowires. There are three characteristic frequencies of de Haas-van Alphen (dHvA) and Shubnikov-de Haas (SdH) oscillations, F=F_0,F_1, and F_2 in contrast with a single frequency F'_0 in simple bulk metals. The amplitude of oscillations is strongly enhanced in some "magic" magnetic fields. The wire cross-section S can be measured along with the Fermi surface cross-section, S_F

Quasiparticle relaxation dynamics in heavy fermion compounds

We present the first femtosecond studies of electron-phonon (e-ph) thermalization in heavy fermion compounds. The e-ph thermalization time tau_{ep} increases below the Kondo temperature by more than two orders of magnitude as T = 0 K is approached. Analysis using the two-temperature model and numerical simulations based on Boltzmann's equations suggest that this anomalous slowing down of the e-ph thermalization derives from the large electronic specific heat and the suppresion of scattering between heavy electrons and phonons.Comment: 4 pages, 3 figures, accepted for publication in Phys. Rev. Let

Electrophoresis of a rod macroion under polyelectrolyte salt: Is mobility reversed for DNA?

By molecular dynamics simulation, we study the charge inversion phenomenon of a rod macroion in the presence of polyelectrolyte counterions. We simulate electrophoresis of the macroion under an applied electric field. When both counterions and coions are polyelectrolytes, charge inversion occurs if the line charge density of the counterions is larger than that of the coions. For the macroion of surface charge density equal to that of the DNA, the reversed mobility is realized either with adsorption of the multivalent counterion polyelectrolyte or the combination of electrostatics and other mechanisms including the short-range attraction potential or the mechanical twining of polyelectrolyte around the rod axis.Comment: 8 pages, 5 figures, Applied Statistical Physics of Molecular Engineering (Mexico, 2003). Journal of Physics: Condensed Matters, in press (2004). Journal of Physics: Condensed Matters, in press (2004