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We study the incoherent recombination of topological defects created during a rapid quench of a charge-density-wave system through the electronic ordering transition. Using a specially devised three-pulse femtosecond optical spectroscopy technique we follow the evolution of the order parameter over a wide range of time scales. By careful consideration of thermal processes we can clearly identify intrinsic topological defect annihilation processes on a time scale ~30 ps and find a possible signature of extrinsic defect-dominated relaxation dynamics occurring on longer time scales. [ABSTRACT FROM AUTHOR]

We investigate the relaxation dynamics of nonequilibrium carriers in organic conductors κ-(BEDT-TTF)2Cu[N(CN)2]X (X = Br and Cl) using ultrafast time-resolved optical spectroscopy. The dynamics for both salts show similar temperature dependences, which is well characterized by the carrier relaxation across the pseudogap (PG) of the magnitude ΔPG ≈ 16 meV for Br salt and 7.0 meV for Cl salt. On the other hand, only the Br salt shows an abrupt increase of the decay time at low temperature, indicating an additional decay component associated with the superconducting (SC) gap below Tc. The fluence dependent dynamics at low temperature evidences the superposition of the SC component onto the PG component. These results indicate a metallic-insulating phase separation in the Br salt triggered by photoexcited nonequilibrium carriers. [ABSTRACT FROM AUTHOR]

We use femtosecond spectroscopy to investigate the quasiparticle relaxation and low-energy electronic structure in a nearly optimally doped pnictide superconductor with T{c}=49.5 K. Multiple relaxation processes are evident, with distinct superconducting state quasiparticle recombination dynamics exhibiting a T-dependent superconducting gap, and a clear "pseudogaplike" feature with an onset above 180 K indicating the existence of a temperature-independent gap of magnitude Delta{PG}=61+/-9 meV above T{c}. Both the superconducting and pseudogap components show saturation as a function of fluence with distinct saturation fluences 4 and 40 microJ/cm{2}, respectively.

We report on a study of the interactions between holes and molecular vibrations on dry DNA using photoinduced infrared absorption spectroscopy. Laser photoexcited holes are found to have a room-temperature lifetime in excess of tau > 1 ms, clearly indicating the presence of localization. However, from a quantitative model analysis of the frequency shifts of vibrational modes caused by the holes, we find the hole-vibrational coupling constant to be relatively small, lambda approximately 0.2. This interaction leads to a change in the conformational energy of DeltaE0 approximately 0.015 eV, which is too small to cause self-trapping at room temperature. We conclude that, at least in the dry (A) form, DNA is best understood in terms of a double chain of coupled quantum dots arising from the pseudorandom chain sequence of base pairs, in which Anderson localization prevents the formation of a metallic state.

Critical exponents at the ferromagnetic transition were measured for the first time in an organic ferromagnetic material tetrakis(dimethylamino)ethylene fullerene[60] (TDAE- C(60)). From a complete magnetization-temperature-field data set near T(c) = 16.1+/-0.05, we determine the susceptibility and magnetization critical exponents gamma = 1.22+/-0.02 and beta = 0.75+/-0.03, respectively, and the field vs magnetization exponent at T(c) of delta = 2.28+/-0.14. Hyperscaling is found to be violated by Omega identical with d(')-d approximately -1/4, suggesting that the onset of ferromagnetism can be related to percolation of a particular contact configuration of C(60) molecular orientations.