We address the kinetic competition between charge striped order and superconductivity in La$_{1.675}$Eu$_{0.2}$Sr$_{0.125}$CuO$_{4}$. Ultrafast optical excitation is tuned to a mid-infrared vibrational resonance that destroys charge order and promptl
y establishes transient coherent interlayer coupling in this material. This effect is evidenced by the appearance of a longitudinal plasma mode reminiscent of a Josephson plasma resonance. We find that coherent interlayer coupling can be generated up to the charge order transition $T_{CO} approx$ 80 K, far above the equilibrium superconducting transition temperature of any lanthanide cuprate. Two key observations are extracted from the relaxation kinetics of the interlayer coupling. Firstly, the plasma mode relaxes through a collapse of its coherence length and not its density. Secondly, two distinct kinetic regimes are observed for this relaxation, above and below spin order transition $T_{SO} =$ 25 K. Especially, the temperature independent relaxation rate observed below $T_{SO}$ is anomalous and suggests coexistence of superconductivity and stripes rather than competition. Both observations support arguments that a low temperature coherent stripe (or pair density wave) phase suppresses c-axis tunnelling by disruptive interference rather than by depleting the condensate.
We use midinfrared pulses with stable carrier-envelope phase offset to drive molecular vibrations in the charge transfer salt ET-F2TCNQ, a prototypical one-dimensional Mott insulator. We find that the Mott gap, which is probed resonantly with 10 fs l
aser pulses, oscillates with the pump field. This observation reveals that molecular excitations can coherently perturb the electronic on-site interactions (Hubbard U) by changing the local orbital wave function. The gap oscillates at twice the frequency of the vibrational mode, indicating that the molecular distortions couple quadratically to the local charge density.
Most available theories for correlated electron transport are based on the Hubbard Hamiltonian. In this effective theory, renormalized hopping and interaction parameters only implicitly incorporate the coupling of correlated charge carriers to micros
copic degrees of freedom. Unfortunately, no spectroscopy can individually probe such renormalizations, limiting the applicability of Hubbard models. We show here that the role of each individual degree of freedom can be made explicit by using a new experimental technique, which we term quantum modulation spectroscopy and we demonstrate here in the one-dimensional Mott insulator ET-F2TCNQ. We explore the role on the charge hopping of two localized molecular modes, which we drive with a mid infrared optical pulse. Sidebands appear in the modulated optical spectrum, and their linshape is fitted with a model based on the dynamic Hubbard Hamiltonian. A striking asymmetry between the renormalization of doublons and holons is revealed. The concept of quantum modulation spectroscopy can be used to systematically deconstruct Hubbard Hamiltonians in many materials, exposing the role of any mode, electronic or magnetic, that can be driven to large amplitude with a light field.
We report on a photo-induced transient state of YBa2Cu2O6+x in which transport perpendicular to the Cu-O planes becomes highly coherent. This effect is achieved by excitation with mid-infrared optical pulses, tuned to the resonant frequency of apical
oxygen vibrations, which modulate both lattice and electronic properties. Below the superconducting transition temperature Tc, the equilibrium signatures of superconducting interlayer coupling are enhanced. Most strikingly, the optical excitation induces a new reflectivity edge at higher frequency than the equilibrium Josephson plasma resonance, with a concomitant enhancement of the low frequency imaginary conductivity. Above Tc, the incoherent equilibrium conductivity becomes highly coherent, with the appearance of a reflectivity edge and a positive imaginary conductivity that increases with decreasing frequency. These features are observed up to room temperature in YBa2Cu2O6.45 and YBa2Cu2O6.5. The data above Tc can be fitted by hypothesizing that the light re-establishes a transient superconducting state over only a fraction of the solid, with a lifetime of a few picoseconds. Non-superconducting transport could also explain these observations, although one would have to assume transient carrier mobilities near 10^4 cm^2/(V.sec) at 100 K, with a density of charge carriers similar to the below Tc superfluid density. Our results are indicative of highly unconventional non-equilibrium physics and open new prospects for optical control of complex solids.
We observe charge-order fluctuations in the quasi-two-dimensional organic superconductor $beta^{primeprime}$-(BEDT-TTF)2 SF5 CH2 CF2 SO3 both by means of vibrational spectroscopy, locally probing the fluctuating charge order, and investigating the in
-plane dynamical response by infrared reflectance spectroscopy. The decrease of effective electronic interaction in an isostructural metal suppresses both charge-order fluctuations and superconductivity, pointing on their interplay. We compare the results of our experiments with calculations on the extended Hubbard model.
The temperature dependences of the electric-transport properties of the two-dimensional organic conductors beta-(BEDT-TTF)2SF5CH2CF2SO3, beta-(d8-BEDT-TTF)2SF5CH2CF2SO3, and beta-(BEDT-TTF)2SF5CHFSO3 are measured by dc methods in and perpendicular to
the highly-conducting plane. Microwave measurements are performed at 24 and 33.5 GHz to probe the high-frequency behavior from room temperature down to 2 K. Superconductivity is observed in beta-(BEDT-TTF)2SF5CH2CF2SO3 and its deuterated analogue. Although all the compounds remain metallic down to low-temperatures, they are close to a charge-order transition. This leads to deviations from a simple Drude behavior of the optical conductivity which become obvious already in the microwave range. In beta-(BEDT-TTF)2SF5CH2CF2SO3, for instance, charge fluctuations cause an increase in microwave resistivity for T < 20 K which is not detected in dc measurements. beta-(BEDT-TTF)2SF5CHFSO3 exhibits a simple metallic behavior at all frequencies. In the dc transport, however, we observe indications of localization in the perpendicular direction.
Measurements of electrodynamic response of of spin glass AuFe films in comparison with pure gold films are performed at frequencies from 0.3 THz (10 cm-1) up to 1000 THz (33000 cm-1) using different spectroscopic methods. At room temperatures the spe
ctra of pure gold and of AuFe are typically metallic with the scattering rate of carriers in AuFe being significantly enlarged due to scattering on localized magnetic moments of Fe ions. In the spin-glass phase of AuFe at T = 5 K a pseudogap in the conductivity spectrum is detected with the magnitude close to the Ruderman-Kittel-Kasuya-Yosida (RKKY) energy for AuFe: Delta(RKKY) = 2.2 meV. The origin of the pseudogap is associated with partial localization of electrons which mediate the RKKY interaction between localized magnetic Fe centers.
