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Register a new userTerahertz time-domain spectroscopy of transient metallic and superconducting states
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Time-resolved terahertz time-domain spectroscopy (THz-TDS) is an ideal tool for probing photoinduced nonequilibrium metallic and superconducting states. Here, we focus on the interpretation of the two-dimensional response function $Sigma(omega;t)$ that it measures, examining whether it provides an accurate snapshot of the instantaneous optical conductivity, $sigma(omega;t)$. For the Drude model with a time-dependent carrier density, we show that $Sigma(omega;t)$ is not simply related to $sigma(omega;t)$. The difference in the two response functions is most pronounced when the momentum relaxation rate of photocarriers is long, as would be the case in a system that becomes superconducting following pulsed photoexcitation. From the analysis of our model, we identify signatures of photoinduced superconductivity that could be seen by time-resolved THz-TDS.
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We comment on the model proposed by Orenstein and Dodge in arXiv:1506.06758v1, which describes time-domain terahertz measurements of transiently generated, high-electron-mobility (or superconducting) phases of solids. The authors main conclusion is that time-domain terahertz spectroscopy does not measure a response function that is mathematically identical to the transient optical conductivity. We show that although this is correct, the difference between the measured response function and the microscopic optical conductivity is small for realistic experimental parameters. We also show that for the experiments reported by our group on light-induced superconducting-like phases in cuprates and in organic conductors, the time-domain terahertz yields a very good estimate for the optical conductivity.
We measure the anisotropic mid-infrared response of electrons and phonons in bulk YBa2Cu3O7 after femtosecond photoexcitation. A line shape analysis of specific lattice modes reveals their transient occupation and coupling to the superconducting condensate. The apex oxygen vibration is strongly excited within 150 fs demonstrating that the lattice absorbs a major portion of the pump energy before the quasiparticles are thermalized. Our results attest to substantial electron-phonon scattering and introduce a powerful concept probing electron-lattice interactions in a variety of complex materials.
Searching for Kitaev quantum spin liquid (QSL) is a fascinating and challenging problem. Much effort has been devoted to honeycomb lattice candidates with strong spin-orbit coupling in 5d-electron iridates and 4delectron RuCl3. Recently, theoretical studies suggested that the 3d7 Co-based honeycomb materials with high spin state S=3/2 and effective orbital angular momentum L=1 could also be promising candidates of Kitaev QSL. One of the candidates, BaCo2(AsO4)2, was revisited recently. The long range magnetic order in BaCo2(AsO4)2 can be suppressed by very weak in-plane magnetic field, suggesting its proximity to Kitaev QSL. Here we perform time domain terahertz spectroscopy measurement to study the magnetic excitations on BaCo2(AsO4)2. We observe different magnon excitations upon increasing external magnetic field. In particular, the system is easily driven to a field-polarized paramagnetic phase, after the long range magnetic order is suppressed by a weak field Hc 2. The spectra beyond Hc2 are dominated by single magnon and two magnon excitations without showing signature of QSL. We discuss the similarity and difference of the excitation spectra between BaCo2(AsO4)2 and the widely studied Kitaev QSL candidate RuCl3.
We present a maximum-likelihood method for parameter estimation in terahertz time-domain spectroscopy. We derive the likelihood function for a parameterized frequency response function, given a pair of time-domain waveforms with known time-dependent noise amplitudes. The method provides parameter estimates that are superior to other commonly-used methods, and provides a reliable measure of the goodness of fit. We also develop a simple noise model that is parameterized by three dominant sources, and derive the likelihood function for their amplitudes in terms of a set of repeated waveform measurements. We demonstrate the method with applications to material characterization.
We demonstrate terahertz time-domain spectroscopy (THz-TDS) to be an accurate, rapid and scalable method to probe the interaction-induced Fermi velocity renormalization { u}F^* of charge carriers in graphene. This allows the quantitative extraction of all electrical parameters (DC conductivity {sigma}DC, carrier density n, and carrier mobility {mu}) of large-scale graphene films placed on arbitrary substrates via THz-TDS. Particularly relevant are substrates with low relative permittivity (< 5) such as polymeric films, where notable renormalization effects are observed even at relatively large carrier densities (> 10^12 cm-2, Fermi level > 0.1 eV). From an application point of view, the ability to rapidly and non-destructively quantify and map the electrical ({sigma}DC, n, {mu}) and electronic ({ u}F^* ) properties of large-scale graphene on generic substrates is key to utilize this material in applications such as metrology, flexible electronics as well as to monitor graphene transfers using polymers as handling layers.
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