No Arabic abstract
We propose a measurement scheme to directly detect odd-frequency superconductivity via time- and angle-resolved photoelectron fluctuation spectroscopy. The scheme includes two consecutive, non-overlapping probe pulses applied to a superconducting sample. The photoemitted electrons are collected in a momentum-resolved fashion. Correlations between signals with opposite momenta are analyzed. Remarkably, these correlations are directly proportional to the absolute square of the time-ordered anomalous Greens function of the superconductor. This setup allows for the direct detection of the hidden order parameter of odd-frequency pairing. We illustrate this general scheme by concretely analyzing the signal for the prototypical case of two-band superconductors, which are known to exhibit odd-frequency pairing under certain conditions.
A microscopic calculation and symmetry argument reveal superconductivity in the vicinity of parity-violating magnetic order. An augmented cluster magnetic multipole order in a crystal lacking local space inversion parity may break global inversion symmetry, and then, it is classified into an odd-parity multipole order. We investigate unconventional superconductivity induced by an odd-parity magnetic multipole fluctuation in a two-dimensional two-sublattice Hubbard model motivated by Sr$_2$IrO$_4$. We find that even-parity superconductivity is more significantly suppressed by a spin-orbit coupling than that in a globally noncentrosymmetric system. Consequently, two odd-parity superconducting states are stabilized by magnetic multipole fluctuations in a large spin-orbit coupling region. Both of them are identified as $Z_2$ topological superconducting states. The obtained gap function of inter-sublattice pairing shows a gapped/nodal structure protected by nonsymmorphic symmetry. Our finding implies a new family of odd-parity topological superconductors. Candidate materials are discussed.
We formulate a general framework for addressing both odd- and even-frequency superconductivity in Dirac semimetals and demonstrate that the odd-frequency or the Berezinskii pairing can naturally appear in these materials because of the chirality degree of freedom. We show that repulsive frequency-dependent interactions favor the Berezinskii pairing while an attractive electron-electron interaction allows for the BCS pairing. In the case of compensated Dirac and Weyl semimetals, both the conventional BCS and odd-frequency Berezinskii pairings require critical coupling. Since these pairings could originate from physically different mechanisms, our findings pave the way for controlling the realization of the Berezinskii superconductivity in topological semimetals. We also present the density of states with several cusp-like features that can serve as an experimentally verifiable signature of the odd-frequency gap.
We present an Angle-Resolved PhotoElectron Spectroscopy study of the changes in the electronic structure of electron doped Ba(Fe(1-x)Co(x))2As2 across the superconducting phase transition. By changing the polarization of the incoming light, we were able to observe the opening of the gap for the inner hole pocket alpha, and to compare its behavior with the outer hole-like band beta. Measurements along high symmetry directions show that the behavior of beta is consistent with an isotropic gap opening, while slight anisotropies are detected for the inner band alpha. The implications of these results for the s+/- symmetry of the superconducting order parameter are discussed, in relation to the nature of the different iron orbitals contributing to the electronic structure of this multiband system.
In this article we review our angle- and time-resolved photoemission studies (ARPES and trARPES) on various ferropnictides.
We present a time-dependent density-functional method able to describe the photoelectron spectrum of atoms and molecules when excited by laser pulses. This computationally feasible scheme is based on a geometrical partitioning that efficiently gives access to photoelectron spectroscopy in time-dependent density-functional calculations. By using a geometrical approach, we provide a simple description of momentum-resolved photoe- mission including multi-photon effects. The approach is validated by comparison with results in the literature and exact calculations. Furthermore, we present numerical photoelectron angular distributions for randomly oriented nitrogen molecules in a short near infrared intense laser pulse and helium-(I) angular spectra for aligned carbon monoxide and benzene.