Polar distortions in solids give rise to the well-known functionality of switchable macroscopic polarisation in ferroelectrics and, when combined with strong spin-orbit coupling, can mediate giant spin splittings of electronic states. While typically
found in insulators, ferroelectric-like distortions can remain robust against increasing itineracy, giving rise to so-called polar metals. Here, we investigate the temperature-dependent electronic structure of Ca$_3$Ru$_2$O$_7$, a correlated oxide metal in which octahedral tilts and rotations combine to mediate pronounced polar distortions. Our angle-resolved photoemission measurements reveal the destruction of a large hole-like Fermi surface upon cooling through a coupled structural and spin-reorientation transition at 48 K, accompanied by a sudden onset of quasiparticle coherence. We demonstrate how these result from band hybridisation mediated by a hidden Rashba-type spin-orbit coupling. This is enabled by the bulk structural distortions and unlocked when the spin reorients perpendicular to the local symmetry-breaking potential at the Ru sites. We argue that the electronic energy gain associated with the band hybridisation is actually the key driver for the phase transition, reflecting a delicate interplay between spin-orbit coupling and strong electronic correlations, and revealing a new route to control magnetic ordering in solids.
Iron-based chalcogenides are complex superconducting systems in which orbitally-dependent electronic correlations play an important role. Here, using high-resolution angle-resolved photoemission spectroscopy, we investigate the effect of these electr
onic correlations outside the nematic phase in the tetragonal phase of superconducting FeSe1-xSx (x = 0; 0:18; 1). With increasing sulfur substitution, the Fermi velocities increase significantly and the band renormalizations are suppressed towards a factor of 1.5-2 for FeS. Furthermore, the chemical pressure leads to an increase in the size of the quasi-two dimensional Fermi surface, compared with that of FeSe, however, it remains smaller than the predicted one from first principle calculations for FeS. Our results show that the isoelectronic substitution is an effective way to tune electronic correlations in FeSe1-xSx, being weakened for FeS with a lower superconducting transition temperature. This suggests indirectly that electronic correlations could help to promote higher-Tc superconductivity in FeSe.
Employing a 10-orbital tight binding model, we present a new set of hopping parameters fitted directly to our latest high resolution angle-resolved photoemission spectroscopy (ARPES) data for the high temperature tetragonal phase of FeSe. Using these
parameters we predict a large 10 meV shift of the chemical potential as a function of temperature. In order to confirm this large temperature dependence, we performed ARPES experiments on FeSe and observed a $sim$25 meV rigid shift to the chemical potential between 100 K and 300 K. This unexpectedly strong shift has important implications for theoretical models of superconductivity and of nematic order in FeSe materials.
We present Angle-Resolved Photoemission Spectroscopy measurements of the quasi-one dimensional superconductor K$_2$Cr$_3$As$_3$. We find that the Fermi surface contains two Fermi surface sheets, with linearly dispersing bands not displaying any signi
ficant band renormalizations. The one-dimensional band dispersions display a suppression of spectral intensity approaching the Fermi level according to a linear power law, over an energy range of ~200 meV. This is interpreted as a signature of Tomonoga-Luttinger liquid physics, which provides a new perspective on the possibly unconventional superconductivity in this family of compounds.
Magnetoresistivity r{ho}xx and Hall resistivity r{ho}xy in ultra high magnetic fields up to 88T are measured down to 0.15K to clarify the multiband electronic structure in high-quality single crystals of superconducting FeSe. At low temperatures and
high fields we observe quantum oscillations in both resistivity and Hall effect, confirming the multiband Fermi surface with small volumes. We propose a novel and independent approach to identify the sign of corresponding cyclotron orbit in a compensated metal from magnetotransport measurements. The observed significant differences in the relative amplitudes of the quantum oscillations between the r{ho}xx and r{ho}xy components, together with the positive sign of the high-field r{ho}xy , reveal that the largest pocket should correspond to the hole band. The low-field magnetotransport data in the normal state suggest that, in addition to one hole and one almost compensated electron bands, the orthorhombic phase of FeSe exhibits an additional tiny electron pocket with a high mobility.
We present a comprehensive study of the evolution of the nematic electronic structure of FeSe using high resolution angle-resolved photoemission spectroscopy (ARPES), quantum oscillations in the normal state and elastoresistance measurements. Our hig
h resolution ARPES allows us to track the Fermi surface deformation from four-fold to two-fold symmetry across the structural transition at ~87 K which is stabilized as a result of the dramatic splitting of bands associated with dxz and dyz character. The low temperature Fermi surface is that a compensated metal consisting of one hole and two electron bands and is fully determined by combining the knowledge from ARPES and quantum oscillations. A manifestation of the nematic state is the significant increase in the nematic susceptibility as approaching the structural transition that we detect from our elastoresistance measurements on FeSe. The dramatic changes in electronic structure cannot be explained by the small lattice effects and, in the absence of magnetic fluctuations above the structural transition, points clearly towards an electronically driven transition in FeSe stabilized by orbital-charge ordering.
We report the observation of the de Haas-van Alphen effect in IrTe2 measured using torque magnetometry at low temperatures down to 0.4 K and in high magnetic fields up to 33T. IrTe2 undergoes a major structural transition around 283 K due to the form
ation of planes of Ir and Te dimers that cut diagonally through the lattice planes, with its electronic structure predicted to change significantly from a layered system with predominantly three-dimensional character to a tilted quasi-two dimensional Fermi surface. Quantum oscillations provide direct confirmation of this unusual tilted Fermi surface and also reveal very light quasiparticle masses (less than 1 me), with no significant enhancement due to electronic correlations. We find good agreement between the angular dependence of the observed and calculated de Haas-van Alphen frequencies, taking into account the contribution of different structural domains that form while cooling IrTe2.
