We report angle-resolved photoelectron spectroscopy measurements of the quantum critical metal Sr3Ru2O7 revealing itinerant Ru 4d-states confined over large parts of the Brillouin zone to an energy range of < 6 meV, nearly three orders of magnitude lower than the bare band width. We show that this energy scale agrees quantitatively with a characteristic thermodynamic energy scale associated with quantum criticality and illustrate how it arises from the hybridization of light and strongly renormalized, heavy quasiparticle bands. For the largest Fermi surface sheet we find a marked k-dependence of the renormalization and show that it correlates with the Ru 4d - O 2p hybridization.
The intriguing idea that strongly interacting electrons can generate spatially inhomogeneous electronic liquid crystalline phases is over a decade old, but these systems still represent an unexplored frontier of condensed matter physics. One reason is that visualization of the many-body quantum states generated by the strong interactions, and of the resulting electronic phases, has not been achieved. Soft condensed matter physics was transformed by microscopies that allowed imaging of real-space structures and patterns. A candidate technique for obtaining equivalent data in the purely electronic systems is Spectroscopic Imaging Scanning Tunneling Microscopy (SI-STM). The core challenge is to detect the tenuous but heavy k-space components of the many-body electronic state simultaneously with its r-space constituents. Sr3Ru2O7 provides a particularly exciting opportunity to address these issues. It possesses (i) a very strongly renormalized heavy d-electron Fermi liquid and (ii) exhibits a field-induced transition to an electronic liquid crystalline phase. Finally, as a layered compound, it can be cleaved to present an excellent surface for SI-STM.
Sr3Ru2O7 belongs to the family of layered strontium ruthenates and exhibits a range of unusual emergent properties, such as electron nematic behavior and metamagnetism. Here, we show that epitaxial film strain significantly modifies these phenomena. In particular, we observe enhanced magnetic interactions and an electron nematic phase that extends to much higher temperatures and over a larger magnetic field range than in bulk single crystals. Furthermore, the films show an unusual anisotropic non-Fermi liquid behavior that is controlled by the direction of the applied magnetic field. At high magnetic fields the metamagnetic transition to a ferromagnetic phase recovers isotropic Fermi-liquid behavior. The results support the interpretation that these phenomena are linked to the special features of the Fermi surface, which can be tuned by both film strain and an applied magnetic field.
We report on the results of a high-resolution angle-resolved photoemission (ARPES) study on the ordered surface alloy CePt5. The temperature dependence of the spectra show the formation of the coherent low-energy heavy-fermion band near the Fermi level. This experimental data is supported by a multi-band model calculation in the framework of the dynamical mean field theory (DMFT).
The superconducting order parameter of the first heavy-fermion superconductor CeCu2Si2 is currently under debate. A key ingredient to understand its superconductivity and physical properties is the quasiparticle dispersion and Fermi surface, which remains elusive experimentally. Here we present measurements from angle-resolved photoemission spectroscopy. Our results emphasize the key role played by the Ce 4f electrons for the low-temperature Fermi surface, highlighting a band-dependent conduction-f electron hybridization. In particular, we find a very heavy quasi-two-dimensional electron band near the bulk X point and moderately heavy three-dimensional hole pockets near the Z point. Comparison with theoretical calculations reveals the strong local correlation in this compound, calling for further theoretical studies. Our results provide the electronic basis to understand the heavy fermion behavior and superconductivity; implications for the enigmatic superconductivity of this compound are also discussed.
Optical reflectivity measurements were performed on a single crystal of the d-electron heavy-fermion (HF) metal LiV2O4. The results evidence the highly incoherent character of the charge dynamics for all temperatures above T^* approx 20 K. The spectral weight of the optical conductivity is redistributed over extremely broad energy scales (~ 5 eV) as the quantum coherence of the charge carriers is recovered. This wide redistribution is, in sharp contrast to f-electron Kondo lattice HF systems, characteristic of a metallic system close to a correlation driven insulating state. Our results thus reveal that strong electronic correlation effects dominate the low-energy charge dynamics and heavy quasiparticle formation in LiV2O4. We propose the geometrical frustration, which limits the extension of charge and spin ordering, as an additional key ingredient of the low-temperature heavy-fermion formation in this system.