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Register a new userProbing dynamics in quantum materials with femtosecond x-rays
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Optical pulses are routinely used to drive dynamical changes in the properties of solids. In quantum materials, many new phenomena have been discovered, including ultrafast transitions between electronic phases, switching of ferroic orders and nonequilibrium emergent behaviors such as photo-induced superconductivity. Understanding the underlying non-equilibrium physics requires detailed measurements of multiple microscopic degrees of freedom at ultrafast time resolution. Femtosecond x-rays are key to this endeavor, as they can access the dynamics of structural, electronic and magnetic degrees of freedom. Here, we cover a series of representative experimental studies in which ultrashort x-ray pulses from free electron lasers have been used, opening up new horizons for materials research.
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We have developed a polarized hard X-ray photoemission (HAXPES) system to study the ground-state symmetry of strongly correlated materials. The linear polarization of the incoming X-ray beam is switched by the transmission-type phase retarder composed of two diamond (100) crystals. The best degree of the linear polarization $P_L$ is $-0.96$, containing the vertical polarization component of 98%. A newly developed low temperature two-axis manipulator enables easy polar and azimuthal rotations to select the detection direction of photoelectrons. The lowest temperature achieved is 9 K, offering us a chance to access the ground state even for the strongly correlated electron systems in cubic symmetry. The co-axial sample monitoring system with the long-working-distance microscope enables us to keep measuring the same region on the sample surface before and after rotation procedures. Combining this sample monitoring system with a micro-focused X-ray beam by means of an ellipsoidal Kirkpatrick-Baez mirror (25 $mu$m $times$ 25 $mu$m (FWHM)), we have demonstrated the polarized valence-band HAXPES on NiO for voltage application as resistive random access memories to reveal the origin of the metallic spectral weight near the Fermi level.
Thermal transport is less appreciated in probing quantum materials in comparison to electrical transport. This article aims to show the pivotal role that thermal transport may play in understanding quantum materials: the longitudinal thermal transport reflects the itinerant quasiparticles even in an electrical insulating phase, while the transverse thermal transport such as thermal Hall and Nernst effect are tightly linked to nontrivial topology. We discuss three types of examples: quantum spin liquids where thermal transport identifies its existence, superconductors where thermal transport reveals the superconducting gap structure, and topological Weyl semimetals where anomalous Nernst effect is a consequence of nontrivial Berry curvature. We conclude with an outlook of the unique insights thermal transport may offer to probe a much broader category of quantum phenomena.
Investigations of magnetically ordered phases on the femtosecond timescale have provided significant insights into the influence of charge and lattice degrees of freedom on the magnetic sub-system. However, short-range magnetic correlations occurring in the absence of long-range order, for example in spin-frustrated systems, are inaccessible to many ultrafast techniques. Here, we show how time-resolved resonant inelastic X-ray scattering (trRIXS) is capable of probing such short-ranged magnetic dynamics in a charge-transfer insulator through the detection of a Zhang-Rice singlet exciton. Utilizing trRIXS measurements at the O K-edge, and in combination with model calculations, we probe the short-range spin-correlations in the frustrated spin chain material CuGeO3 following photo-excitation, revealing a strong coupling between the local lattice and spin sub-systems.
Femtosecond (fs)-resolved simultaneous measurements of charge and spin dynamics reveal the coexistence of two different quasi-particle excitations in colossal magneto-resistive (CMR) manganites, with {em fs} and {em ps} relaxation times respectively. Their populations reverse size above a {em photoexcitation-intensity-threshold} coinciding with a sudden antiferro-to-ferromagnetic switching during $<$100 fs laser pulses. We present evidence that fast, metallic, mobile quasi--electrons dressed by {em quantum spin fluctuations} coexist with slow, localized, polaronic charge carriers in non-equilibrium phases. This may be central to CMR transition and leads to a laser-driven charge reorganization simultaneously with quantum fs magnetism via an emergent quantum-spin/charge/lattice transient coupling.
We show that the macroscopic magnetic and electronic properties of strongly correlated electron systems can be manipulated by coupling them to a cavity mode. As a paradigmatic example we consider the Fermi-Hubbard model and find that the electron-cavity coupling enhances the magnetic interaction between the electron spins in the ground-state manifold. At half filling this effect can be observed by a change in the magnetic susceptibility. At less than half filling, the cavity introduces a next-nearest neighbour hopping and mediates a long-range electron-electron interaction between distant sites. We study the ground state properties with Tensor Network methods and find that the cavity coupling can induce a new phase characterized by a momentum-space pairing effect for electrons.
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