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Arnau Romaguera

Publications and source records attributed to Arnau Romaguera.

6 recordsLinked to original sources

Coherent spin waves in a maximal entropy phase

In solids, disorder is conventionally regarded as detrimental to coherence. It typically localizes and dampens collective excitations, as exemplified by Anderson localization or the broadening of magnetic modes in systems lacking long-range order. While high-entropy materials are specifically designed to harness disorder and stabilize homogeneous mixed-phase structures that can display unique properties, this same disorder is nonetheless expected to preclude the formation of coherent magnetic excitations. To test the limits of this picture, we selected the antiferromagnetic system YBaCuFeO5, as it features two distinct transition metal atoms with significantly different magnetic moments, rendering its spin dynamics exceptionally sensitive to local atomic ordering. Combining resonant inelastic x-ray scattering and linear spin wave theory, we reveal a surprising paradox: YBaCuFeO5 exhibits an unexpected, entropy-driven mixed phase, in which disorder, rather than reducing the lifetime of the collective excitations, favors coherence. In this mixed phase, the spin waves remain dispersive, markedly distinct from those expected for an ordered ground state, and exhibit well-defined acoustic and optical branches separated by a large optical gap. These results demonstrate that in entropy-stabilized magnets, disorder can favor coherent collective modes previously thought to be exclusive to low-entropy systems.

cond-mat.str-el↗

Hierarchical quasiparticle dynamics in antiferromagnets revealed by time- and momentum-resolved X-ray scattering

Energy flows among coupled subsystems are essential for ultrafast dynamics and high-speed technologies. In magnetic materials, spin fluctuations -- magnons -- mediate these flows in ultrafast magnetism. Yet momentum-resolved access to low-energy magnons governing the microscopic dynamics has been lacking. Using time-resolved resonant diffuse scattering alongside complementary time-resolved X-ray techniques and quantum-kinetic simulations, we unveil the hierarchical energy pathways among correlated systems in the photoexcited antiferromagnet CuO. Above-bandgap excitation triggers near-instantaneous spin disorder, generating non-thermal magnons throughout reciprocal space within femtoseconds. Real-time momentum-resolved tracking reveals picosecond magnon quasi-thermalization, followed by nanosecond recovery via momentum-selective magnon-phonon scattering. The quasiparticle dispersion mismatch creates recovery bottlenecks that control non-equilibrium lifetimes. This microscopic framework transcends phenomenological models and generalizes across materials, establishing design principles for ultrafast control of material properties.

cond-mat.str-el↗

A light-induced charge order mode in a metastable cuprate ladder

We report the observation of an emergent charge order mode in the optically-excited cuprate ladder Sr$_{14}$Cu$_{24}$O$_{41}$. Near-infrared light in the ladder plane drives a symmetry-protected electronic metastable state together with a partial melting of the equilibrium charge order. Our time-resolved resonant inelastic x-ray scattering measurements at the upper Hubbard band reveal a gapless collective excitation dispersing from the charge-order wavevector up to 0.8 eV with a slope on the order of the quasiparticle velocity. These findings reveal a regime where correlated carriers acquire itinerant character at finite momentum, and charge order becomes dynamically fluctuating, offering a platform to explore light-induced pairing instabilities.

cond-mat.str-el↗

Symmetry-protected electronic metastability in an optically driven cuprate ladder

Optically excited quantum materials exhibit nonequilibrium states with remarkable emergent properties, but these phenomena are usually transient, decaying on picosecond timescales and limiting practical applications. Advancing the design and control of nonequilibrium phases requires the development of targeted strategies to achieve long-lived, metastable phases. Here, we report the discovery of symmetry-protected electronic metastability in the model cuprate ladder Sr$_{14}$Cu$_{24}$O$_{41}$. Using femtosecond resonant x-ray scattering and spectroscopy, we show that this metastability is driven by a transfer of holes from chain-like charge reservoirs into the ladders. This ultrafast charge redistribution arises from the optical dressing and activation of a hopping pathway that is forbidden by symmetry at equilibrium. Relaxation back to the ground state is hence suppressed after the pump coherence dissipates. Our findings highlight how dressing materials with electromagnetic fields can dynamically activate terms in the electronic Hamiltonian, and provide a rational design strategy for nonequilibrium phases of matter.

cond-mat.str-el↗

Magnetic properties of a highly ordered single crystal of the layered perovskite YBaCuFe$_{0.95}$Mn$_{0.05}$O$_5$

The layered perovskite YBaCuFeO5 (YBCFO) is able to adopt chiral magnetic order up to unexpectedly high temperatures, paving the way to strong magnetoelectric coupling at room temperature. In this perovskite A-site cations are fully ordered whereas the occupancy of the B-sites strongly depend on the preparation process. Though the structure is not geometrically frustrated, the presence of partial Fe3+/Cu2+ disorder at the B-sites produces magnetic frustration. In an effort to increase the spin-orbit coupling in the system, we have synthesized and studied YBaCuFe0.95Mn0.05O5 in single crystal form, where the highly symmetric Fe3+ ions (3d5) are partially substituted with Jahn-Teller active 3d4 Mn3+ ions. We report the structural and magnetic properties of a highly ordered single crystal of this layered perovskite, which are presented in comparison with a polycrystalline specimen (three times more disordered). Single-crystal neutron diffraction measurements reveal two collinear magnetic phases and the lack of incommensurate spiral order. The magnetic phases and transitions found in the crystal grown by the traveling solvent floating zone (TSFZ) method are fully described and analyzed in the light of its high level of Fe/Cu cationic order (~90%).

cond-mat.mtrl-sci↗

Ferromagnetic metallic Sr-rich Ln$_{1/2}$A$_{1/2}$CoO$_3$ cobaltites with spontaneous spin rotation

The Pr$_{0.50}$Sr$_{0.5}$0CoO$_3$ perovskite exhibits unique magnetostructural properties among the rest of ferromagnetic/metallic Ln$_{0.50}$Sr$_{0.50}$CoO$_3$ compounds. The sudden orthorhombic-tetragonal (Imma $\to$ I4/mcm) structural transition produces an unusual magnetic behavior versus temperature and external magnetic fields. In particular, the symmetry change is responsible for a spontaneous spin rotation in this metallic oxide. We have studied half-doped Ln$_{0.50}$(Sr$_{1-x}$A$_x$)$_{0.50}$CoO$_3$ cobaltites varying the ionic radius rA of A-site cations (divalent cations and lanthanides) in order to complete the T-rA phase diagram. The influence of the structural distortion and the A-cations size for the occurrence of a spontaneous spin reorientation in the metallic state has been investigated. As the reorientation of the magnetization is driven by the temperature induced collapse of the orthorhombic distortion, a careful investigation of the structural symmetry is presented varying the structural distortion of the Sr-rich half-doped cobaltites by means of both compositional and temperature changes. The region in the phase diagram of these perovskites where the phase of magnetic symmetry Fm'm'm replaces that of Im'm'a symmetry was determined in this family of ferromagnetic/metallic cobaltites. In that region the magnetization direction has rotated 45 degrees within the a-b plane with respect to the second.

cond-mat.mtrl-sci↗