arXiv subjects

Martina Basini

Publications and source records attributed to Martina Basini.

6 recordsLinked to original sources

arXiv2026

Quantifying angular momentum of coherently driven circular phonons

The use of intense terahertz (THz) pulses to manipulate low-energy excitations offers a powerful approach for ultrafast control of electronic and magnetic properties in materials. Theory suggests that circular ionic motions driven by THz fields carry angular momentum, potentially generating internal magnetic fields. Recent experiments in nonmagnetic SrTiO3 (STO) have hinted at such THz-induced fields, but their origin remains debated. Here, we employ ultrafast x-ray diffraction to resolve the time-dependent ionic trajectories in STO following excitation by circularly polarized THz pulses. Our analysis reveals that oxygen ions, despite their lower mass, contribute around 90% of the phonon angular momentum. The resulting imbalance between the negatively and positively charged ions provides a clear explanation for the mechanism behind induced magnetism in STO. This work further provides the first quantitative measurement of circular ionic motions and their angular momentum and establishes a general methodology for the investigation of angular momentum transfer in solids, paving the way for new strategies to control topological phonon transport and phonon-driven magnetism in quantum materials.

cond-mat.mtrl-sci↗

arXiv2026

THz-induced phonon mode mixing and collective dynamics in a polar nanolattice

Manipulating phonons through symmetry is a fundamental approach to alter the dynamic responses of materials. Most often new phases are sought through control of the unit-cell (e.g. via strain, doping, light, etc.). By comparison, there is vast potential to look beyond the unit-cell into higher-order architectures to control wave scattering and interference effects that remains less explored. We describe the THz-induced dynamics of an SrTiO$_{3}$ thin film with a nanoscale ordered interfacial dislocation network probed with 2- and 3-dimensional time-resolved x-ray diffraction and classical molecular dynamics simulations. We find that symmetry breaking at all scales is an effective approach to create a dynamical electric polarization and to control phonon mixing that generates previously unreported collective modes in the THz regime with circular vortex-like displacements. This work opens a new pathway to explore dynamical functional properties that can be extended to magnetic, electric, and ferroelectric systems by controlling the real-space topology via epitaxy.

cond-mat.str-el↗

arXiv2026

Anharmonic phonon coupling enabled by local inversion symmetry breaking at domain walls in ferroelastics

In ferroelastic materials, spontaneous symmetry breaking leads to the formation of twin domains. Although the bulk crystal typically remains centrosymmetric, inversion symmetry can be locally broken at the domain walls, potentially changing phonon selection rules and enabling local anharmonic phonon coupling. Here we report direct evidence of such anharmonic coupling in ferroelastic LaAlO$_3$ using two-dimensional Raman-terahertz spectroscopy. We attribute the cross-peaks observed in the two-dimensional spectra to both mechanical and electrical anharmonicity between the $A_{1g}$ Raman-active phonon and the $E_g$ phonon, which acquires finite infrared activity through local inversion symmetry breaking at ferroelastic domain walls. These findings provide new insight into the complex lattice dynamics of ferroelastic materials and highlight the potential of two-dimensional Raman-terahertz spectroscopy to uncover subtle symmetry breaking through the detection of intrinsically weak anharmonic signals.

cond-mat.mtrl-sci↗

arXiv2026

Uniaxial strain-driven ferroelastic domain control in LaAlO3

Multiferroic domain walls in functional oxides exhibit properties distinct from the bulk and are increasingly exploited as active elements in nanoelectronic and photonic devices. Deterministic control of domain populations has typically remained limited to local control, or removal with temperature. Here we demonstrate continuous, reversible manipulation of the ferroelastic domain structure in single-crystal LaAlO$_3$ using in-situ uniaxial strain. Combining atomic force microscopy, X-ray diffraction, and Raman spectroscopy with first-principles calculations we map the complete microscopic evolution of the twin domain population through the strain-driven transition from the rhombohedral $R\bar{3}c$ ground state toward the predicted orthorhombic $Fmmm$ phase. Applied strains below $0.5\%$ produce pronounced surface flattening and large-scale domain reorganisation, establishing uniaxial strain as a technically accessible control parameter for ferroelastic domain engineering. These results open a route to active, real-time programming of domain architectures in LaAlO$_3$-based heterostructures, with implications for strain-tunable superconducting interfaces, nanoscale phonon-polariton optics, and ultrafast lattice control.

cond-mat.mtrl-sci↗

arXiv2022

Terahertz ionic Kerr effect: Two-phonon contribution to the nonlinear optical response in insulators

The THz Kerr effect measures the birefringence induced in an otherwise isotropic material by a strong THz pulse driving the Raman-active excitations of the systems. Here we provide experimental evidence of a sizable Kerr response in insulating SrTiO3 due to infrared-active lattice vibrations. Such a signal, named ionic Kerr effect, is associated with the simultaneous excitation of multiple phonons. Thanks to a theoretical modeling of the time, polarization and temperature dependence of the birefringence we can disentangle the ionic Kerr effect from the off-resonant electronic excitations, providing an alternative tunable mechanism to modulate the refractive index on ultrashort time-scales via infra-red active phonons.

cond-mat.mtrl-sci↗

arXiv2018

R1 dispersion contrast at high field with fast field-cycling MRI

Contrast agents with a strong $R_1$ dispersion have been shown to be effective in generating target-specific contrast in MRI. The utilization of this $R_1$ field dependence requires the adaptation of a MRI scanner for fast field-cycling (FFC). Here, we present the first implementation and validation of FFC-MRI at a clinical field strength of 3 T. A field-cycling range of $\pm$100 mT around the nominal $B_0$ field was realized by inserting an additional insert coil into an otherwise conventional MRI system. System validation was successfully performed with selected iron oxide magnetic nanoparticles and comparison to FFC-NMR relaxometry measurements. Furthermore, we show proof-of-principle $R_1$ dispersion imaging and demonstrate the capability of generating R1 dispersion contrast at high field with suppressed background signal. With the presented ready-to-use hardware setup it is possible to investigate MRI contrast agents with a strong R1 dispersion at a field strength of 3 T.

physics.med-ph↗