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Daniel Pérez-Salinas

Publications and source records attributed to Daniel Pérez-Salinas.

2 recordsLinked to original sources

Orbital-lattice coupling and polaronic dressing of electronic states in Pr$_{0.5}$Ca$_{1.5}$MnO$_4$ revealed by ultrafast broadband spectroscopy

The interplay between long-range structural distortions and orbital order, and local short-range phenomena such as polarons, are key for understanding the properties of the manganites. In this work, we examine the role of local and long-range physics in relation to orbital ordering in the single-layered manganite Pr$_{0.5}$Ca$_{1.5}$MnO$_4$ with a combination of optical reflection anisotropy and ultrafast broadband pump-probe spectroscopy. We find that the reflection anisotropy, measured in equilibrium, is strongly sensitive to charge and orbital-ordering transition only. However, the ultrafast response, measuring the nonequilibrium state, is sensitive to a range of phenomena in the material, including delocalized (long wavelength) phonons as well as localized polarons. In particular, we find that a strong sensitivity to electronic and structural changes give rise to apparent nonlinearities when probed at specific wavelengths, despite the key degrees of freedom remaining linear. These observations point to the important role of orbital-lattice couplings and polarons dressing the electronic states across the Pr$_{0.5}$Ca$_{1.5}$MnO$_4$ phase diagram.

cond-mat.str-el↗

Ultrafast X-ray imaging of the light-induced phase transition in VO2

Using light to control transient phases in quantum materials is an emerging route to engineer new properties and functionality, with both thermal and non-thermal phases observed out of equilibrium. Transient phases are expected to be heterogeneous, either through photo-generated domain growth or by generating topological defects, and this impacts the dynamics of the system. However, this nanoscale heterogeneity has not been directly observed. Here we use time- and spectrally resolved coherent X-ray imaging to track the prototypical light induced insulator-to-metal phase transition in vanadium dioxide on the nanoscale with femtosecond time resolution. We show that the early-time dynamics are independent of the initial spatial heterogeneity and observe a 200 fs switch to the metallic phase. A heterogeneous response emerges only after hundreds of picoseconds. Through spectroscopic imaging, we reveal that the transient metallic phase is a highly orthorhombically strained rutile metallic phase, an interpretation that is in contrast to those based on spatially averaged probes. Our results demonstrate the critical importance of spatially and spectrally resolved measurements for understanding and interpreting the transient phases of quantum materials.

cond-mat.str-el↗