arXiv subjects

Maurizio Monti

Publications and source records attributed to Maurizio Monti.

5 recordsLinked to original sources

arXiv2025

Ultrafast surface melting of orbital order in La0.5Sr1.5MnO4

Understanding how light modifies long-range order in quantum materials is key to improving our ability to control functionality. However, this is challenging if the response is heterogeneous. Here we address the most common form of light-induced heterogeneity, surface melting, and measure the dynamics of orbital order in the layered manganite, La0.5Sr1.5MnO4. We isolate the surface dynamics from the bulk by measuring the orbital truncation rod as well as orbital Bragg peak. After photoexcitation, the orbital Bragg peak shows an unusual narrowing, which suggests an increase in the correlation length in the probed volume. In contrast, the correlation length at the surface decreases. These differences can be reconciled if the material is heterogeneous, and light melts a less ordered surface. By isolating the surface response, we determine that the loss of long-range order is an incoherent process, which is likely accompanied by the formation of local polarons.

cond-mat.str-el↗

arXiv2025

Electron coherent phonon coupling in Pr$_{0.5}$Ca$_{1.5}$MnO$_4$ measured with ultrafast broadband spectroscopy

Photoexcitation of single-layered La$_{0.5}$Mn$_{1.5}$MnO$_4$ has played a key role in understanding orbital ordering and non-thermal states in the manganites. However, while orbital ordering in La$_{0.5}$Sr$_{1.5}$MnO$_4$ breaks the in-plane C$_4$ symmetry, many layered manganites show much more complex phase diagrams in which orbital ordering emerges from an already symmetry-broken high-temperature phase and also exhibit additional low-temperature phases. In this work, we examine the role of these phases 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 non-equilibrium state is sensitive to all phases. In particular, we deduce that coherent phonons modulate unoccupied electronic states that are sensitive to the different phases of the material. This gives rise to a non-linear scaling of the phonon signal with pump fluence at specific probe wavelengths.

cond-mat.str-el↗

arXiv2023

Determination and correction of spectral phase from principal component analysis of coherent phonons

Measuring the spectral phase of a pulse is key for performing wavelength resolved ultrafast measurements in the few femtosecond regime. However, accurate measurements in real experimental conditions can be challenging. We show that the reflectivity change induced by coherent phonons in a quantum material can be used to infer the spectral phase of an optical probe pulse with few-femtosecond accuracy.

physics.optics↗

arXiv2022

Non-thermal breaking of magnetic order via photo-generated spin defects

In Mott insulators the evolution of antiferromagnetic order to superconducting or charge-density-wave-like states upon chemical doping underpins the control of quantum phases. Photo-doping can induce similar transitions on the ultrafast timescale, however the response of the spin system has remained elusive. Here, we use 4D-ultrafast optical spectroscopy to extract quantitative magnetic dynamics in the spin-orbit coupled Mott insulator Sr3Ir2O7. We demonstrate that light can non-thermally melt long-range spin order. At low fluences magnetic order recovers within 1 ps despite demagnetization of roughly 50%. However, high fluences induce a crossover to a long-lived demagnetized state without increasing the lattice temperature. We show that the generation of photo-induced spin defects enables a mechanism that stabilizes the demagnetized state which could help expose new transient phases.

cond-mat.str-el↗

arXiv2021

Hot electron cooling in InSb probed by ultrafast time-resolved terahertz cyclotron resonance

Measuring terahertz (THz) conductivity on an ultrafast time scale is an excellent way to observe charge-carrier dynamics in semiconductors as a function of time after photoexcitation. However, a conductivity measurement alone cannot separate the effects of charge-carrier recombination from effective mass changes as charges cool and experience different regions of the electronic band structure. Here we present a form of time-resolved magneto-THz spectroscopy which allows us to measure cyclotron effective mass on a picosecond time scale. We demonstrate this technique by observing electron cooling in the technologically-significant narrow-bandgap semiconductor indium antimonide (InSb). A significant reduction of electron effective mass from 0.032$m_\mathrm{e}$ to 0.017$m_\mathrm{e}$ is observed in the first 200ps after injecting hot electrons. Measurement of electron effective mass in InSb as a function of photo-injected electron density agrees well with conduction band non-parabolicity predictions from ab initio calculations of the quasiparticle band structure.

cond-mat.mtrl-sci↗