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Davide Sangalli

Publications and source records attributed to Davide Sangalli.

At least 19 recordsLinked to original sources

Dark exciton signatures in the infrared transient absorption of MoS$_2$ monolayer

Dark excitons play a central role in the nonequilibrium dynamics of two-dimensional semiconductors, but remain difficult to characterize. Transient-absorption experiments, with probes tuned in exciton-exciton transitions energy range (exc-tr-abs), can detect excitations from any populated dark excitons, including symmetry-forbidden, spin-forbidden, and finite-momentum ones. In this work, we develop a $GW$+BSE scheme for computing exc-tr-abs spectra from arbitrary populated exciton distributions. These dark excitons are included equally by evaluating exciton-exciton dipoles in a locally smooth gauge, including intra- and inter-band contributions. For monolayer MoS$_2$, the exc-tr-abs signal arises from the $\Gamma$, $K$, $M$, and $Q$ valleys, differing substantially from the $\Gamma$-only interpretation. Exciton-exciton dipoles show similar intensities across these valleys, while their weights are dictated by initial excitonic populations. State- and spin-resolved analyses assign the peaks to $1s \rightarrow 2p$ and $1s \rightarrow 3p$ transitions from both spin-flip and spin-conserving A and B excitons across valleys and momenta.

cond-mat.mtrl-sci

Efficient nonequilibrium electron dynamics from first-principles: leveraging Koopmans spectral functionals and Wannier localization

We present an efficient first-principles approach for simulating the nonequilibrium electron dynamics in extended systems beyond the linear regime. The method combines Koopmans-compliant functionals, which provide an accurate quasiparticle band structures, with the real-time evolution of the electronic density matrix in a Wannier basis within the Hartree plus screened exchange (HSEX) approximation. The locality of the orbital basis enables physically motivated approximations that significantly reduce both the computational cost and memory requirements while preserving accuracy. The screened Coulomb interaction, the central ingredient of the HSEX self-energy, is computed efficiently using density-functional perturbation theory. We benchmark the approach in the linear regime against experimental spectra and reference Green's function calculations for systems featuring both weakly and strongly bound excitons. Moving to the nonlinear regime, we investigate high-harmonic generation (HHG) in silicon and lithium fluoride. While in silicon the HHG spectrum is largely governed by the quasiparticle band structure, in LiF, a material featuring strong excitonics effect, the harmonic emission is selectively enhanced at excitonic resonances, suggesting that HHG probes correlated electron-hole excitations rather than solely the quasiparticle band structure. The present framework enables fully \textit{ab-initio} simulations of excitonic effects in nonlinear optical spectra at a significantly reduced computational cost compared to real-time Green's function approaches, providing an efficient route to the study of ultrafast and strong-field phenomena in solids.

cond-mat.mtrl-sci

The Frequency-Dependent Spin Contribution to the Magnetoelectric Tensor of Cr$_2$O$_3$: A First-Principles Study

The magnetoelectric (ME) effect provides a promising pathway for controlling magnetic functionalities using electric fields. While first-principles methods for the static linear ME response are well established, comparable approaches for the frequency-dependent response remain less developed, despite experiments showing pronounced finite-frequency resonances. Here, we investigate the dynamical spin-induced linear ME response from first principles and systematically compare the independent-particle approximation (IPA), random-phase approximation (RPA), time-dependent density functional theory (TDDFT), and the Bethe-Salpeter equation (BSE). We apply these methods to the prototypical ME material Cr$_2$O$_3$ and compare the results with available experimental and theoretical studies. We find that the IPA and RPA fail to reproduce the previously reported finite static limit of the spin-induced response. Within the BSE framework, pronounced excitonic resonances emerge in the ME spectrum, in qualitative agreement with experiment. We also identify a magnon-like peak that coincides with a pole of the transverse spin susceptibility while remaining essentially dark in optical absorption, highlighting the sensitivity of the ME response to spin excitations. TDDFT places this mode closer to the expected low-energy magnonic regime and yields a sizable static spin-induced response. Our results show that these frameworks capture complementary aspects of the dynamical ME response. Low-energy collective spin excitations are required to recover the static limit, whereas electron-hole interactions are essential for reproducing the excitonic resonances.

cond-mat.mtrl-sci

Nonequilibrium dynamics of high energy transitions in monolayer WSe$_{2}$

High-energy optical transitions in monolayer transition-metal dichalcogenides exhibit characteristics that are markedly distinct from those of lower-lying band-edge excitons. These differences arise from the involvement of electronic states located at regions of the Brillouin zone that are displaced from the $K$ valleys. In this work, we investigate the ultrafast dynamics of these high-energy excitations by employing broadband ultrafast transient absorption spectroscopy spanning the visible to ultraviolet spectral range. We observe that the formation and relaxation dynamics of one of the high energy transitions display a distinct behavior compared to the lower-energy excitonic resonances, developing on a significantly slower timescale. First-principles calculations of the excitonic landscape allow us to account for this delayed response and attribute it to the phonon-mediated formation of momentum-dark excitons.

cond-mat.mtrl-sci

Coherent Ultrafast Excitonic Oscillations in Monolayer WS$_2$

Monolayer transition metal dichalcogenides are a suitable platform for studying excitonic coherence in the light-matter coupling regime. We present an ab initio time-dependent GW-Bethe-Salpeter equation (GW-BSE) investigation of coherent excitonic dynamics in monolayer WS$_2$. By solving the coherent coupling between the A, A$^{*}$, and B excitons under linearly polarized pump fields, we identify the microscopic origin of the resulting oscillatory dynamics and rationalize it using an effective theoretical model. Our results provide the interpretation of recently reported coherent excitonic phenomena in monolayer WS$_2$ (Nano Lett. 24, 8117 (2024)). Building on this first-principles time-resolved framework, we propose a tailored pump-probe scheme that enables the controlled generation and regeneration of coherent oscillations between excitonic states. These findings establish a predictive route for controlling excitonic coherence in two-dimensional materials, with direct relevance for ultrafast optoelectronic switches and solid-state quantum logic devices.

cond-mat.mtrl-sci

Symmetries of excitons

Excitons, bound electron-hole pairs, are responsible for strong optical resonances near the bandgap in low-dimensional materials and wide-bandgap insulators. Although current ab initio methods can accurately determine exciton energies and eigenstates, their symmetries have been much less explored. In this work, we employ standard group-theory methods to analyse the transformation properties of excitonic states, obtained by solving the BSE, under crystal symmetry operations. We develop an approach to assign irreducible-representation labels to excitonic states, providing a state-of-the-art framework for analysing their symmetries and selection rules (including, for example, the case of exciton-phonon coupling). Complementary to the symmetry classification, we introduce the concept of total crystal angular momentum for excitons in the presence of rotational symmetries, allowing the derivation of conservation laws. Furthermore, we demonstrate how these symmetry properties can be exploited to greatly enhance the computational efficiency of exciton calculations with the BSE. We apply our methodology to three prototypical systems to understand the role of symmetries in different contexts: (i) For LiF, we present the symmetry analysis of the entire excitonic dispersion and examine the selection rules for optical absorption. (ii) In the calculation of resonant Raman spectra of monolayer MoSe2, we demonstrate how the conservation of total crystal angular momentum governs exciton-phonon interactions, leading to the observed resonant enhancement. (iii) In bulk hBN, we analyze the role of symmetries for the coupling of finite-momentum excitons to finite-momentum phonons and their manifestation in the phonon-assisted luminescence spectra. This work establishes a general and robust framework for understanding the symmetry properties of excitons in crystals, providing a foundation for future studies.

cond-mat.mes-hall

Solvers for the Hermitian and the pseudo-Hermitian Bethe-Salpeter equation in the Yambo code: Implementation and Performance

We analyze the performance of two strategies in solving the structured eigenvalue problem deriving from the Bethe-Salpeter equation (BSE) in condensed matter physics. The BSE matrix is constructed with the Yambo code, and the two strategies are implemented by interfacing Yambo with the ScaLAPACK and ELPA libraries for direct diagonalization, and with the SLEPc library for the iterative approach. We consider both the Hermitian (Tamm-Dancoff approximation) and pseudo-Hermitian forms, addressing dense matrices of three different sizes. A description of the implementation is also provided, with details for the pseudo-Hermitian case. Timing and memory utilization are analyzed on both CPU and GPU clusters. Our results demonstrate that it is now feasible to handle dense BSE matrices of the order of 10^5.

cond-mat.mtrl-sci

Magnons in chromium trihalides from \emph{ab initio} Bethe-Salpeter equation

Chromium trihalides (CrX$_3$, with $\rm{X=I,Br,Cl}$) are layered ferromagnetic materials with rich physics and possible applications. Their structure consists of magnetic Cr atoms positioned between two layers of halide atoms. The choice of halide results in distinct magnetic properties, but their effect on spin-wave (magnon) excitations is not fully understood. Here we present first-principles calculations of magnon dispersions and wave functions for monolayer Cr trihalides using the finite-momentum Bethe-Salpeter equation (BSE) to describe collective spin-flip excitations. % We study the dependence of magnon dispersions on the halide species and resolve the small topological gap at the Dirac point in the magnon spectrum by including spin-orbit coupling. Analysis of magnon wave functions reveals that magnons are made up of electronic transitions with a wider energy range than excitons in CrX$_3$ monolayers, providing insight into magnon states in real and reciprocal space. We discuss Heisenberg exchange parameters extracted from the BSE and discuss the convergence of BSE magnon calculations. Our work advances the quantitative modeling of magnons in two-dimensional materials, providing the starting point for studying magnon interactions in a first-principles BSE framework.

cond-mat.mtrl-sci

Magnon-phonon interactions from first principles

Modeling spin-wave (magnon) dynamics in novel materials is important to advance spintronics and spin-based quantum technologies. The interactions between magnons and lattice vibrations (phonons) limit the length scale for magnon transport. However, quantifying these interactions remains challenging. Here we show many-body calculations of magnon-phonon (mag-ph) coupling based on the ab initio Bethe-Salpeter equation. We derive expressions for mag-ph coupling matrices and compute them in 2D ferromagnets, focusing on hydrogenated graphene and monolayer CrI3. Our analysis shows that electron-phonon (e-ph) and mag-ph interactions differ significantly, where modes with weak e-ph coupling can exhibit strong mag-ph coupling (and vice versa), and reveals which phonon modes couple more strongly with magnons. In both materials studied here, the inelastic magnon relaxation time is found to decrease abruptly above the threshold for emission of strongly coupled phonons, thereby defining a low-energy window for efficient magnon transport. By averaging in this window, we compute the temperature-dependent magnon mean-free path, a key figure of merit for spintronics, entirely from first principles. The theory and computational tools shown in this work enable studies of magnon interactions, scattering, and dynamics in generic materials, advancing the design of magnetic systems and magnon- and spin-based devices.

cond-mat.mtrl-sci

Detection of a coherent excitonic state in the layered semiconductor BiI$_{3}$

The measurement and manipulation of the coherent dynamics of excitonic states constitute a forefront research challenge in semiconductor optics and in quantum coherence-based protocols for optoelectronic technologies. Layered semiconductors have emerged as an ideal platform for the study of exciton dynamics with accessible and technologically relevant energy and time scales. Here, we investigate the sub-picosecond exciton dynamics in a van-der-Waals semiconductor upon quasi-resonant excitation, and achieve to single out an incipient coherent excitonic state. Combining broadband transient reflectance spectroscopy and simulations based on many-body perturbation theory, we reveal a transient enhancement of the excitonic line intensity that originates from the photoinduced coherent polarization that is phase-locked with the interacting electromagnetic field. This finding allows us to define the spectral signature of a coherent excitonic state and to experimentally track the dynamical crossover from coherent to incoherent exciton, unlocking the prospective optical control of an exciton population on the intrinsic quantum-coherence timescale.

cond-mat.mtrl-sci

The 2025 Roadmap to Ultrafast Dynamics: Frontiers of Theoretical and Computational Modelling

The exploration of ultrafast phenomena is a frontier of condensed matter research, where the interplay of theory, computation, and experiment is unveiling new opportunities for understanding and engineering quantum materials. With the advent of advanced experimental techniques and computational tools, it has become possible to probe and manipulate nonequilibrium processes at unprecedented temporal and spatial resolutions, providing insights into the dynamical behavior of matter under extreme conditions. These capabilities have the potential to revolutionize fields ranging from optoelectronics and quantum information to catalysis and energy storage. This Roadmap captures the collective progress and vision of leading researchers, addressing challenges and opportunities across key areas of ultrafast science. Contributions in this Roadmap span the development of ab initio methods for time-resolved spectroscopy, the dynamics of driven correlated systems, the engineering of materials in optical cavities, and the adoption of FAIR principles for data sharing and analysis. Together, these efforts highlight the interdisciplinary nature of ultrafast research and its reliance on cutting-edge methodologies, including quantum electrodynamical density-functional theory, correlated electronic structure methods, nonequilibrium Green's function approaches, quantum and ab initio simulations.

cond-mat.mtrl-sci

Unveiling exciton formation: exploring the early stages in time, energy and momentum domain

Resolving the early-stage dynamics of exciton formation following non-resonant photoexcitation in time, energy, and momentum is quite challenging due to their inherently fast timescales and the proximity of the excitonic state to the bottom of the conduction band. In this study, by combining time- and angle-resolved photoemission spectroscopy with \mathit{ab initio} numerical simulations, we capture the timing of the early-stage exciton dynamics in energy and momentum, starting from the photoexcited population in the conduction band, progressing through the formation of free excitons, and ultimately leading to their trapping in lattice deformations. The chosen material is bismuth tri-iodide ($BiI_3$), a layered semiconductor with a rich landscape of excitons in the electronic structure both in bulk and in monolayer form. The obtained results, providing a full characterization of the exciton formation, elucidate the early stages of the physical phenomena underlying the operation of the ultrafast semiconductor device.

cond-mat.mtrl-sci

Physics of excitons in layered BiI$_{3}$. Effects of dimensionality and crystal anisotropy

We carry out a detailed theoretical study of the electronic and optical properties of bulk and monolayer bismuth triiodide (BiI$_{3}$), a layered metal halide, using the ab initio GW+BSE scheme with a full spinorial formulation. We discuss in detail the effects due to the change of dimensionality and the role of spin-orbit coupling. Moreover, we compute the exciton dispersion by solving the BSE at finite momentum, also analysing transverse (TE) and longitudinal (LE) excitons, and the L-T splitting at $\bf{q}\approxΓ$. The results provide a reference for future experimental measurements. In addition, the interplay between spin-orbit coupling and large binding energy, together with the role of quantum confinement, confirm that BiI$_{3}$ is an interesting material for opto-electronic applications and show that it is a good candidate for the study of exciton dynamics.

cond-mat.mtrl-sci

First-principles study of luminescence in hexagonal boron nitride single layer: exciton-phonon coupling and the role of substrate

Hexagonal boron nitride (hBN) is a wide band gap material with both strong excitonic light emission in the ultraviolet and strong exciton-phonon coupling. Luminescence experiments performed on the recently synthesized monolayer form (m-hBN) present emission spectra that differ from one another, with some suggesting a coexistence between phonon-assisted and direct emission channels. Motivated by these results, we investigated the optical response of (m-hBN) using a new \textit{ab initio} approach that takes into account the effects of atomic vibrations on the luminescence spectra. We construct the dynamical exciton-phonon self-energy, then use it to perturbatively correct the optical response functions and test this approach on bulk hBN as a benchmark. Within our approach we are able to estimate the renormalisation of the direct peak induced by phonon-assisted transitions, and this allows us to accurately describe spectra where both processes are present. We found that the emission signal of m-hBN is strongly dependent on its interaction with the substrate, which changes its nature from direct to indirect material and modifies the screening felt by the electrons. We attribute the m-hBN emission signal to the bright direct excitons and consider the likelihood of phonon replicas appearing.

cond-mat.mtrl-sci

Strong Coupling of Coherent Phonons to Excitons in Semiconducting Monolayer MoTe$_2$

The coupling of the electron system to lattice vibrations and their time-dependent control and detection provides unique insight into the non-equilibrium physics of semiconductors. Here, we investigate the ultrafast transient response of semiconducting monolayer 2$H$-MoTe$_2$ encapsulated with $h$BN using broadband optical pump-probe microscopy. The sub-40-fs pump pulse triggers extremely intense and long-lived coherent oscillations in the spectral region of the A' and B' exciton resonances, up to $\sim$20% of the maximum transient signal, due to the displacive excitation of the out-of-plane $A_{1g}$ phonon. Ab-initio calculations reveal a dramatic rearrangement of the optical absorption of monolayer MoTe$_2$ induced by an out-of-plane stretching and compression of the crystal lattice, consistent with an $A_{1g}$-type oscillation. Our results highlight the extreme sensitivity of the optical properties of monolayer TMDs to small structural modifications and their manipulation with light.

cond-mat.mes-hall

Assignment of excitonic insulators in \textit{ab initio} theories: the case of NiBr$_2$

In this work we perform a detailed first-principles analysis of the electronic and optical properties of NiBr$_2$ within the state-of-the-art $GW$+BSE scheme to determine whether this system displays negative excitonic energies, which would identify it as an (half) excitonic insulator. Particular attention is payed to the convergence of the $GW$ band structure and to the consistency between approximations employed in the ground-state calculations and approximations employed in the linear response calculations. We show that these two issues play a crucial role in identifying the excitonic nature of NiBr$_2$.

cond-mat.mtrl-sci

Ab initio Circular Dichroism with the Yambo code: beyond the Independent Particle approximation

Circular dichroism (CD) spectroscopy is a useful technique for characterizing chiral molecules. It is more sensitive than total absorption to molecule conformation, and it is routinely used to identify enantiomers. We present here absorption and CD spectra within the Time Dependent (TD) B3LYP approximation in c-GlyPhe, a cyclo-dipeptide containing an aromatic group. Results from codes in localized basis-set (Orca and MolGW) are carefully compared with the novel TD-B3LYP implementation we developed in the Yambo code, that uses a plane-wave basis set.

physics.chem-ph

Ab initio Circular Dichroism with the Yambo code: applications to dipeptides

Circular dichroism (CD) spectroscopy is a useful technique for characterizing chiral molecules. It is more sensitive than total absorption to molecule conformation, and it is routinely used to identify enantiomers. We present here a first principles implementation of CD with application to three cyclo-dipeptides. Our CD approach for molecules has been integrated in the 5.0 release of the Yambo code [1], distributed under GPL.

physics.chem-ph