arXiv subjects

Mattia Angeli

Publications and source records attributed to Mattia Angeli.

7 recordsLinked to original sources

arXiv2023

Localization of light in three dimensions: a mobility edge in the imaginary axis in non-Hermitian Hamiltonians

Searching for Anderson localization of light in three dimensions has challenged experimental and theoretical research for the last decades. Here the problem is analyzed through large scale numerical simulations, using a radiative Hamiltonian i.e. a non-Hermitian long-range hopping Hamiltonian, well suited to model light-matter interaction in cold atomic clouds. Light interaction in atomic clouds is considered in presence of positional and diagonal disorder. Due to the interplay of disorder and cooperative effects (sub- and super-radiance) a novel type of localization transition is shown to emerge, differing in several aspects from standard localization transitions which occur along the real energy axis. The localization transition discussed here is characterized by a mobility edge along the imaginary energy axis of the eigenvalues which is mostly independent from the real energy value of the eigenmodes. Differently from usual mobility edges it separates extended states from hybrid localized states and it manifest itself in the large moments of the participation ratio of the eigenstates. Our prediction of a mobility edge in the imaginary axis, i.e. depending on the eigenmode lifetime, paves the way to achieve control both in the time and space domain of open quantum systems.

cond-mat.mes-hall↗

arXiv2023

Low-energy moiré phonons in twisted bilayer van der Waals heterostructures

We develop a low-energy continuum model for phonons in twisted moiré bilayers, based on a configuration-space approach. In this approach, interatomic force constants are obtained from density functional theory (DFT) calculations of untwisted bilayers with various in-plane shifts. This allows for efficient computation of phonon properties for any small twist angle, while maintaining DFT-level accuracy. Based on this framework, we show how the low-energy phonon modes, including interlayer shearing and layer-breathing modes, vary with the twist angle. As the twist angle decreases, the frequencies of the low-energy modes are reordered and the atomic displacement fields corresponding to phonon eigenmodes break translational symmetry, developing periodicity on the moiré length scale. We demonstrate the capabilities of our model by calculating the phonon properties of three specific structures: bilayer graphene, bilayer molybdenum disulfide (MoS$_2$), and molybdenum diselenide-tungsten diselenide (MoSe$_2$-WSe$_2$).

cond-mat.mes-hall↗

arXiv2023

Domain-dependent surface adhesion in twisted few-layer graphene: Platform for moiré-assisted chemistry

Twisted van der Waals multilayers are widely regarded as a rich platform to access novel electronic phases, thanks to the multiple degrees of freedom such as layer thickness and twist angle that allow control of their electronic and chemical properties. Here, we propose that the stacking domains that form naturally due to the relative twist between successive layers act as an additional "knob" for controlling the behavior of these systems, and report the emergence and engineering of stacking domain-dependent surface chemistry in twisted few-layer graphene. Using mid-infrared near-field optical microscopy and atomic force microscopy, we observe a selective adhesion of metallic nanoparticles and liquid water at the domains with rhombohedral stacking configurations of minimally twisted double bi- and tri-layer graphene. Furthermore, we demonstrate that the manipulation of nanoparticles located at certain stacking domains can locally reconfigure the moiré superlattice in their vicinity at the μm-scale. In addition, we report first-principles simulations of the energetics of adhesion of metal atoms and water molecules on the stacking domains in an attempt to elucidate the origin of the observed selective adhesion. Our findings establish a new approach to controlling moiré-assisted chemistry and nanoengineering.

cond-mat.mtrl-sci↗

arXiv2023

Pressure--enhanced fractional Chern insulators in moiré transition metal dichalcogenides along a magic line

We show that pressure applied to twisted WSe$_2$ can enhance the many-body gap and region of stability of a fractional Chern insulator at filling $ν= 1/3$. Our results are based on exact diagonalization of a continuum model, whose pressure-dependence is obtained through {\it ab initio} methods. We interpret our results in terms of a {\it magic line} in the pressure-{\it vs}-twist angle phase diagram: along the magic line, the bandwidth of the topmost moiré valence band is minimized while simultaneously its quantum geometry nearly resembles that of an ideal Chern band. We expect our results to generalize to other twisted transition metal dichalcogenide homobilayers.

cond-mat.str-el↗

arXiv2022

Twistronics of Janus transition metal dichalcogenide bilayers

Twisted multilayers of two-dimensional (2D) materials are an increasingly important platform for investigating quantum phases of matter, and in particular, strongly correlated electrons. The moiré pattern introduced by the relative twist between layers creates effective potentials of long-wavelength, leading to electron localization. However, in contrast to the abundance of 2D materials, few twisted heterostructures have been studied until now. Here we develop a first-principle continuum theory to study the electronic bands introduced by moire patterns of twisted Janus transition metal dichalcogenides (TMD) homo- and hetero-bilayers. The model includes lattice relaxation, stacking-dependent effective mass, and Rashba spin-orbit coupling. We then perform a high-throughput generation and characterization of DFT-extracted continuum models for more than a hundred possible combinations of materials and stackings. Our model predicts that the moiré physics and emergent symmetries depend on chemical composition, vertical layer orientation, and twist angle, so that the minibands wavefunctions can form triangular, honeycomb, and Kagome networks. Rashba spin-orbit effects, peculiar of these systems, can dominate the moiré bandwidth at small angles. Our work enables the detailed investigation of Janus twisted heterostructures, allowing the discovery and control of novel electronic phenomena.

cond-mat.mtrl-sci↗

arXiv2021

Modeling the effect of the vaccination campaign on the Covid-19 pandemic

Population-wide vaccination is critical for containing the SARS-CoV-2 (Covid-19) pandemic when combined with restrictive and prevention measures. In this study, we introduce SAIVR, a mathematical model able to forecast the Covid-19 epidemic evolution during the vaccination campaign. SAIVR extends the widely used Susceptible-Infectious-Removed (SIR) model by considering the Asymptomatic (A) and Vaccinated (V) compartments. The model contains several parameters and initial conditions that are estimated by employing a semi-supervised machine learning procedure. After training an unsupervised neural network to solve the SAIVR differential equations, a supervised framework then estimates the optimal conditions and parameters that best fit recent infectious curves of 27 countries. Instructed by these results, we performed an extensive study on the temporal evolution of the pandemic under varying values of roll-out daily rates, vaccine efficacy, and a broad range of societal vaccine hesitancy/denial levels. The concept of herd immunity is questioned by studying future scenarios which involve different vaccination efforts and more infectious Covid-19 variants.

q-bio.PE↗

arXiv2018

Macroscopic coherence as an emergent property in molecular nanotubes

Nanotubular molecular self-aggregates are characterized by a high degree of symmetry and they are fundamental systems for light-harvesting and energy transport. While coherent effects are thought to be at the basis of their high efficiency, the relationship between structure, coherence and functionality is still an open problem. We analyze natural nanotubes present in Green Sulfur Bacteria. We show that they have the ability to support macroscopic coherent states, i.e. delocalized excitonic states coherently spread over many molecules, even at room temperature. Specifically, assuming a canonical thermal state, in natural structures we find a large thermal coherence length, of the order of 1000 molecules. By comparing natural structure with other mathematical models, we show that this macroscopic coherence cannot be explained either by the magnitude of the nearest-neighbour coupling between the molecules, which would induce a thermal coherence length of the order of 10 molecules, or by the presence of long-range interactions between the molecules. Indeed we prove that the existence of macroscopic coherent states is an emergent property of such structures due to the interplay between geometry and cooperativity (superradiance and super-transfer). In order to prove this, we give evidence that the lowest part of the spectrum of natural systems is determined by a cooperatively enhanced coupling (super-transfer) between the eigenstates of modular sub-units of the whole structure. Due to this enhanced coupling strength, the density of states is lowered close to the ground state, thus boosting the thermal coherence length.

cond-mat.mes-hall↗