arXiv subjects

Francesco Banfi

Publications and source records attributed to Francesco Banfi.

At least 19 recordsLinked to original sources

arXiv2026

Fundamental thermo-visco mechanical interactions governing the acoustic response of laser-excited nanoparticles

In this work, we investigate the thermoacoustic generation and propagation of spherical waves in a viscous fluid induced by a laser-heated spherical particle. Periodic laser excitation gives rise to two coupled mechanisms of acoustic emission. Heat transfer from the particle to the surrounding fluid produces periodic compressions and rarefactions, giving rise to the thermophone effect, while periodic thermal expansion of the solid particle modulates its radius and launches acoustic waves through a piston-like action, known as the mechanophone effect. The thermophone contribution dominates at low frequencies, whereas the mechanophone mechanism becomes more relevant at higher frequencies, with the crossover governed by the interfacial thermal resistance at the solid-fluid boundary. We investigate the effect of nanoparticle embedding fluid viscosity on acoustic wave propagation. Viscous dissipation has a significant impact on attenuation and substantially alters the acoustic penetration depth, thereby affecting the effectiveness of the signal transmission. Viscous damping plays a key role in the mechanophone effect, where hypersonic frequency waves are generated, notably by photoacoustic excitation with picosecond and subpicosecond laser pulses. We develop a theoretical model based on the coupled conservation equations of mass, momentum, and energy in both phases, explicitly accounting for thermal diffusion and viscous losses. The reciprocal coupling between thermal and acoustic fields is fully described, allowing us to quantify how frequency and fluid viscosity jointly control the penetration length of the generated acoustic waves in realistic media. Finally, we discuss the implications for theranostics, highlighting how ensembles of laser-activated particles embedded in biological tissue may be optimized for diagnostic and therapeutic applications.

physics.flu-dyn↗

arXiv2024

Ultrafast nano generation of acoustic waves in water via a single carbon nanotube

Generation of ultra high frequency acoustic waves in water is key to nano resolution sensing, acoustic imaging and theranostics. In this context water immersed carbon nanotubes (CNTs) may act as an ideal optoacoustic source, due to their nanometric radial dimensions, peculiar thermal properties and broad band optical absorption. The generation mechanism of acoustic waves in water, upon excitation of both a single-wall (SW) and a multi-wall (MW) CNT with laser pulses of temporal width ranging from 5 ns down to ps, is theoretically investigated via a multi-scale approach. We show that, depending on the combination of CNT size and laser pulse duration, the CNT can act as a thermophone or a mechanophone. As a thermophone, the CNT acts as a nanoheater for the surrounding water, which, upon thermal expansion, launches the pressure wave. As a mechanophone, the CNT acts as a nanopiston, its thermal expansion directly triggering the pressure wave in water. Activation of the mechanophone effect is sought to trigger few nanometers wavelength sound waves in water, matching the CNT acoustic frequencies. This is at variance with respect to the commonly addressed case of water-immersed single metallic nano-objects excited with ns laser pulses, where only the thermophone effect significantly contributes. The present findings might be of impact in fields ranging from nanoscale non-destructive testing to water dynamics at the meso- to nano-scale.

cond-mat.mes-hall↗

arXiv2024

Tuning photoacoustics with nanotransducers via Thermal Boundary Resistance and Laser Pulse Duration

The photoacoustic effect in liquids, generated by metal nanoparticles excited with short laser pulses, offers high contrast imaging and promising medical treatment techniques. Understanding the role of the thermal boundary resistance (TBR) and the laser pulse duration in the generation mechanism of acoustic waves is essential to implement efficient photoacoustic nanotransducers. This work theoretically investigates, for the paradigmatic case of water-immersed gold nanocylinders, the role of the TBR and of laser pulse duration in the competition between the launching mechanisms: the thermophone and the mechanophone. In the thermophone, the nanoparticle acts as a nanoheater and the wave is launched by water thermal expansion. In the mechanophone, the nanoparticle directly acts as a nanopiston. Specifically, for a gold-water interface, the thermophone prevails under ns light pulse irradiation, while the mechanophone dominates shortening the pulse to the 10 ps regime. For a graphene-functionalized gold-water interface, instead, the mechanophone dominates over the entire range of explored laser pulse durations. Results point to high-TBR, liquid-immersed nanoparticles as potentially efficient photoacoustic nanogenerators, with the advantage of keeping the liquid environment temperature unaltered.

cond-mat.mes-hall↗

arXiv2024

Impact of a $MoS_2$ monolayer on the nanoscale thermoelastic response of silicon heterostructures

Understanding the thermoelastic response of a nanostructure is crucial for the choice of materials and interfaces in electronic devices with improved and tailored transport properties, at the length scales of the present technology. Here we show how the deposition of a $MoS_2$ monolayer can strongly modify the nanoscale thermoelastic dynamics of silicon substrates close to their interface. We achieve this result by creating a transient grating with extreme ultraviolet light, using ultrashort free-electron laser pulses, whose $\approx$84 nm period is comparable to the size of elements typically used in nanodevices, such as electric contacts and nanowires. The thermoelastic response, featured by coherent acoustic waves and an incoherent relaxation, is tangibly modified by the presence of monolayer $MoS_2$. Namely, we observed a major reduction of the amplitude of the surface mode, which is almost suppressed, while the longitudinal mode is basically unperturbed, aside from a faster decay of the acoustic modulations. We interpret this behavior as a selective modification of the surface elasticity and we discuss the conditions to observe such effect, which might be of immediate relevance for the design of Si-based nanoscale devices.

cond-mat.mtrl-sci↗

arXiv2023

Coherent control of the orbital occupation driving the insulator-to-metal Mott transition in V$_2$O$_3$

Managing light-matter interactions on timescales faster than the loss of electronic coherence is key for achieving full quantum control of the final products in solid-solid transformations. In this work, we demonstrate coherent electronic control of the photoinduced insulator-to-metal transition in the prototypical Mott insulator V$_2$O$_3$. Selective excitation of a specific interband transition with two phase-locked light pulses manipulates the orbital occupation of the correlated bands in a way that depends on the coherent evolution of the photoinduced superposition of states. A comparison between experimental results and numerical solutions of the optical Bloch equations provides an electronic coherence time on the order of 5 fs. Temperature-dependent experiments suggest that the electronic coherence time is enhanced in the vicinity of the insulator-to-metal transition critical temperature, thus highlighting the role of fluctuations in determining the electronic coherence. These results open new routes to selectively switch the functionalities of quantum materials and coherently control solid-solid electronic transformations.

cond-mat.str-el↗

arXiv2023

Halide perovskite artificial solids as a new platform to simulate collective phenomena in doped Mott insulators

The development of Quantum Simulators, artificial platforms where the predictions of many-body theories of correlated quantum materials can be tested in a controllable and tunable way, is one of the main challenges of condensed matter physics. Here we introduce artificial lattices made of lead halide perovskite nanocubes as a new platform to simulate and investigate the physics of correlated quantum materials. The ultrafast optical injection of quantum confined excitons plays the role of doping in real materials. We show that, at large photo-doping, the exciton gas undergoes an excitonic Mott transition, which fully realizes the magnetic-field-driven insulator-to-metal transition described by the Hubbard model. At lower photo-doping, the long-range interactions drive the formation of a collective superradiant state, in which the phases of the excitons generated in each single perovskite nanocube are coherently locked. Our results demonstrate that time-resolved experiments span a parameter region of the Hubbard model in which long-range and phase-coherent orders emerge out of a doped Mott insulating phase. This physics is relevant for a broad class of phenomena, such as superconductivity and charge-density waves in correlated materials whose properties are captured by doped Hubbard models.

cond-mat.str-el↗

arXiv2022

Nanoscale self-organisation and metastable non-thermal metallicity in Mott insulators

Mott transitions in real materials are first order and almost always associated with lattice distortions, both features promoting the emergence of nanotextured phases. This nanoscale self-organization creates spatially inhomogeneous regions, which can host and protect transient non-thermal electronic and lattice states triggered by light excitation. Here, we combine time-resolved X-ray microscopy with a Landau-Ginzburg functional approach for calculating the strain and electronic real-space configurations. We investigate V$_2$O$_3$, the archetypal Mott insulator in which nanoscale self-organization already exists in the low-temperature monoclinic phase and strongly affects the transition towards the high-temperature corundum metallic phase. Our joint experimental-theoretical approach uncovers a remarkable out-of-equilibrium phenomenon: the photo-induced stabilisation of the long sought monoclinic metal phase, which is absent at equilibrium and in homogeneous materials, but emerges as a metastable state solely when light excitation is combined with the underlying nanotexture of the monoclinic lattice.

cond-mat.str-el↗

arXiv2021

Analytical model of the acoustic response of nanogranular films adhering on a substrate

A 1D mechanical model for nanogranular films, based on a structural interface, is here presented. The analytical dispersion relation for the frequency and lifetimes of the acoustics breathing modes is obtained in terms of the interface layer thickness and porosity. The model is successfully benchmarked both against 3D Finite Element Method simulations and experimental photoacoustic data on a paradigmatic system available from the literature. A simpler 1D model, based on an homogenized interface, is also presented and its limitations and pitfalls discussed at the light of the more sophisticated pillar model. The pillar model captures the relevant physics responsible for acoustic dissipation at a disordered interface. Furthermore, the present findings furnish to the experimentalist an easy-to-adopt, benchmarked analytical tool to extract the interface layer physical parameters upon fitting of the acoustic data. The model is scale invariant and may be deployed, other than the case of granular materials, where a patched interface is involved.

physics.app-ph↗

arXiv2021

Non-thermal light-assisted resistance collapse in a V$_2$O$_3$-based Mott-insulator device

The insulator-to-metal transition in Mott insulators is the key mechanism for a novel class of electronic devices, belonging to the Mottronics family. Intense research efforts are currently devoted to the development of specific control protocols, usually based on the application of voltage, strain, pressure and light excitation. The ultimate goal is to achieve the complete control of the electronic phase transformation, with dramatic impact on the performance, for example, of resistive switching devices. Here, we investigate the simultaneous effect of external voltage and excitation by ultrashort light pulses on a single Mottronic device based on a V$_2$O$_3$ epitaxial thin film. The experimental results, supported by finite-element simulations of the thermal problem, demonstrate that the combination of light excitation and external electrical bias drives a volatile resistivity drop which goes beyond the combined effect of laser and Joule heating. Our results impact on the development of protocols for the non-thermal control of the resistive switching transition in correlated materials.

cond-mat.str-el↗

arXiv2021

Time-resolved thermal lens spectroscopy of glassy dynamics in supercooled liquids: theory and experiments

Specific heat and linear thermal expansivity are fundamental thermal dynamics and have been proven as interesting relaxing quantities to investigate in glass transition and glassy state. However, their possibility has much less been exploited compared to mechanical and dielectric susceptibilities due to the limited spectroscopy bandwidth. This work reports on simultaneous spectroscopy of the two by making use of ultrafast time-resolved thermal lens (TL) spectroscopy. Detailed modeling of the thermoelastic transients of a relaxing system subjected to ultrashort laser heating is presented to describe the TL response. The model has been applied to analyze a set of experimentally recorded TL waveforms, allowing the determination of relaxation strength and relaxation frequency from sub-kilohertz to sub-100 MHz and in a wide temperature range from 200-280 K.

cond-mat.soft↗

arXiv2021

Impulsive stimulated scatttering signal in supercooled liquids with Debye or Havriliak-Negami relaxation of the specific heat capacity and thermal expansion coefficient

A generalized physical model is introduced to describe the impulsive stimulated scattering (ISS) response of relaxing systems to photothermal excitation in a periodical grating geometry. The proposed approach starts from Debye and Havriliak-Negami expressions for both the frequency-dependent heat capacity, C(ω), and thermal expansion coefficient, γ(ω). Simulations are carried out on glycerol to test and compare the developed models with the existing semi-empirical model [1]. Debye behavior of the specific heat capacity is shown to be compatible with a two-temperature scenario, in which, in addition to the classical, experimentally observable temperature that characterizes the distribution of the system over vibrational energy states, a second temperature characterizes the state of the configurational energy landscape. The models here developed have been applied for the interpretation of the experimental ISS signals of supercooled glycerol, illustrating simultaneous and separate assessment of C(ω) and γ(ω) up to sub-100 MHz from thermoelastic transients.

cond-mat.soft↗

arXiv2021

Thermal dynamics and electronic temperature waves in layered correlated materials

We explore layered strongly correlated materials as a platform to identify and control unconventional heat transfer phenomena. We demonstrate that these systems can be tailored to sustain a wide spectrum of heat transport regimes, ranging from ballistic, to hydrodynamic all the way to diffusive. Within the hydrodynamic regime, wave-like temperature oscillations are predicted up to room temperature. All the above phenomena have a purely electronic origin, stemming from the existence of two components in the electronic system, each one thermalized at different temperatures. The interaction strength can be exploited as a knob to control the different thermal transport regimes. The present results pave the way to transition-metal oxide heterostructures as building blocks for nanodevices exploiting the wave-like nature of heat transfer on the picosecond time scale.

cond-mat.str-el↗

arXiv2020

Temperonic Crystal: a superlattice for temperature waves in graphene

The temperonic crystal, a periodic structure with a unit cell made of two slabs sustaining temperature wave-like oscillations on short time-scales, is introduced. The complex-valued dispersion relation for the temperature scalar field is investigated for the case of a localised temperature pulse. The dispersion discloses frequency gaps, tunable upon varying the slabs thermal properties. Results are shown for the paradigmatic case of a graphene-based temperonic crystal. The temperonic crystal extends the concept of superlattices to the realm of temperature waves, allowing for coherent control of ultrafast temperature pulses in the hydrodynamic regime at above liquid nitrogen temperatures.

cond-mat.mes-hall↗

arXiv2020

Tuning the Ultrafast Response of Fano Resonances in Halide Perovskite Nanoparticles

The full control of the fundamental photophysics of nanosystems at frequencies as high as few THz is key for tunable and ultrafast nano-photonic devices and metamaterials. Here we combine geometrical and ultrafast control of the optical properties of halide perovskite nanoparticles, which constitute a prominent platform for nanophotonics. The pulsed photoinjection of free carriers across the semiconducting gap leads to a sub-picosecond modification of the far-field electromagnetic properties that is fully controlled by the geometry of the system. When the nanoparticle size is tuned so as to achieve the overlap between the narrowband excitons and the geometry-controlled Mie resonances, the ultrafast modulation of the transmittivity is completely reversed with respect to what is usually observed in nanoparticles with different sizes, in bulk systems and in thin films. The interplay between chemical, geometrical and ultrafast tuning offers an additional control parameter with impact on nano-antennas and ultrafast optical switches.

cond-mat.mtrl-sci↗

arXiv2019

Accessing temperature waves: a dispersion relation perspective

In order to account for non-Fourier heat transport, occurring on short time and length scales, the often-praised Dual-Phase-Lag (DPL) model was conceived, introducing a causality relation between the onset of heat flux and the temperature gradient. The most prominent aspect of the first-order DPL model is the prediction of wave-like temperature propagation, the detection of which still remains elusive. Among the challenges to make further progress is the capability to disentangle the intertwining of the parameters affecting wave-like behaviour. This work contributes to the quest, providing a straightforward, easy-to-adopt, analytical mean to inspect the optimal conditions to observe temperature wave oscillations. The complex-valued dispersion relation for the temperature scalar field is investigated for the case of a localised temperature pulse in space, and for the case of a forced temperature oscillation in time. A modal quality factor is introduced showing that, for the case of the temperature gradient preceding the heat flux, the material acts as a bandpass filter for the temperature wave. The bandpass filter characteristics are accessed in terms of the relevant delay times entering the DPL model. The optimal region in parameters space is discussed in a variety of systems, covering nine and twelve decades in space and time-scale respectively. The here presented approach is of interest for the design of nanoscale thermal devices operating on ultra-fast and ultra-short time scales, a scenario here addressed for the case of quantum materials and graphite.

cond-mat.mes-hall↗

arXiv2019

Early-stage dynamics of metallic droplets embedded in the nanotextured Mott insulating phase of V$_2$O$_3$

Unveiling the physics that governs the intertwining between the nanoscale self-organization and the dynamics of insulator-to-metal transitions (\textit{IMT}) is key for controlling on demand the ultrafast switching in strongly correlated materials and nano-devices. A paradigmatic case is the \textit{IMT} in V$_2$O$_3$, for which the mechanism that leads to the nucleation and growth of metallic nano-droplets out of the supposedly homogeneous Mott insulating phase is still a mystery. Here, we combine X-ray photoemission electron microscopy and ultrafast non-equilibrium optical spectroscopy to investigate the early stage dynamics of isolated metallic nano-droplets across the \textit{IMT} in V$_2$O$_3$ thin films. Our experiments show that the low-temperature monoclinic antiferromagnetic insulating phase is characterized by the spontaneous formation of striped polydomains, with different lattice distortions. The insulating domain boundaries accommodate the birth of metallic nano-droplets, whose non-equilibrium expansion can be triggered by the photo-induced change of the 3$d$-orbital occupation. We address the relation between the spontaneous nanotexture of the Mott insulating phase in V$_2$O$_3$ and the timescale of the metallic seeds growth. We speculate that the photoinduced metallic growth can proceed along a non-thermal pathway in which the monoclinic lattice symmetry of the insulating phase is partially retained.

cond-mat.str-el↗

arXiv2018

Photoacoustic Sensing of Trapped Fluids in Nanoporous Thin Films: Device Engineering and Sensing Scheme

Accessing fluid infiltration in nanogranular coatings is an outstanding challenge, of relevance for applications ranging from nanomedicine to catalysis. A sensing platform, allowing to quantify the amount of fluid infiltrated in a nanogranular ultrathin coating, with thickness in the 10 to 40 nm range, is here proposed and theoretically investigated by multiscale modelling. The scheme relies on impulsive photoacoustic excitation of hypersonic mechanical breathing modes in engineered gas-phase synthesised nanogranular metallic ultathin films and time-resolved acousto-optical read-out of the breathing modes frequency shift upon liquid infiltration. A superior sensitivity, exceeding 26x103 cm^2/g, is predicted upon equivalent areal mass loading of a few ng/mm^2. The capability of the present scheme to discriminate among different infiltration patterns is discussed. The platform is an ideal tool to investigate nano fluidics in granular materials and naturally serves as a distributed nanogetter coating, integrating fluid sensing capabilities. The proposed scheme is readily extendable to other nanoscale and mesoscale porous materials.

physics.app-ph↗

arXiv2018

Ultrafast orbital manipulation and Mott physics in multi-band correlated materials

Multiorbital correlated materials are often on the verge of multiple electronic phases (metallic, insulating, super- conducting, charge and orbitally ordered), which can be explored and controlled by small changes of the external parameters. The use of ultrashort light pulses as a mean to transiently modify the band population is leading to fundamentally new results. In this paper we will review recent advances in the field and we will discuss the pos- sibility of manipulating the orbital polarization in correlated multi-band solid state systems. This technique can provide new understanding of the ground state properties of many interesting classes of quantum materials and offers a new tool to induce transient emergent properties with no counterpart at equilibrium. We will address: the discovery of high-energy Mottness in superconducting copper oxides and its impact on our understanding of the cuprate phase diagram; the instability of the Mott insulating phase in photoexcited vanadium oxides; the manipulation of orbital-selective correlations in iron-based superconductors; the pumping of local electronic excitons and the consequent transient effective quasiparticle cooling in alkali-doped fullerides. Finally, we will discuss a novel route to manipulate the orbital polarization in a a k-resolved fashion.

cond-mat.str-el↗