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Michele Diego

Publications and source records attributed to Michele Diego.

11 recordsLinked to original sources

Enhanced Near-Field Thermal Radiation Driven by Multiple Corner and Edge Modes in Subwavelength Square Nanowires

We demonstrate that the near-field thermal radiation between subwavelength SiC nanowires with square cross sections is dominated by multiple corner and edge resonances rather than the single surface-phonon-polariton channel of planar surfaces. Fluctuational electrodynamics simulations reveal that these resonances lie within the SiC Reststrahlen band, redshift for thinner nanowires, and yield a four-fold enhancement of thermal conductance. This maximum enhancement occurs when the separation gap nearly matches the nanowire thickness, balancing dimensional confinement and interwire coupling. These findings establish square nanowires as a versatile platform for geometrycontrolled near-field heat transfer in nanoscale heat management and energy conversion.

cond-mat.mes-hall

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

Gigahertz-frequency Lamb wave resonator cavities on suspended lithium niobate for quantum acoustics

Phononic nanodevices offer a promising route toward quantum technologies, as phonons combine strong confinement within matter with broad coupling capabilities to various quantum systems. In particular, the piezoelectric response of materials such as lithium niobate enables coupling between superconducting qubits and gigahertz-frequency phonons. However, bulk lithium niobate phononic devices typically rely on surface acoustic waves and are therefore inherently subject to leakage from the surface into the bulk substrate. Here, we explore the acoustic behavior of resonator cavities supporting GHz-frequency Lamb waves in a 200 nm-thick suspended lithium niobate layer. We characterize the acoustic response at both room and millikelvin temperatures. We find that our resonator cavities with strong confinement reach intrinsic quality factors of approximately 6000 at the single phonon level. We use the measured parameters of the resonators to model their coupling to a superconducting transmon qubit, allowing us to evaluate their potential as quantum acoustic devices.

cond-mat.mes-hall

Hypersonic acoustic wave control via hyperuniform phononic nanostructures

Controlling hypersonic surface acoustic waves is crucial for advanced phononic devices such as high-frequency filters, sensors, and quantum computing components. While periodic phononic crystals enable precise bandgap engineering, their ability to suppress acoustic waves is limited to specific frequency ranges. Here, we experimentally demonstrate the control of surface acoustic waves using a hyperuniform arrangement of gold nanopillars on a lithium niobate layer. The hyperuniform structure exhibits characteristics of both random and ordered systems, leading to an overall reduction in acoustic transmission and the formation of bandgap-like regions where phonon propagation is strongly suppressed. We further demonstrate effective waveguiding by incorporating linear and S-shaped waveguides into the hyperuniform pattern. Both simulations and experiments confirm high transmission through the waveguides at frequencies within the bandgaps, demonstrating the flexibility of hyperuniform structures to support waveguides of complex shapes. These findings provide a novel approach to overcoming the limitations of traditional phononic crystals and advancing acoustic technologies in applications such as mechanical quantum computing and smartphone filters.

cond-mat.mes-hall

Phonon dispersion of nanoscale honeycomb phononic crystal: gigahertz and terahertz spectroscopy comparison

Phonons-quantized vibrational modes in crystalline structures-govern phenomena ranging from thermal and mechanical transport to quantum mechanics. In recent years, a new class of artificial materials called phononic crystals has emerged, aiming to control phononic properties. These materials are created by introducing a superlattice structure on top of an already-existing atomic lattice. Typically, phononic crystals are described using a continuous model, in which effective elastic constants approximate potentials between atoms. This approximation, however, assumes the wavelengths of vibrations to be significantly greater than the interatomic distance. In this work, we experimentally investigate the behavior of a honeycomb silicon phononic crystal in the gigahertz range, where the continuum approximation holds, and in the terahertz range, where the phonon wavelengths are comparable to interatomic distances. Using Brillouin light scattering, we investigate the phonon dispersion of the phononic crystal in the gigahertz range, finding a close match with simulations based on the continuous model. Conversely, Raman spectroscopy reveals no difference between the phononic crystal, an unpatterned membrane, and a bulk silicon structure in the terahertz range, showing that the continuous model no longer holds at these higher frequencies.

cond-mat.mes-hall

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

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

Piezoelectrically driven diamond phononic nanocavity by phonon-matching scheme for quantum applications

Efficiently exciting and controlling phonons in diamond nanoresonators represents a fundamental challenge for quantum applications. Here, we theoretically demonstrate the possibility to excite mechanical modes within a double-hybrid-cavity (DHC), formed by adjoining to a diamond cavity a second cavity, made of aluminum nitride. The latter is piezoelectric and serves as a microwave-to-phonon transducer, activating mechanical modes in the entire DHC. We show the process to match the cavities phononic properties, making them work coordinately in the DHC and obtaining a well confined mode. In the diamond part of the cavity, this mode replicates the fundamental mode of the individual diamond cavity, showing that the piezoelectric transducer doesn't alter the diamond individual fundamental mode. In the piezoelectric part, the strong confinement of stress and electric field results in a high piezoelectric coupling rate, demonstrating the effectiveness of a phononic cavity as a transducer. The study is contextualized in the framework of a quantum networking application, where the DHC serves as a spin qubit, exploiting the spin-mechanical coupling within diamond color centers.

cond-mat.mes-hall

Non-equilibrium quantum domain reconfiguration dynamics in a two-dimensional electronic crystal: experiments and quantum simulations

Relaxation dynamics of complex many-body quantum systems brought out of equilibrium and subsequently trapped into metastable states is a very active field of research from both the theoretical and experimental point of view with implications in a wide array of topics from macroscopic quantum tunnelling and nucleosynthesis to non-equilibrium superconductivity and new energy-efficient memory devices. Understanding the dynamics of such systems is crucial for exploring fundamental aspects of many-body non-equilibrium quantum physics. In this work we investigate quantum domain reconfiguration dynamics in the electronic superlattice of a quantum material where classical dynamics is topologically constrained. The crossover from temperature to quantum fluctuation dominated dynamics in the context of environmental noise is investigated by directly observing charge reconfiguration with time-resolved scanning tunneling microscopy. The process is modelled using a programmable superconducting quantum simulator in which qubit interconnections correspond directly to the microscopic interactions between electrons in the quantum material. Crucially, the dynamics of both the experiment on the quantum material and the simulation is driven by spectrally similar pink noise. We find that the simulations reproduce the emergent time evolution and temperature dependence of the experimentally observed electronic domain dynamics remarkably well. The combined experiment and simulations lead to a better understanding of noise-driven quantum dynamics in open quantum systems. From a practical viewpoint, the results are important for understanding the origin of the retention time in non-volatile memory devices such as those based on 1T-TaS2.

quant-ph

Energy efficient manipulation of topologically protected states in non-volatile ultrafast charge configuration memory devices

Non-volatile magnetic storage, from 1940s magnetic core to present day racetrack memory and magnetic anisotropy switching devices rely on the metastability of magnetic domains to store information. However, the inherent inefficiency of converting the information-carrying charge current into magnetization switching sets fundamental limitations in energy consumption. Other non-magnetic non-volatile memories such as memristors, ferroelectric memory and phase change memory devices also rely on energetically relatively costly crystal structural rearrangements to store information. In contrast, conventional electronic charge states in quantum dots for example, can be switched in femtoseconds with high efficiency, but any stored information dissipates rapidly. Here we present a radically different approach in the form of a charge-configuration memory (CCM) device that relies on charge-injection-driven electronic crystal melting and topological protection of the resulting electronic domain configurations of a two-dimensional electronic crystal to store information. With multiprobe scanning tunneling microscopy (STM) we show microscopically, within an operational device, how dislocations in the domain ordering lead to metastability by a mechanism that is topologically equivalent to magnetic bubble memory. The devices have a very small switching energy (<2.2 fJ/bit), ultrafast switching speed of <11 ps and operational range over more than 3 orders of magnitude in temperature (<250 mK ~ 190 K). Together with their simple functionality, a large resistance switching ratio, straightforward fabrication and impressive endurance, CCM devices introduce a new memory paradigm in emerging cryo-computing and other high-performance computing applications that require ultrahigh speed and low energy consumption.

cond-mat.str-el

A time-domain phase diagram of metastable states in a charge ordered quantum material

Metastable self-organized electronic states in quantum materials are of fundamental importance, displaying emergent dynamical properties that may be used in new generations of sensors and memory devices. Such states are typically formed through phase transitions under non-equilibrium conditions and the final state is reached through processes that span a large range of timescales. By using time-resolved optical techniques and femtosecond-pulse-excited scanning tunneling microscopy (STM), the evolution of the metastable states in the quasi-two-dimensional dichalcogenide 1T-TaS2 is mapped out on a temporal phase diagram using the photon density and temperature as control parameters on timescales ranging from 10^(-12) to 10^3 s. The introduction of a time-domain axis in the phase diagram enables us to follow the evolution of metastable emergent states created by different phase transition mechanisms on different timescales, thus enabling comparison with theoretical predictions of the phase diagram and opening the way to understanding of the complex ordering processes in metastable materials.

cond-mat.str-el