arXiv subjects

Fabrizio Carbone

Publications and source records attributed to Fabrizio Carbone.

At least 37 records · Page 2Linked to original sources

arXiv2022

Nuclear Excitation by Muon Capture

Efficient excitation of nuclei via exchange of a real or virtual photon has a fundamental importance for nuclear science and technology development. Here, we present a new mechanism of nuclear excitation based on the capture of a free muon into the atomic orbits (NE$μ$C). The cross section of such a new process is evaluated using the Feshbach projection operator formalism and compared to other known excitation phenomena, i.e. photo-excitation and nuclear excitation by electron capture (NEEC), showing up to ten orders of magnitude increase in cross section. NE$μ$C is particularly interesting for MeV excitations that become accessible thanks to the stronger binding of muons to the nucleus. The binding energies of muonic atoms have been calculated introducing a state of the art modification to the Flexible Atomic Code (FAC). An analysis of an experimental scenarios in the context of modern muon production facilities shows that the effect can be detectable for selected isotopes. The total probability of NE$μ$C is predicted to be $ P \approx 10^{-6}$ per incident muon in a beam-based scenario. Given the high transition energy provided by muons, NE$μ$C can have important consequences for isomer feeding and particle-induced fission.

nucl-th↗

arXiv2022

Coherent Smith-Purcell $γ$-Ray Emission

We investigate the Smith-Purcell emission produced by electron- or ion-beam-driven coherent excitation of nuclei arranged in periodic crystal lattices. The excitation and subsequent radiative decay of the nuclei can leave the target in the initial ground state after $γ$-ray emission, thus generating a coherent superposition of the far-field photon amplitude emanating from different nuclei that results in sharp angular patterns at spectrally narrow nuclear transition energies. We focus on Fe-57 as an example of two-level nuclear lossy system giving rise to Smith-Purcell emission at 14.4\,keV with a characteristic delay of 1.2\,ns relative to the excitation time. These properties enable a clean separation from faster and spectrally broader emission mechanisms, such as bremsstrahlung. Besides its fundamental interest, our study holds potential for the design of high-energy, narrow-band, highly-directive photon sources, as well as a means to store energy in the form of nuclear excitations.

quant-ph↗

arXiv2021

Dynamical control of nuclear isomer depletion via electron vortex beams

Long-lived excited states of atomic nuclei can act as energy traps. These states, known as nuclear isomers, can store a large amount of energy over long periods of time, with a very high energy-to-mass ratio. Under natural conditions, the trapped energy is only slowly released, limited by the long isomer lifetimes. Dynamical external control of nuclear state population has proven so far very challenging, despite ground-breaking incentives for a clean and efficient energy storage solution. Here, we describe a protocol to achieve the external control of the isomeric nuclear decay by using electrons whose wavefunction has been especially designed and reshaped on demand. Recombination of these electrons into the atomic shell around the isomer can lead to the controlled release of the stored nuclear energy. On the example of $^{93m}$Mo, we show that the use of tailored electron vortex beams increases the depletion by four orders of magnitude compared to the spontaneous nuclear decay of the isomer. Furthermore, specific orbitals can sustain an enhancement of the recombination cross section for vortex electron beams by as much as six orders of magnitude, providing a handle for manipulating the capture mechanism. These findings open new prospects for controlling the interplay between atomic and nuclear degrees of freedom, with potential energy-related and high-energy radiation sources applications.

physics.atom-ph↗

arXiv2020

Ultrafast Momentum-Resolved Probing of Plasmon Thermal Dynamics with Free Electrons

Current advances in ultrafast electron microscopy make it possible to combine optical pumping of a nanostructure and electron beam probing with subångstrom and femtosecond spatiotemporal resolution. We present a theory predicting that this technique can reveal a rich out-of-equilibrium dynamics of plasmon excitations in graphene and graphite samples. In a disruptive departure from the traditional probing of nanoscale excitations based on the identification of spectral features in the transmitted electrons, we show that measurement of angle-resolved, energy-integrated inelastic electron scattering can trace the temporal evolution of plasmons in these structures and provide momentum-resolved mode identification, thus avoiding the need for highly-monochromatic electron beams and the use of electron spectrometers. This previously unexplored approach to study the ultrafast dynamics of optical excitations can be of interest to understand and manipulate polaritons in 2D semiconductors and other materials exhibiting a strong thermo-optical response.

cond-mat.mtrl-sci↗

arXiv2020

Nanoscale-femtosecond dielectric response of Mott insulators captured by two-colour near-field ultrafast electron microscopy

Characterizing and controlling the out-of-equilibrium state of nanostructured Mott insulators hold great promises for emerging quantum technologies while providing an exciting playground for investigating fundamental physics of strongly-correlated systems. Here, we use two-colour near-field ultrafast electron microscopy to photo-induce the insulator-to-metal transition in a single VO2 nanowire and probe the ensuing electronic dynamics with combined nanometer-femtosecond resolution. We take advantage of a femtosecond temporal gating of the electron pulse mediated by an infrared laser pulse, and exploit the sensitivity of inelastic electron-light scattering to changes in the material dielectric function. By spatially mapping the near-field dynamics of an individual nanowire of VO2, we observe that ultrafast photo-doping drives the system into a metallic state on a time scale of about 150 fs without yet perturbing the crystalline lattice. Due to the high versatility and sensitivity of the electron probe, our method would allow capturing the electronic dynamics of a wide range of nanoscale materials with ultimate spatio-temporal resolution.

physics.app-ph↗

arXiv2020

Electron-Phonon-Driven Three-Dimensional Metallicity in an Insulating Cuprate

The role of the crystal lattice for the electronic properties of cuprates and other high-temperature superconductors remains controversial despite decades of theoretical and experimental efforts. While the paradigm of strong electronic correlations suggests a purely electronic mechanism behind the insulator-to-metal transition, recently the mutual enhancement of the electron-electron and the electron-phonon interaction and its relevance to the formation of the ordered phases have also been emphasized. Here, we combine polarization-resolved ultrafast optical spectroscopy and state-of-the-art dynamical mean-field theory to show the importance of the crystal lattice in the breakdown of the correlated insulating state in an archetypal undoped cuprate. We identify signatures of electron-phonon coupling to specific fully-symmetric optical modes during the build-up of a three-dimensional metallic state that follows charge photodoping. Calculations for coherently displaced crystal structures along the relevant phonon coordinates indicate that the insulating state is remarkably unstable toward metallization despite the seemingly large charge-transfer energy scale. This hitherto unobserved insulator-to-metal transition mediated by fully-symmetric lattice modes can find extensive application in a plethora of correlated solids.

cond-mat.str-el↗

arXiv2019

Ultrafast electron energy-loss spectroscopy in transmission electron microscopy

In the quest for dynamic multimodal probing of a material's structure and functionality, it is critical to be able to quantify the chemical state on the atomic and nanoscale using element specific electronic and structurally sensitive tools such as electron energy loss spectroscopy (EELS). Ultrafast EELF, with combined energy, time, and spatial resolution in a transmission electron microscope, has recently enabled transformative studies of photo excited nanostructure evolution and mapping of evanescent electromagnetic fields. This article aims to describe the state of the art experimental techniques in this emerging field and its major uses and future applications.

physics.app-ph↗

arXiv2019

Stacking transition in rhombohedral graphite

Few layer graphene (FLG) has been recently intensively investigated for its variable electronic properties defined by a local atomic arrangement. While the most natural layers arrangement in FLG is ABA (Bernal) stacking, a metastable ABC (rhombohedral) stacking characterized by a relatively high energy barrier can also occur. When both stacking occur in the same FLG device this results in in-plane heterostructure with a domain wall (DW). We show that ABC stacking in FLG can be controllably and locally turned into ABA stacking by two following approaches. In the first approach, Joule heating was introduced and the transition was characterized by 2D-peak Raman spectra at a submicron spatial resolution. The observed transition was initiated at a small region and then the DW controllably shifted until the entire device became ABA stacked. In the second approach, the transition was achieved by illuminating the ABC region with a train of laser pulses of 790 nm wavelength, while the transition was visualized by transmission electron microscopy in both diffraction and dark field modes. Also, with this approach, a DW was visualized in the dark-field imaging mode, at a nanoscale spatial resolution.

cond-mat.mes-hall↗

arXiv2018

Tuning of a skyrmion cluster in magnetoelectric Cu$_2$OSeO$_3$ by electric field

Chiral magnetic textures with non-trivial topology are known as skyrmions, and due to their unique properties they are promising in novel magnetic storage applications. While the electric manipulation of either isolated skyrmions or a whole skyrmion lattice have been intensively reported, the electric effects on skyrmion clusters remain scarce. In magnetoelectric compound Cu$_2$OSeO$_3$, a skyrmion cluster can be created near the helical-skyrmion phase boundary. Here, we report the in situ electric field writing/erasing of skyrmions in such a skyrmion cluster. Our real space/time image data obtained by Lorentz transmission electron microscopy and the quantitative analysis evidence the linear increase of the number of skyrmions in the cluster upon the application of a creating electric field. The energy needed to create a single skyrmion is estimated to be $\mathcal{E}=4.7 \times 10^{-24}$ J.

cond-mat.str-el↗

arXiv2018

Local photo-mechanical stiffness revealed in gold nanoparticles supracrystals by ultrafast small-angle electron diffraction

We demonstrate that highly-ordered two-dimensional crystals of ligand-capped gold nanoparticles display a local photo-mechanical stiffness as high as that of solids such as graphite. In out-of equilibrium electron diffraction experiments, a strong temperature jump is induced in a thin film with a femtosecond laser pulse. The initial electronic excitation transfers energy to the underlying structural degrees of freedom, with a rate generally proportional to the stiffness of the material. With femtosecond small-angle electron diffraction, we observe the temporal evolution of the diffraction feature associated to the nearest-neighbor nanoparticle distance. The Debye-Waller decay for the octanethiol-capped nanoparticles supracrystal, in particular, is found to be unexpectedly fast, almost as fast as the stiffest solid known and observed by the same technique, i.e. graphite. Our observations unravel that local stiffness in a dense supramolecular assembly can be created by Van der Waals interactions up to a level comparable to crystalline systems characterized by covalent bonding.

cond-mat.mes-hall↗

arXiv2018

Melting a skyrmion lattice topologically: through the hexatic phase to a skyrmion liquid

Skyrmions are twirling magnetic textures whose non-trivial topology leads to particle-like properties promising for information technology applications. Perhaps the most important aspect of interacting particles is their ability to form thermodynamically distinct phases from gases and liquids to crystalline solids. Dilute gases of skyrmions have been realized in artificial multilayers, and solid crystalline skyrmion lattices have been observed in bulk skyrmion hosting materials. Yet, to date melting of the skyrmion lattice into a skyrmion liquid has not been reported experimentally. Through direct imaging with cryo-Lorentz transmission electron microscopy, we demonstrate that the skyrmion lattice in the material Cu$_2$OSeO$_3$ can be dynamically melted. Remarkably, we discover this melting process to be a topological defects mediated two-step transition via a theoretically hypothesized hexatic phase to the liquid phase. The existence of hexatic and liquid phases instead of a simple fading of the local magnetic moments upon thermal excitations implies that even in bulk materials skyrmions possess considerable particle nature, which is a pre-requisite for application schemes.

cond-mat.str-el↗

arXiv2018

Lattice-Mediated Magnetic Order Melting in TbMnO3

Recent ultrafast magnetic-sensitive measurements [Phys. Rev. B 92, 184429 (2015) and Phys. Rev. B 96, 184414 (2017)] have revealed a delayed melting of the long-range cycloid spin-order in TbMnO$_3$ following photoexcitation across the fundamental Mott-Hubbard gap. The microscopic mechanism behind this slow transfer of energy from the photoexcited carriers to the spin degrees of freedom is still elusive and not understood. Here, we address this problem by combining spectroscopic ellipsometry, ultrafast broadband optical spectroscopy and ab initio calculations. Upon photoexcitation, we observe the emergence of a complex collective response, which is due to high-energy coherent optical phonons coupled to the out-of-equilibrium charge density. This response precedes the magnetic order melting and is interpreted as the fingerprint of the formation of anti-Jahn Teller polarons. We propose that the charge localization in a long-lived self-trapped state hinders the emission of magnons and other spin-flip mechanisms, causing the energy transfer from the charge to the spin system to be mediated by the reorganization of the lattice. Furthermore, we provide evidence for the coherent excitation of a phonon mode associated with the ferroelectric phase transition.

cond-mat.str-el↗

arXiv2017

In situ Electric Field Skyrmion Creation in Magnetoelectric Cu$_2$OSeO$_3$

Magnetic skyrmions are localized nanometric spin textures with quantized winding numbers as the topological invariant. Rapidly increasing attention has been paid to the investigations of skyrmions since their experimental discovery in 2009, due both to the fundamental properties and the promising potential in spintronics based applications. However, controlled creation of skyrmions remains a pivotal challenge towards technological applications. Here, we report that skyrmions can be created locally by electric field in the magnetoelectric helimagnet Cu$\mathsf{_2}$OSeO$\mathsf{_3}$. Using Lorentz transmission electron microscopy, we successfully write skyrmions in situ from a helical spin background. Our discovery is highly coveted since it implies that skyrmionics can be integrated into contemporary field effect transistor based electronic technology, where very low energy dissipation can be achieved, and hence realizes a large step forward to its practical applications.

cond-mat.str-el↗

arXiv2017

Magnetic skyrmions and skyrmion clusters in the helical phase of Cu$_2$OSeO$_3$

Skyrmions are nanometric spin whirls that can be stabilized in magnets lacking inversion symmetry. The properties of isolated skyrmions embedded in a ferromagnetic background have been intensively studied. We show that single skyrmions and clusters of skyrmions can also form in the helical phase and investigate theoretically their energetics and dynamics. The helical background provides natural one-dimensional channels along which a skyrmion can move rapidly. In contrast to skyrmions in ferromagnets, the skymion-skyrmion interaction has a strong attractive component and thus skyrmions tend to form clusters with characteristic shapes. These clusters are directly observed in transmission electron microscopy measurements in thin films of Cu$_2$OSeO$_3$. Topological quantization, high mobility and the confinement of skyrmions in channels provided by the helical background may be useful for future spintronics devices.

cond-mat.str-el↗

arXiv2017

Coherent generation of symmetry-forbidden phonons by light-induced electron-phonon interactions in magnetite

Symmetry breaking across phase transitions often causes changes in selection rules and emergence of optical modes which can be detected via spectroscopic techniques or generated coherently in pump-probe experiments. In second-order or weakly first-order transitions, fluctuations of the order parameter are present above the ordering temperature, giving rise to intriguing precursor phenomena, such as critical opalescence. Here, we demonstrate that in magnetite (Fe$_3$O$_4$) light excitation couples to the critical fluctuations of the charge order and coherently generates structural modes of the ordered phase above the critical temperature of the Verwey transition. Our findings are obtained by detecting coherent oscillations of the optical constants through ultrafast broadband spectroscopy and analyzing their dependence on temperature. To unveil the coupling between the structural modes and the electronic excitations, at the origin of the Verwey transition, we combine our results from pump-probe experiments with spontaneous Raman scattering data and theoretical calculations of both the phonon dispersion curves and the optical constants. Our methodology represents an effective tool to study the real-time dynamics of critical fluctuations across phase transitions.

cond-mat.mtrl-sci↗

arXiv2017

Real-time Observation of Phonon-Mediated $σ$-$π$ Interband Scattering in MgB2

In systems having an anisotropic electronic structure, such as the layered materials graphite, graphene and cuprates, impulsive light excitation can coherently stimulate specific bosonic modes, with exotic consequences for the emergent electronic properties. Here we show that the population of E$_{2g}$ phonons in the multiband superconductor MgB$_2$ can be selectively enhanced by femtosecond laser pulses, leading to a transient control of the number of carriers in the σ-electronic subsystem. The nonequilibrium evolution of the material optical constants is followed in the spectral region sensitive to both the a- and c-axis plasma frequencies and modeled theoretically, revealing the details of the $σ$-$π$ interband scattering mechanism in MgB$_2$.

cond-mat.supr-con↗

arXiv2016

Clocking the Onset of Bilayer Coherence in a High-$\mathrm{T_C}$ Cuprate

In cuprates, a precursor state of superconductivity is speculated to exist above the critical temperature $\mathrm{T_C}$. Here we show via a combination of far-infrared ellipsometry and ultrafast broadband optical spectroscopy that signatures of such a state can be obtained via three independent observables in an underdoped sample of NdBa$_2$Cu$_3$O$_{6+δ}$. The pseudogap correlations were disentangled from the response of laser-broken pairs by clocking their characteristic time-scales. The onset of a superconducting precursor state was found at a temperature $\mathrm{T_{ONS}}$ $>$ $\mathrm{T_C}$, consistent with the temperature scale identified via static optical spectroscopy. Furthermore, the temperature evolution of the coherent vibration of the Ba ion, strongly renormalized by the onset of superconductivity, revealed a pronounced anomaly at the same temperature $\mathrm{T_{ONS}}$. The microscopic nature of such a precursor state is discussed in terms of pre-formed pairs and enhanced bilayer coherence.

cond-mat.supr-con↗

arXiv2016

Probing the coupling between a doublon excitation and the charge-density wave in TaS2 by ultrafast optical spectroscopy

Recently, the switching between the different charge-ordered phases of 1T-TaS2 has been probed by ultrafast techniques, revealing unexpected phenomena such as "hidden" metastable states and peculiar photoexcited charge patterns. Here, we apply broadband pump-probe spectroscopy with varying excitation energy to study the ultrafast optical properties of 1T-TaS2 in the visible regime. By scanning the excitation energy in the near-IR region we unravel the coupling between different charge excitations and the low-lying charge-density wave state. We find that the amplitude mode of the charge-density wave exhibits strong coupling to a long-lived doublon state that is photoinduced in the center of the star-shaped charge-ordered Ta clusters by the near-IR optical excitation.

cond-mat.str-el↗