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P. Ruello

Publications and source records attributed to P. Ruello.

9 recordsLinked to original sources

Nonlinear phononics in Bi$_2$Te$_3$ nanoscale thin films: A theoretical approach

Density Functional Theory (DFT) calculations not only allow to predict the vibrational and optical properties of solids but also to understand and disentangle the mechanisms playing a key role in the generation of coherent optical phonons. Recent experiments performed on a Bi$_2$Te$_3$ nanofilm have shown that a THz pulse launches at least a coherent $A_{1g}^1$ phonon as the transient transmittance measured using an isotropic detection scheme displays oscillations with a frequency matching the frequency of the $A_{1g}^1$ mode measured in Raman experiments. Such an observation can be explained by invoking either a sum frequency process or cubic/quartic phonon-phonon couplings as considered for Bi$_2$Se$_3$, a parent compound of Bi$_2$Te$_3$. By resorting to group theory and calculating energy surfaces from first-principles, the main phonon-phonon couplings can be identified. Furthermore, a minimal model can be built to compute the dynamics of the Raman active modes coupled to the infrared active mode driven by the experimental THz pulse. Our model firmly establishes that cubic phonon-phonon interactions are relevant as the agreement between the computed and experimental transmittance is noteworthy.

cond-mat.mtrl-sci

Superorders and acoustic modes folding in BiFeO$_3$/LaFeO$_3$ superlattices

Superlattices are materials created by the alternating growth of two chemically different materials. The direct consequence of creating a superlattice is the folding of the Brillouin zone which gives rise to additional electronic bands and phonon modes. This has been successfully exploited to achieve new transport and optical properties in semiconductor superlattices, for example. Here, we show that multiferroic BiFeO$_3$/LaFeO$_3$ superlattices are more than just periodic chemical stacking. Using transmission electron microscopy, X-ray diffraction and first-principles calculations, we demonstrate the existence of a new order of FeO$_6$ octahedra, with a period along the growth direction about twice that of the chemical supercell, i.e. a superorder. The effect of this new structural order on the lattice dynamics is studied with ultrafast optical pump-probe experiments. While a mode at 1.2 THz is attributed solely to the chemical modulation of the superlattice, the existence of another 0.7 THz mode seems to be explained only by a double Brillouin zone folding in agreement with the structural description. Our work shows that multiferroic BiFeO$_3$/LaFeO$_3$ superlattices can be used to tune the spectrum of coherent THz phonons, and potentially that of magnons or electromagnons.

cond-mat.mtrl-sci

Anisotropy in the dielectric function of Bi$_2$Te$_3$ from first principles: From the UV-visible to the infrared range

The dielectric properties of Bi$_2$Te$_3$, a layered compound crystallizing in a rhombohedral structure, are investigated by means of first-principles calculations at the random phase approximation level. A special attention is devoted to the anisotropy in the dielectric function and to the local field effects that strongly renormalize the optical properties in the UV-visible range when the electric field is polarized along the stacking axis. Furthermore, both the Born effective charges for each atom and the zone center phonon frequencies and eigenvectors needed to describe the dielectric response in the infrared range are computed. Our theoretical near-normal incidence reflectivity spectras in both the UV-visible and infrared range are in fairly good agreement with the experimental spectras, provided that the free carriers Drude contribution arising from defects is included in the infrared response. The anisotropic plasmon frequencies entering the Drude model are computed within the rigid band approximation, suggesting that a measurement of the reflectivity in the infrared range for both polarizations might allow to infer not only the type of doping but also the level of doping.

cond-mat.mtrl-sci

Non-thermal transport of energy driven by photoexcited carriers in switchable solid states of GeTe

Phase change alloys have seen widespread use from rewritable optical discs to the present day interest in their use in emerging neuromorphic computing architectures. In spite of this enormous commercial interest, the physics of carriers in these materials is still not fully understood. Here, we describe the time and space dependence of the coupling between photoexcited carriers and the lattice in both the amorphous and crystalline states of one phase change material, GeTe. We study this using a time-resolved optical technique called picosecond acoustic method to investigate the \textit{in situ} thermally assisted amorphous to crystalline phase transformation in GeTe. Our work reveals a clear evolution of the electron-phonon coupling during the phase transformation as the spectra of photoexcited acoustic phonons in the amorphous ($a$-GeTe) and crystalline ($α$-GeTe) phases are different. In particular and surprisingly, our analysis of the photoinduced acoustic pulse duration in crystalline GeTe suggests that a part of the energy deposited during the photoexcitation process takes place over a distance that clearly exceeds that defined by the pump light skin depth. In the opposite, the lattice photoexcitation process remains localized within that skin depth in the amorphous state. We then demonstrate that this is due to supersonic diffusion of photoexcited electron-hole plasma in the crystalline state. Consequently these findings prove the existence of a non-thermal transport of energy which is much faster than lattice heat diffusion.

cond-mat.mtrl-sci

Ultrafast light-induced shear strain probed by time-resolved X-ray diffraction: the model multiferroic BiFeO$_3$ as a case study

Enabling the light-control of complex systems on ultra-short timescales gives rise to rich physics with promising applications. While crucial, the quantitative determination of both the longitudinal and shear photo-induced strains still remains challenging. Here, by scrutinizing asymmetric Bragg peaks pairs $(\pm h01)$ using picosecond time-resolved X-ray diffraction experiments in BiFeO$_3$, we simultaneously determine the longitudinal and shear strains. The relative amplitude of those strains can be explained only if both thermal and non-thermal processes contribute to the acoustic phonon photogeneration process. Importantly, we also reveal a difference of the dynamical response of the longitudinal strain with respect to the shear one due to an interplay of quasi-longitudinal and quasi-transverse acoustic modes, well reproduced by our model.

cond-mat.mtrl-sci

Ultrafast non-thermal laser excitation of gigahertz longitudinal and shear acoustic waves in spin-crossover molecular crystals [$Fe(PM-AzA)_{2}$$(NCS)_{2}$]

We report GHz longitudinal as well as shear acoustic phonons photoexcitation and photodetection using femtosecond laser pulses in a spin-crossover molecular crystal. From our experimental observation of time domain Brillouin scattering triggered by the photoexcitation of acoustic waves across the low-spin (LS) to high-spin (HS) thermal crossover, we reveal a link between molecular spin state and photoexcitation of coherent GHz acoustic phonons. In particular, we experimentally evidence an unconventional non-thermal pathway for the laser excitation of GHz phonons. We also provide experimental insight on the optical and mechanical parameters evolution across the LS/HS spin crossover temperature T$_{1/2}$.

cond-mat.mtrl-sci

Ultrafast light-induced Coherent Optical and Acoustic Phonons in few Quintuple Layers of Topological Insulators Bi2Te3

Ultrafast lattice dynamics of few quintuple layers of topological insulator (TI) Bi$_2$Te$_3$ is studied with time-resolved optical pump-probe spectroscopy. Both optical and acoustic phonons are photogenerated and detected. Here, in order to get new insights on the out-of-equilibrium electron-phonon coupling and phonons dynamics in confined TI, different nanostructures have been investigated (single or polycrystalline QLs assemblies and nano-crystallized islands). Contrary to previous literature claims, we show that even for nanostructures containing only 10 quintuple layers (QLs), the symmetric A1g(I) coherent optical phonon is efficiently photogenerated and no restriction due to the structural confinement appears. We also observe that whatever the arrangement of the nanostructures, the A1g(I) optical phonon features are similar (lifetime). We also report the observation of confined coherent acoustic phonons propagating from QLs to QLs whose spectrum is, this time, very sensitive to the atomic arrangement. In the case of the single crystalline ultrathin film, the time of flight analysis of these acoustic phonons provides direct estimate of the elastic properties of these nanostructures as well as some estimates of Van der Waals interactions between QLs.

cond-mat.mtrl-sci

Ultrafast Acousto-Plasmonics in Gold Nanoparticles Superlattice

We report the investigation of the generation and detection of GHz coherent acoustic phonons in plasmonic gold nanoparticles superlattices (NPS). The experiments have been performed from an optical femtosecond pump-probe scheme across the optical plasmon resonance of the superlattice. Our experiments allow to estimate the collective elastic response (sound velocity) of the NPS as well as an estimate of the nano-contact elastic stiffness. It appears that the light-induced coherent acoustic phonon pulse has a typical in-depth spatial extension of about 45 nm which is roughly 4 times the optical skin depth in gold. The modeling of the transient optical reflectivity indicates that the mechanism of phonon generation is achieved through ultrafast heating of the NPS assisted by light excitation of the volume plasmon. These results demonstrate how it is possible to map the photon-electron-phonon interaction in subwavelength nanostructures.

cond-mat.mtrl-sci

Coherent acoustic phonons emission in copper driven by super-diffusive hot electrons

Ultrafast laser excited hot electrons can transport energy supersonically far from the region where they are initially produced. We show that this ultrafast energy transport is responsible of the emission of coherent acoustic phonons deeply beneath the free surface of a copper metal sample. In particular we demonstrate that enough energy carried by these hot electrons over a distance as large as 220nm at room temperature in copper can be converted into coherent acoustic phonons. In order to demonstrate this effect, several configurations of time-resolved optical experiments of time of flight of coherent acoustic phonons and of hot electrons have been performed.

cond-mat.mtrl-sci