Enhanced generation of non-degenerate photon-pairs in nonlinear metasurfaces

We reveal a novel regime of photon-pair generation driven by the interplay of multiple bound states in the continuum resonances in nonlinear metasurfaces. This non-degenerate photon-pair generation is derived from the hyperbolic topology of the transverse phase-matching and can enable orders-of-magnitude enhancement of the photon rate and spectral brightness, as compared to the degenerate regime. We show that the entanglement of the photon-pairs can be tuned by varying the pump polarization, which can underpin future advances and applications of ultra-compact quantum light sources

Pump-Selective Spectral Shaping of the Ultrafast Response in Plasmonic Nanostars

Plasmonic nanostructures are, to date, well-known to offer unique possibilities for the tailoring of light–matter interactions at the nanoscale. Most recently, a new route to ultrafast all-optical modulation has been disclosed by combining the resonant features of plasmonic nanostructures with the giant third-order optical nonlinearity of noble metals regulated by highly energetic (hot) carriers. In this framework, a variety of nanostructures have been designed, with special attention to shapes featuring tips, where extreme and highly sensitive field enhancements (hot spots) can be attained. Here, we report on a broadband pump–probe spectroscopy analysis of an ensemble of spiky star-shaped nanoparticles, exploring both the perturbative and nonperturbative regimes of photoexcitation. The experiments are corroborated by semiclassical numerical simulations of the ultrafast optical response of the sample. We found that the peculiar hot spots supported by the star tips allow one to easily control the spectral shape of the transient optical signal, upon tuning of the pump wavelength. Our results elucidate the ultrafast response of hot electrons in star-shaped nanostructures and contribute to the understanding of the tip-mediated enhanced nonlinearities. This work paves the way to the development of ultrafast all-optical plasmonic modulators for pump-selective spectral shaping

All-optical Reconfiguration of Ultrafast Dichroism in Gold Metasurfaces

Optical metasurfaces have come into the spotlight as a promising platform for light manipulation at the nanoscale, including ultrafast all-optical control via excitation with femtosecond laser pulses. Recently, dichroic metasurfaces have been exploited to modulate the polarization state of light with unprecedented speed. Here, we theoretically predict and experimentally demonstrate by pump-probe spectroscopy the capability to reconfigure the ultrafast dichroic signal of a gold metasurface by simply acting on the polarization of the pump pulse, which is shown to reshape the spatio-temporal distribution of the optical perturbation. The photoinduced anisotropic response, driven by out-of-equilibrium carriers and extinguished in a sub-picosecond temporal window, is readily controlled in intensity by tuning the polarization direction of the excitation up to a full sign reversal. This work proves that nonlinear metasurfaces offer the flexibility to tailor their ultrafast optical response in a fully all-optically reconfigurable platform

THz-photonics transceivers by all-dielectric phonon-polariton nonlinear nanoantennas

The THz spectrum (spanning from 0.3 to 30 THz) offers the potential of a plethora of applications, ranging from the imaging through non transparent media to wireless-over-fiber communications and THz-photonics. The latter framework would greatly benefit from the development of optical-to-THz wavelength converters. Exploiting Difference Frequency Generation in a nonlinear all dielectric nanoantenna, we propose a compact solution to this problem. By means of a near-infrared pump beam (at ?1), the information signal in the optical domain (at ?2) is converted to the THz band (at ?3=?2-?1). The approach is completely transparent with respect to the modulation format, and can be easily integrated in a metasurface platform for simultaneous frequency and spatial moulding of THz beams

Chemically-Controlled Ultrafast Photothermal Response in Plasmonic Nanostructured Assemblies

Plasmonic nanoparticles are renowned as efficient heaters due to their capability to resonantly absorb and concentrate electromagnetic radiation, trigger excitation of highly energetic (hot) carriers, and locally convert their excess energy into heat via ultrafast nonradiative relaxation processes. Furthermore, in assembly configurations (i.e., suprastructures), collective effects can even enhance the heating performance. Here, we report on the dynamics of photothermal conversion and the related nonlinear optical response from water-soluble nanoeggs consisting of a Au nanocrystal assembly trapped in a water-soluble shell of ferrite nanocrystals (also called colloidosome) of ∼250–300 nm in size. This nanoegg configuration of the plasmonic assembly enables control of the size of the gold suprastructure core by changing the Au concentration in the chemical synthesis. Different metal concentrations are analyzed by means of ultrafast pump–probe spectroscopy and semiclassical modeling of photothermal dynamics from the onset of hot-carrier photogeneration (few picosecond time scale) to the heating of the matrix ligands in the suprastructure core (hundreds of nanoseconds). Results show the possibility to design and tailor the photothermal properties of the nanoeggs by acting on the core size and indicate superior performances (both in terms of peak temperatures and thermalization speed) compared to conventional (unstructured) nanoheaters of comparable size and chemical composition

Photoinduced Temperature Gradients in Sub-wavelength Plasmonic Structures: The Thermoplasmonics of Nanocones

Plasmonic structures are renowned for their capability to efficiently convert light into heat at the nanoscale. However, despite the possibility to generate deep sub-wavelength electromagnetic hot spots, the formation of extremely localized thermal hot spots is an open challenge of research, simply because of the diffusive spread of heat along the whole metallic nanostructure. Here we tackle this challenge by exploiting single gold nanocones. We theoretically show how these structures can indeed realize extremely high temperature gradients within the metal, leading to deep sub-wavelength thermal hot spots, owing to their capability of concentrating light at the apex under resonant conditions even under continuous wave illumination. A three-dimensional Finite Element Method model is employed to study the electromagnetic field in the structure and subsequent thermoplasmonic behaviour, in terms of the three-dimensional temperature distribution. We show how the latter is affected by nanocone size, shape, and composition of the surrounding environment. Finally, we anticipate the use of photoinduced temperature gradients in nanocones for applications in optofluidics and thermoelectrics or for thermally induced nanofabrication

Transient optical symmetry breaking for ultrafast broadband dichroism in plasmonic metasurfaces

Ultrafast nanophotonics is an emerging research field aimed at the development of nanodevices capable of light modulation with unprecedented speed. A promising approach exploits the optical nonlinearity of nanostructured materials (either metallic or dielectric) to modulate their effective permittivity via interaction with intense ultrashort laser pulses. While the ultrafast temporal dynamics of such nanostructures following photoexcitation has been studied in depth, sub-ps transient spatial inhomogeneities taking place at the nanoscale have been so far almost ignored. Here we theoretically predict and experimentally demonstrate that the inhomogeneous space-time distribution of photogenerated hot carriers induces a transient symmetry breaking in a plasmonic metasurface made of highly symmetric metaatoms. The process is fully reversible, and results in a broadband transient dichroic optical response with a recovery of the initial isotropic state in less than 1 picosecond, overcoming the speed bottleneck caused by slower relaxation processes, such as electron-phonon and phonon-phonon scattering. Our results pave the way to the development of ultrafast dichroic devices, capable of Tera bit/s modulation of light polarization

Thermometric Calibration of the Ultrafast Relaxation Dynamics in Plasmonic Au Nanoparticles

The excitation of plasmonic nanoparticles by ultrashort laser pulses sets in motion a complex ultrafast relaxation process involving the gradual re-equilibration of the system's electron gas, lattice and environment. One of the major hurdles in studying these processes is the lack of direct measurements of the dynamic temperature evolution of the system subcomponents. We measured the dynamic optical response of ensembles of plasmonic Au nanoparticles following ultrashort-pulse excitation and we compared it with the corresponding static optical response as a function of the increasing temperature of the thermodynamic bath. Evaluating the two sets of data, the optical fingerprints of equilibrium or off-equilibrium responses could be clearly identified, allowing us to extract a dynamic thermometric calibration scale of the relaxation process, yielding the experimental ultrafast temperature evolution of the plasmonic particles as a function of time

Nonlinear THz Generation through Optical Rectification Enhanced by Phonon–Polaritons in Lithium Niobate Thin Films

We investigate nonlinear THz generation from lithium niobate films and crystals of different thicknesses by optical rectification of near-infrared femtosecond pulses. A comparison between numerical studies and polarization-resolved measurements of the generated THz signal reveals a 2 orders of magnitude enhancement in the nonlinear response compared to optical frequencies. We show that this enhancement is due to optical phonon modes at 4.5 and 7.45 THz and is most pronounced for films thinner than 2 μm where optical-to-THz conversion is not limited by self-absorption. These results shed new light on the employment of thin film lithium niobate platforms for the development of new integrated broadband THz emitters and detectors. This may also open the door for further control (e.g., polarization, directivity, and spectral selectivity) of the process in nanophotonic structures, such as nanowires and metasurfaces, realized in the thin film platform. We illustrate this potential by numerically investigating optical-to-THz conversion driven by localized surface phonon–polariton resonances in sub-wavelength lithium niobate rods

Ultrafast Plasmonics Beyond the Perturbative Regime: Breaking the Electronic-Optical Dynamics Correspondence

The transient optical response of plasmonic nanostructures has recently been the focus of extensive research. Accurate prediction of the ultrafast dynamics following excitation of hot electrons by ultrashort laser pulses is of major relevance in a variety of contexts from the study of light harvesting and photocatalytic processes to nonlinear nanophotonics and the all-optical modulation of light. So far, all studies have assumed the correspondence between the temporal evolution of the dynamic optical signal, retrieved by transient absorption spectroscopy, and that of the photoexcited hot electrons, described in terms of their temperature. Here, we show both theoretically and experimentally that this correspondence does not hold under a nonperturbative excitation regime. Our results indicate that the main mechanism responsible for the breaking of the correspondence between electronic and optical dynamics is universal in plasmonics, being dominated by the nonlinear smearing of the Fermi–Dirac occupation probability at high hot-electron temperatures