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Davide Tedeschi

Publications and source records attributed to Davide Tedeschi.

11 recordsLinked to original sources

Searching for Axions on a Higher Note: Third-Harmonic Generation from Colliding High-Intensity Laser Beams

We propose a new laboratory strategy to generate and detect axion-like particles via third-harmonic generation induced by two non-collinear, polarised high-intensity laser beams of peak intensity of the order of $10^{24}\,\mathrm{W/cm^2}$, where the third-harmonic signal is generated by the axion field. Starting from the axion-modified Maxwell equations, we analytically derive the axion-induced third-harmonic field, and show that by using state-of-the-art petawatt laser facilities, a detectable signal can be obtained over a broad range of axion masses and couplings. A key feature of the setup is that the axion-photon conversion rate can be resonantly enhanced by tuning the angle between the two beams through a mechanism that does not depend on the physical volume of the apparatus. The proposed configuration may therefore probe an unexplored region of axion parameter space and pave the way for next-generation high-power laser-based axion searches.

hep-ph

Enantio-selective inverse Faraday effect in isotropic chiral molecular mixtures

Enantiomeric excess detection in a chiral molecular mixture is paramount because very often opposite enantiomers exhibit profound functional dissimilarities that play decisive roles in biochemical applications. Existing chiral sensing methods mostly rely on large operational sample volumes, hindering compatibility with integrated sensing schemes. Here, we propose a novel chiroptical sensing technique based on the inverse Faraday effect in a photonic micro-capillary filled with nl-volume chiral drug solution. We theoretically demonstrate that, upon excitation by intense laser light, an isotropic assembly of chiral drugs produces a static magnetisation, with amplitude and direction depending on the enantiomeric excess. In turn, by measuring the chirally-sensitive static magnetic field in the vicinity of the micro-tube one can retrieve the enantiomeric excess of the chiral drug solution. Our theoretical predictions unlock new opportunities for the development of innovative nanophotonic devices suitable for efficient chiroptical sensing with nl-volume sensitivity.

physics.optics

Chirally-sensitive optical rectification by isotropic chiral media

Chiroptical sensing is central to gain fundamental insight into electronic, vibrational and rotational degrees of freedom of chiral molecules, and is a cornerstone for nanomedicine and drug discovery platforms. Current chiral sensing technologies to assess the enantiomeric imbalance of chiral pharmaceutical compounds are sensitive to ml volumes but are time-consuming and cannot be integrated on a chip, thus creating a major bottleneck for drug discovery and nanomedicine. Here, we propose a novel chiroptical sensing approach based on optical rectification in a photonic micro-cavity filled by a drug solution with nl volume. We theoretically demonstrate that, upon optical excitation by intense pulsed laser light, such a nonlinear effect produces a chirally-sensitive nV voltage burst at the electrically-gated micro-cavity boundaries, with sign depending solely on the drug enantiomeric imbalance. Our results shed light on the potential of optical rectification as a robust platform for innovative lab-on-a-chip devices enabling chiral sensing with nl sensitivity.

physics.optics

Femtosecond self-diffraction as a measure of the nonlinear response spectrum

Self diffraction is a four-wave mixing process proportional to the square modulus of third-order nonlinearity susceptibility $χ^{(3)}$, which is related to the material's electronic and thermal properties. In this study, we investigate the wavelength dependence of the self-diffracted signal generated by a femtosecond pulsed laser in a dye solution to directly evaluate the electronic third-order nonlinear susceptibility spectrum. By accounting for absorption effects and phase matching conditions, we determine the $\vertχ^{(3)}\vert$ for different concentrations. Experimental results complemented with theoretical predictions, show that in the low absorption and thin sample limits, the signal reproduce the $\vertχ^{(3)}\vert$ spectral profile. These findings demonstrate the feasibility of measuring nonlinear susceptibility spectra arising solely from the bound-electronic response across a wide spectral range and for various compounds.

physics.optics

Enhanced vibrational optical activity by near-zero index chiral effective media

The enhancement of the inherently weak optical activity of solvated molecules by superchiral fields, crucial for detecting their chirality, is a research frontier of photonics and the basis of novel chiroptical detection schemes. Here, we show that an effective medium consisting of randomly dispersed metal-based nanoparticles embedded within an optically active solvated drug (aqueous reparixin) can enhance vibrational optical rotation and circular dichroism thanks to superchirality produced by slow light in near-zero index conditions. We evaluate from first principles the effective bianisotropic response of the bulk chiral effective medium, showing that, by adjusting the nanoparticles filling fraction, vibrational optical activity is greatly enhanced by a factor $\simeq 10^2-10^3$ at the near-zero index resonance. Our results are relevant for the development of innovative devices capable of detecting the chirality of low-volume samples, with applications in quantum chemistry and nanomedicine.

physics.optics

Strain-induced dynamic control over the population of quantum emitters in two-dimensional materials

The discovery of quantum emitters (QEs) in two-dimensional materials (2D) has triggered a surge of research to assess their suitability for quantum photonics. While their microscopic origin is still the subject of intense studies, position-controlled QEs are routinely fabricated using static strain gradients, which are used to drive excitons towards localized regions of the crystal where quantum light emission takes place. However, the use of strain in a dynamic fashion to control the brightness of single-photon sources in 2D materials has not been explored so far. In this work, we address this challenge by introducing a novel hybrid semiconductorpiezoelectric device in which WSe2 monolayers are integrated onto piezoelectric pillars that provide both static and dynamic strains. The static strains are first used to induce the formation of QEs, whose emission shows photon anti-bunching. Their energy and brightness are then controlled via the application of voltages to the piezoelectric pillars. Numerical simulations combined with drift-diffusion equations show that these effects are due to a strain-induced modification of the confining-potential landscape, which in turn leads to a net redistribution of excitons among the different QEs. Our work provides a method to dynamically control the brightness of single photon sources based on 2D materials.

cond-mat.mtrl-sci

Proton-driven patterning of bulk transition metal dichalcogenides

At the few-atom-thick limit, transition metal dichalcogenides (TMDs) exhibit a host of attractive electronic optical, and structural properties. The possibility to pattern these properties has a great impact on applied and fundamental research. Here, we demonstrate spatial control over the light emission, lattice deformation, and hydrogen storage in bulk TMDs. By low-energy proton irradiation, we create uniquely favorable conditions for the production and accumulation of molecular hydrogen just one or few monolayers beneath the crystal basal plane of bulk WS2, WSe2, WTe2, MoSe2, and MoS2 samples. H2 therein produced coalesces to form bubbles, which lead to the localized swelling of one X-M-X plane prevalently. This results eventually in the creation of atomically thin domes filled with molecular hydrogen at 10 atm. The domes emit light strongly well above room temperature and can store H2 indefinitely. They can be produced with the desired density, well-ordered positions, and size tunable from the nanometer to the micrometer scale, thus providing a template for the manageable and durable mechanical and electronic structuring of two-dimensional materials.

cond-mat.mtrl-sci

Quantum Teleportation with Imperfect Quantum Dots

Efficient all-photonic quantum teleportation requires fast and deterministic sources of highly indistinguishable and entangled photons. Solid-state-based quantum emitters--notably semiconductor quantum dots--are a promising candidate for the role. However, despite the remarkable progress in nanofabrication, proof-of-concept demonstrations of quantum teleportation have highlighted that imperfections of the emitter still place a major roadblock in the way of applications. Here, rather than focusing on source optimization strategies, we deal with imperfections and study different teleportation protocols with the goal of identifying the one with maximal teleportation fidelity. Using a quantum dot with sub-par values of entanglement and photon indistinguishability, we show that the average teleportation fidelity can be raised from below the classical limit to 0.842(14). Our results, which are backed by a theoretical model that quantitatively explains the experimental findings, loosen the very stringent requirements set on the ideal entangled-photon source and highlight that imperfect quantum dots can still have a say in teleportation-based quantum communication architectures.

quant-ph

Strain-tunable Single Photon Sources in WSe2 Monolayers

The appearance of single photon sources in atomically thin semiconductors holds great promises for the development of a flexible and ultra-compact quantum technology, in which elastic strain engineering can be used to tailor their emission properties. Here, we show a compact and hybrid 2D-semiconductor-piezoelectric device that allows for controlling the energy of single photons emitted by quantum emitters localized in wrinkled WSe2 monolayers. We demonstrate that strain fields exerted by the piezoelectric device can be used to tune the energy of localized excitons in WSe2 up to 18 meV in a reversible manner, while leaving the single photon purity unaffected over a wide range. Interestingly, we find that the magnitude and in particular the sign of the energy shift as a function of stress is emitter dependent. With the help of finite element simulations we suggest a simple model that explains our experimental observations and, furthermore, discloses that the type of strain (tensile or compressive) experienced by the quantum emitters strongly depends on their localization across the wrinkles. Our findings are of strong relevance for the practical implementation of single photon devices based on two-dimensional materials as well as for understanding the effects of strain on their emission properties.

cond-mat.mes-hall

Common nonlinear features and spin-orbit coupling effects in the Zeeman splitting of novel wurtzite materials

The response of semiconductor materials to external magnetic fields is a reliable approach to probe intrinsic electronic and spin-dependent properties. In this study, we investigate the common Zeeman splitting features of novel wurtzite materials, namely InP, InAs, and GaAs. We present values for the effective g-factors of different energy bands and show that spin-orbit coupling effects, responsible for the spin splittings, also have noticeable contributions to the g-factors. Within the Landau level picture, we show that the nonlinear Zeeman splitting recently explained in magneto photoluminescence experiments for InP nanowires by Tedeschi et al. [Phys. Rev. B 99, 161204 (2019)] are also present in InAs, GaAs and even in the conventional GaN. Such nonlinear features stem from the peculiar coupling of the A and B valence bands, as a consequence of the interplay between the wurtzite crystal symmetry and the breaking of time-reversal symmetry by the external magnetic field. Moreover, we develop an analytical model to describe the experimental nonlinear Zeeman splitting and apply it to InP and GaAs data. Extrapolating our fitted results, we found that the Zeeman splitting of InP reaches a maximum value, which is a prediction that could be probed at higher magnetic fields.

cond-mat.mes-hall

Entanglement swapping with photons generated on-demand by a quantum dot

Photonic entanglement swapping, the procedure of entangling photons without any direct interaction, is a fundamental test of quantum mechanics and an essential resource to the realization of quantum networks. Probabilistic sources of non-classical light can be used for entanglement swapping, but quantum communication technologies with device-independent functionalities demand for push-button operation that, in principle, can be implemented using single quantum emitters. This, however, turned out to be an extraordinary challenge due to the stringent requirements on the efficiency and purity of generation of entangled states. Here we tackle this challenge and show that pairs of polarization-entangled photons generated on-demand by a GaAs quantum dot can be used to successfully demonstrate all-photonic entanglement swapping. Moreover, we develop a theoretical model that provides quantitative insight on the critical figures of merit for the performance of the swapping procedure. This work shows that solid-state quantum emitters are mature for quantum networking and indicates a path for scaling up.

quant-ph