arXiv subjects

Thibault Chervy

Publications and source records attributed to Thibault Chervy.

15 recordsLinked to original sources

arXiv2026

Photon correlation microscopy of quantum matter

Light and matter share fundamental statistical properties, yet the experimental probes of quantum optics and many-body physics have largely evolved along separate trajectories. While many-body physics explores emergent collective phenomena, quantum optics has refined the measurement of correlations between individual photons. Here, we introduce photon correlation microscopy (PCM) - which bridges the two domains by leveraging correlations of emitted light to probe the correlations in quantum matter at mesoscopic scales. We demonstrate this approach using a one-dimensional (1D) ensemble of dipolar excitons confined at a lateral monolayer MoSe$_2$-WSe$_2$ heterojunction. We use gate-defined potentials to confine the 1D excitons to a mesoscopic lengthscale to enhance the visibility of matter correlations in the emitted photon field. Power-dependent spectroscopy reveals a transition from a compressible to an incompressible phase, signaled by the simultaneous saturation of the emission intensity and energy blueshift, which is supported by numerical simulations. Through this crossover, photon correlation measurements show a striking evolution from bunching at low densities to antibunching at high densities. This constitutes a many-body blockade of photon emission emerging directly from a number-stabilized state, driven by collective dipolar repulsion. Our results establish PCM as a powerful probe of many-body physics through the lens of quantum optics, extensible to a broad class of correlated electronic phases, while pointing toward a route to generating non-classical light through many-body correlations.

cond-mat.mes-hall↗

arXiv2026

Simulation of Hopfield-like Hamiltonians using time-multiplexed photonic networks

We propose a time-multiplexed photonic network architecture based on coupled ring resonators, capable of accurately emulating specific Hamiltonian dynamics. We show that, in the Suzuki-Trotter limit, the resulting stroboscopic evolution reproduces the characteristic dynamics of the bosonized Hopfield model. Furthermore, by incorporating a nonlinear element within the main resonator loop, we outline a scalable route toward optical simulation of both mean-field and quantum nonlinear dynamics associated with the Tavis-Cummings model. Our results establish time-multiplexed resonator networks as a versatile photonic framework for simulating interacting light-matter Hamiltonians and collective many-body phenomena.

physics.optics↗

arXiv2025

Ultrafast optical gating in a nonlinear lithium niobate microcavity

Recent advances in optical simulation and computational techniques have renewed interest in high-finesse optical cavities for applications such as enhancing light-matter interactions, engineering complex photonic band structures, and storing quantum information. However, the extended interaction times enabled by these cavities often come at the cost of slow optical read-out protocols and limited control over system transients. To address this challenge, we demonstrate an ultrafast intra-cavity optical gating scheme in a high-finesse, second-order nonlinear microcavity incorporating a thin-film of lithium niobate. A femtosecond optical gate pulse -- tuned to the transparency region of the cavity's dielectric mirrors -- achieves instantaneous up-conversion of the intra-cavity field via sum-frequency generation. The resulting upconverted signal exits the cavity as a short pulse, providing space- and time-resolved, on-demand access to the intra-cavity state. We validate this approach by tracking the dynamics of multiple resonant modes excited in a plano-concave distributed Bragg reflector microcavity, showing close agreement with analytical models. Additionally, we demonstrate that stimulated intra-cavity difference-frequency generation can efficiently instantiate cavity modes on femtosecond timescales. This gating scheme is fully compatible with low-temperature microcavity experiments, paving the way for advanced quantum state storage, retrieval, and real-time control of light-matter interactions.

physics.optics↗

arXiv2025

Dipolar excitonic quantum wires at atomically sharp lateral interfaces

One-dimensional (1D) quantum systems are a cornerstone of many-body physics. However, their realization in solids has traditionally relied on top-down methods, which are limited by structural disorder and coarse confinement. Here, we demonstrate a fundamentally distinct route: the emergence of 1D quantum matter at the atomically sharp interface between monolayer semiconductors. Using lateral $MoSe_2-WSe_2$ heterostructures, we identify interfacial excitonic quasiparticles that are bound to the crystal junction. Photoluminescence spectroscopy resolves these excitons into a ladder of discrete states, establishing nanoscopic 1D confinement at length scales of 3 nm. These excitons possess exceptional large permanent in-plane electric dipole moments exceeding e x 2 nm, and exhibit micron-scale, highly anisotropic diffusion confined to the interface. Crucially, the lateral geometry enables dynamic, in-situ reconfiguration of the exciton's internal structure. By introducing electrostatic doping, we demonstrate a collapse of the dipole moment and a 20-fold reduction in radiative lifetime. This structural tunability establishes lateral interfaces as a uniquely powerful platform for the 'bottom-up' engineering of 1D quantum matter. By enabling the dynamic tuning of wavefunctions within a single atomic monolayer, this work opens a scalable route toward 1D excitonic circuits and strongly correlated 1D bosonic phases.

cond-mat.mes-hall↗

arXiv2025

Roadmap for Photonics with 2D Materials

Triggered by the development of exfoliation and the identification of a wide range of extraordinary physical properties in self-standing films consisting of one or few atomic layers, two-dimensional (2D) materials such as graphene, transition metal dichalcogenides (TMDs), and other van der Waals (vdW) crystals currently constitute a wide research field protruding in multiple directions in combination with layer stacking and twisting, nanofabrication, surface-science methods, and integration into nanostructured environments. Photonics encompasses a multidisciplinary collection of those directions, where 2D materials contribute with polaritons of unique characteristics such as strong spatial confinement, large optical-field enhancement, long lifetimes, high sensitivity to external stimuli (e.g., electric and magnetic fields, heating, and strain), a broad spectral range from the far infrared to the ultraviolet, and hybridization with spin and momentum textures of electronic band structures. The explosion of photonics with 2D materials as a vibrant research area is producing breakthroughs, including the discovery and design of new materials and metasurfaces with unprecedented properties as well as applications in integrated photonics, light emission, optical sensing, and exciting prospects for applications in quantum information, and nanoscale thermal transport. This Roadmap summarizes the state of the art in the field, identifies challenges and opportunities, and discusses future goals and how to meet them through a wide collection of topical sections prepared by leading practitioners.

cond-mat.mtrl-sci↗

arXiv2023

Quantum control of exciton wavefunctions in 2D semiconductors

Excitons -- bound electron-hole pairs -- play a central role in light-matter interaction phenomena, and are crucial for wide-ranging applications from light harvesting and generation to quantum information processing. A long-standing challenge in solid-state optics has been to achieve precise and scalable control over the quantum mechanical state of excitons in semiconductor heterostructures. Here, we demonstrate a technique for creating tailored and tunable potential landscapes for optically active excitons in 2D semiconductors that enables in-situ wavefunction shaping at the nanoscopic lengthscale. Using nanostructured gate electrodes, we create localized electrostatic traps for excitons in diverse geometries such as quantum dots and rings, and arrays thereof. We show independent spectral tuning of multiple spatially separated quantum dots, which allows us to bring them to degeneracy despite material disorder. Owing to the strong light-matter coupling of excitons in 2D semiconductors, we observe unambiguous signatures of confined exciton wavefunctions in optical reflection and photoluminescence measurements. Our work introduces a new approach to engineering exciton dynamics and interactions at the nanometer scale, with implications for novel optoelectronic devices, topological photonics, and many-body quantum nonlinear optics.

cond-mat.mes-hall↗

arXiv2022

Tunable quantum confinement of neutral excitons using electric fields and exciton-charge interactions

Quantum confinement is the discretization of energy when motion of particles is restricted to length scales smaller than their de Broglie wavelength. The experimental realization of this effect has had wide ranging impact in diverse fields of physics and facilitated the development of new technologies. In semiconductor physics, quantum confinement of optically excited quasiparticles, such as excitons or trions, is typically achieved by modulation of material properties - an approach crucially limited by the lack of insitu tunability and scalability of confining potentials. Achieving fully tunable quantum confinement of optical excitations has therefore been an outstanding goal in quantum photonics. Here, we demonstrate electrically controlled quantum confinement of neutral excitons in a gate-defined monolayer p-i-n diode. A combination of dc Stark shift induced by large in-plane fields and a previously unknown confining mechanism based on repulsive interaction between excitons and free charges ensures tight exciton confinement in the narrow neutral region. Quantization of exciton motion manifests in multiple discrete, spectrally narrow, voltage-dependent optical resonances that emerge below the free exciton resonance. Our measurements reveal several unique physical features of these quantum confined excitons, including an in-plane dipolar character, one-dimensional center-of-mass confinement, and strikingly enhanced exciton size in the presence of magnetic fields. Our method provides an experimental route towards creating scalable arrays of identical single photon sources, which will constitute building blocks of strongly correlated photonic systems.

cond-mat.mes-hall↗

arXiv2021

Layered Metals as Polarized Transparent Conductors

The quest to improve transparent conductors balances two key goals: increasing electrical conductivity and increasing optical transparency. To improve both simultaneously is hindered by the physical limitation that good metals with high electrical conductivity have large carrier densities that push the plasma edge into the ultra-violet range. Transparent conductors are compromises between electrical conductivity, requiring mobile electrons, and optical transparency based on immobile charges to avoid screening of visible light. Technological solutions reflect this trade-off, achieving the desired transparencies by reducing the conductor thickness or carrier density at the expense of a lower conductance. Here we demonstrate that highly anisotropic crystalline conductors offer an alternative solution, avoiding this compromise by separating the directions of conduction and transmission. Materials with a quasi-two-dimensional electronic structure have a plasma edge well below the range of visible light while maintaining excellent in-plane conductivity. We demonstrate that slabs of the layered oxides Sr$_2$RuO$_4$ and Tl$_2$Ba$_2$CuO$_{6+δ}$ are optically transparent even at macroscopic thicknesses >2$μ$m for c-axis polarized light. Underlying this observation is the fabrication of out-of-plane slabs by focused ion beam milling. This work provides a glimpse into future technologies, such as highly polarized and addressable optical screens, that advancements in a-axis thin film growth will enable.

cond-mat.mtrl-sci↗

arXiv2021

Freeform nanostructuring of hexagonal boron nitride

Hexagonal boron nitride (hBN)-long-known as a thermally stable ceramic-is now available as atomically smooth, single-crystalline flakes, revolutionizing its use in optoelectronics. For nanophotonics, these flakes offer strong nonlinearities, hyperbolic dispersion, and single-photon emission, providing unique properties for optical and quantum-optical applications. For nanoelectronics, their pristine surfaces, chemical stability, and wide bandgap have made them the key substrate, encapsulant, and gate dielectric for two-dimensional electronic devices. However, while exploring these advantages, researchers have been restricted to flat flakes or those patterned with basic slits and holes, severely limiting advanced architectures. If freely varying flake profiles were possible, the hBN structure would present a powerful design parameter to further manipulate the flow of photons, electrons, and excitons in next-generation devices. Here, we demonstrate freeform nanostructuring of hBN by combining thermal scanning-probe lithography and reactive-ion etching to shape flakes with surprising fidelity. We leverage sub-nanometer height control and high spatial resolution to produce previously unattainable flake structures for a broad range of optoelectronic applications. For photonics, we fabricate microelements and show the straightforward transfer and integration of such elements by placing a spherical hBN microlens between two planar mirrors to obtain a stable, high-quality optical microcavity. We then decrease the patterning length scale to introduce Fourier surfaces for electrons, creating sophisticated, high-resolution landscapes in hBN, offering new possibilities for strain and band-structure engineering. These capabilities can advance the discovery and exploitation of emerging phenomena in hyperbolic metamaterials, polaritonics, twistronics, quantum materials, and 2D optoelectronic devices.

physics.optics↗

arXiv2020

Large optical nonlinearity enhancement under electronic strong coupling

Nonlinear optical responses provide a powerful way to understand the microscopic interactions between laser fields and matter. They are critical for plenty of applications, such as in lasers, integrated photonic circuits, biosensing and medical tools. However, most materials exhibit weak optical nonlinearities or long response times when they interact with intense optical fields. Here, we strongly couple the exciton of organic molecules to an optical mode of a Fabry-Perot cavity, and achieve an enhancement of the nonlinear complex refractive index by two orders of magnitude compared with that of the uncoupled condition. Moreover, the coupled system shows an ultrafast response of ~120 fs that we extract from optical cross-correlation measurements. The ultrafast and large enhancement of the nonlinar coefficients in this work paves the way for exploring strong coupling effects on various third-order nonlinear optical phenomena and for technological applications.

physics.optics↗

arXiv2020

Accelerating Polaritons with External Electric and Magnetic Fields

It is widely assumed that photons cannot be manipulated using electric or magnetic fields. Even though hybridization of photons with electronic polarization to form exciton-polaritons has paved the way to a number of ground-breaking experiments in semiconductor microcavities, the neutral bosonic nature of these quasiparticles has severely limited their response to external gauge fields. Here, we demonstrate polariton acceleration by external electric and magnetic fields in the presence of nonperturbative coupling between polaritons and itinerant electrons, leading to formation of new quasiparticles termed polaron-polaritons. We identify the generation of electron density gradients by the applied fields to be primarily responsible for inducing a gradient in polariton energy, which in turn leads to acceleration along a direction determined by the applied fields. Remarkably, we also observe that different polarization components of the polaritons can be accelerated in opposite directions when the electrons are in $ν= 1$ integer quantum Hall state.

cond-mat.mes-hall↗

arXiv2019

Exploring Superconductivity under Strong Coupling with the Vacuum Electromagnetic Field

Light-matter interactions have generated considerable interest as a means to manipulate material properties. Light-induced superconductivity has been demonstrated using pulsed lasers. An attractive alternative possibility is to exploit strong light-matter interactions arising by coupling phonons to the vacuum electromagnetic field of a cavity mode as has been suggested and theoretically studied. Here we explore this possibility for two very different superconductors, namely YBCO (YBa$_2$Cu$_3$O$_{6+x}$) and Rb$_3$C$_{60}$, coupled to surface plasmon polaritons, using a novel cooperative effect based on the presence of a strongly coupled vibrational environment allowing efficient dressing of the otherwise weakly coupled phonon bands of these compounds. By placing the superconductor-surface plasmon system in a SQUID magnetometer, we find that the superconducting transition temperatures ($T_{c}$) for both compounds are modified in the absence of any external laser field. For YBCO, $T_{c}$ decreases from 92 K to 86 K while for Rb$_3$C$_{60}$, it increases from 30 K to 45 K at normal pressures. In the latter case, a simple theoretical framework is provided to understand these results based on an enhancement of the electron-phonon coupling. This proof-of-principle study opens a new tool box to not only modify superconducting materials but also to understand the mechanistic details of different superconductors.

cond-mat.supr-con↗

arXiv2018

Room Temperature Valley Polarization and Coherence in Transition Metal Dichalcogenide-Graphene van der Waals Heterostructures

Van der Waals heterostructures made of graphene and transition metal dichalcogenides (TMD) are an emerging platform for opto-electronic, -spintronic and -valleytronic devices that could benefit from (i) strong light-matter interactions and spin-valley locking in TMDs and (ii) exceptional electron and spin transport in graphene. The operation of such devices requires significant valley polarization and valley coherence, ideally up to room temperature. Here, using a comprehensive Mueller polarimetry analysis, we report \textit{artifact-free} room temperature degrees of valley polarization up to $40~\%$ and, remarkably, of valley coherence up to $20~\%$ in monolayer tungsten disulfide (WS$_2$)/graphene heterostructures. Valley contrasts have been particularly elusive in molybdenum diselenide (MoSe$_2$), even at cryogenic temperatures. Upon interfacing monolayer MoSe$_2$ with graphene, the room temperature degrees of valley polarization and coherence are as high as $14~\%$ and $20~\%$, respectively. Our results are discussed in light of recent reports of highly efficient interlayer coupling and exciton transfer in TMD/graphene heterostructures and hold promise for room temperature chiral light-matter interactions and coherent opto-valleytronic devices.

cond-mat.mes-hall↗

arXiv2017

Spin-momentum locked polariton transport in the chiral strong coupling regime

We demonstrate room temperature chiral strong coupling of valley excitons in a transition metal dichalcogenide monolayer with spin-momentum locked surface plasmons. In this regime, we measure spin-selective excitation of directional flows of polaritons. Operating under strong light-matter coupling, our platform yields robust intervalley contrasts and coherences, enabling us to generate coherent superpositions of chiral polaritons propagating in opposite directions. Our results reveal the rich and easy to implement possibilities offered by our system in the context of chiral optical networks.

cond-mat.mtrl-sci↗

arXiv2016

Multiple Rabi Splittings under Ultra-Strong Vibrational Coupling

From the high vibrational dipolar strength offered by molecular liquids, we demonstrate that a molecular vibration can be ultra-strongly coupled to multiple IR cavity modes, with Rabi splittings reaching $24\%$ of the vibration frequencies. As a proof of the ultra-strong coupling regime, our experimental data unambiguously reveal the contributions to the polaritonic dynamics coming from the anti-resonant terms in the interaction energy and from the dipolar self-energy of the molecular vibrations themselves. In particular, we measure the opening of a genuine vibrational polaritonic bandgap of ca. $60$ meV. We also demonstrate that the multimode splitting effect defines a whole vibrational ladder of heavy polaritonic states perfectly resolved. These findings reveal the broad possibilities in the vibrational ultra-strong coupling regime which impact both the optical and the molecular properties of such coupled systems, in particular in the context of mode-selective chemistry.

quant-ph↗