arXiv subjects

Thomas W. Ebbesen

Publications and source records attributed to Thomas W. Ebbesen.

17 recordsLinked to original sources

arXiv2021

Planar chirality and optical spin-orbit coupling for chiral Fabry-Perot cavities

We design, in a most simple way, Fabry-Perot cavities with longitudinal chiral modes by sandwiching between two smooth metallic silver mirrors a layer of polystyrene made planar chiral by torsional shear stress. We demonstrate that the helicity-preserving features of our cavities stem from a spin-orbit coupling mechanism seeded inside the cavities by the specific chiroptical features of planar chirality. Planar chirality gives rise to an extrinsic source of three-dimensional chirality under oblique illumination that endows the cavities with enantiomorphic signatures measured experimentally and simulated with excellent agreement. The simplicity of our scheme is particularly promising in the context of chiral cavity QED and polaritonic asymmetric chemistry.

physics.optics↗

arXiv2021

Large Enhancement of Ferro-Magnetism under Collective Strong Coupling of YBCO Nanoparticles

Light-matter strong coupling in the vacuum limit has been shown to enhance material properties over the past decade. Oxide nanoparticles are known to exhibit weak ferromagnetism due to vacancies in the lattice. Here we report the 700-fold enhancement of the ferromagnetism of YBa$_2$Cu$_3$O$_{7-x}$ nanoparticles under cooperative strong coupling at room temperature. The magnetic moment reaches 0.90 $μ_{\rm B}$/mol, and with such a high value, it competes with YBa$_2$Cu$_3$O$_{7-x}$ superconductivity at low temperature. This strong ferromagnetism at room temperature suggest that strong coupling is a new tool for the development of next generations of magnetic and spintronic nanodevices.

cond-mat.mtrl-sci↗

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

Ensemble-induced strong light-matter coupling of a single quantum emitter

We discuss a technique to strongly couple a single target quantum emitter to a cavity mode, which is enabled by virtual excitations of a nearby mesoscopic ensemble of emitters. A collective coupling of the latter to both the cavity and the target emitter induces strong photon non-linearities in addition to polariton formation, in contrast to common schemes for ensemble strong coupling. We demonstrate that strong coupling at the level of a single emitter can be engineered via coherent and dissipative dipolar interactions with the ensemble, and provide realistic parameters for a possible implementation with SiV$^{-}$ defects in diamond. Our scheme can find applications, amongst others, in quantum information processing or in the field of cavity-assisted quantum chemistry.

quant-ph↗

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↗

arXiv2019

Enhancement of the electron-phonon scattering induced by intrinsic surface plasmon-phonon polaritons

We investigate light-matter coupling in metallic crystals where plasmons coexist with phonons exhibiting large oscillator strength. We demonstrate theoretically that this coexistence can lead to strong light-matter interactions without external resonators. When the frequencies of plasmons and phonons are comparable, hybridization of these collective matter modes occurs in the crystal. We show that the coupling of these modes to photonic degrees of freedom gives rise to intrinsic surface plasmon-phonon polaritons, which offer the unique possibility to control the phonon properties by tuning the electron density and the crystal thickness. In particular, dressed phonons with reduced frequency and large wave vectors arise in the case of quasi-2D crystals, which leads to large enhancements of the electron-phonon scattering in the vibrational ultrastrong coupling regime. This suggests that photons can play a key role in determining the quantum properties of certain materials. A non-perturbative self-consistent Hamiltonian method is presented that is valid for arbitrarily large coupling strengths.

cond-mat.mes-hall↗

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

Non-Local Control of Single Surface Plasmon

Quantum entanglement is a stunning consequence of the superposition principle. This universal property of quantum systems has been intensively explored with photons, atoms, ions and electrons. Collective excitations such as surface plasmons exhibit quantum behaviors. For the first time, we report an experimental evidence of non-local control of single plasmon interferences through entanglement of a single plasmon with a single photon. We achieved photon-plasmon entanglement by converting one photon of an entangled photon pair into a surface plasmon. The plasmon is tested onto a plasmonic platform in a Mach-Zehnder interferometer. A projective measurement on the polarization of the photon allows the non-local control of the interference state of the plasmon. Entanglement between particles of various natures paves the way to the design of hybrid systems in quantum information networks.

quant-ph↗

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↗

arXiv2015

Coherent coupling of molecular resonators with a micro-cavity mode

The optical hybridization of the electronic states in strongly coupled molecule-cavity systems have revealed unique properties such as lasing, room temperature polariton condensation, and the modification of excited electronic landscapes involved in molecular isomerization. Here we show that molecular vibrational modes of the electronic ground state can also be coherently coupled with a micro-cavity mode at room temperature, given the low vibrational thermal occupation factors associated with molecular vibrations, and the collective coupling of a large ensemble of molecules immersed within the cavity mode volume. This enables the enhancement of the collective Rabi-exchange rate with respect to the single oscillator coupling strength. The possibility of inducing large shifts in the vibrational frequency of selected molecular bonds should have immediate consequences for chemistry.

quant-ph↗

arXiv2015

Mechanical separation of chiral dipoles by chiral light

We calculate optical forces and torques exerted on a chiral dipole by chiral light fields and reveal genuinely chiral forces in combining the chiral contents of both light field and dipolar matter. Here, the optical chirality is characterized in a general way through the definition of optical chirality density and chirality flow. We show in particular that both terms have mechanical effects associated respectively with reactive and dissipative components of the chiral forces. Remarkably, these chiral force components are directly related to standard observables: optical rotation for the reactive component and circular dichroism for the dissipative one. As a consequence, the resulting forces and torques are dependent on the enantiomeric form of the chiral dipole. This suggests promising strategies for using chiral light forces to mechanically separate chiral objects according to their enantiomeric form.

physics.optics↗

arXiv2015

Force and torque on an electric dipole by spinning light fields

We calculate the optical force and torque applied to an electric dipole by a spinning light field. We find that the dissipative part of the force depends on the orbital energy flow of the field only, because the latter is related to the phase gradient generalized for such a light field. As for the remaining spin energy flow, it gives rise to an optical torque. The resulting change in the optical force is detailed for different experimentally relevant configurations, and we show in particular how this change is critical when surface plasmon modes are involved.

physics.optics↗

arXiv2013

Non-markovian polariton dynamics in organic strong coupling

Strongly coupled organic systems are characterized by unusually large Rabi splittings, even in the vacuum state. They show the counter-intuitive feature of a lifetime of the lower polariton state longer than for all other excited states. Here we build up a new theoretical framework to understand the dynamics of such coupled system. In particular, we show that the non-Markovian character of the relaxation of the dressed organic system explains the long lifetime of the lower polariton state.

cond-mat.mes-hall↗

arXiv2013

Generating far-field orbital angular momenta from near-field optical chirality

We demonstrate that nanostructures carefully designed on both sides of a thin suspended metallic membrane couple light into a chiral near field and transmit vortex beams through a central aperture that connects the two sides of the membrane. We show how far-field orbital angular momentum (OAM) indices can be tailored through nanostructure designs. We reveal the crucial importance of OAM selection rules imposed by the central aperture and derive OAM summation rules in perfect agreement with experimental data.

physics.optics↗

arXiv2010

Miniature plasmonic wave plates

Linear birefringence, as implemented in wave plates, is a natural way to control the state of polarization of light. We report on a general method for designing miniature planar wave plates using surface plasmons. The resonant optical device considered here is a single circular aperture surrounded by an elliptical antenna grating. The difference in short and long axis of each ellipses introduces a phase shift on the surface plasmons which enables the realization of a quarter wave plate. Furthermore, the experimental results and the theoretical analysis show that the general procedure used does not influence the optical coherence of the polarization state and allows us to explore completely the surface of the unit Poincare sphere by changing only the shape of the elliptical grating.

physics.optics↗

arXiv2007

Radiative and non-radiative photokinetics alteration inside a single metallic nanometric aperture

We resolve the photokinetic rates enhancement of Rhodamine 6G molecules diffusing in a water-glycerol mixture within a single nanometric aperture milled in an opaque aluminium film. Combining fluorescence correlation spectroscopy and lifetime measurements, we report the relative influence of excitation, radiative and non-radiative decay in the fluorescence process, giving a detailed description of the physics behind the overall 15 fold enhancement of the average fluorescence rate per molecule. This procedure is broadly adaptable to a wide range of nanostructures.

quant-ph↗