arXiv subjects

Etienne Gaufrès

Publications and source records attributed to Etienne Gaufrès.

10 recordsLinked to original sources

arXiv2026

Networking Molecular Quantum Emitters on a Single Chain : From Single to Cooperative Emitters

Engineering light-matter interactions between multiple free-space quantum emitters is a central challenge for scalable quantum photonic technologies. In particular, accessing regimes of coherent emitter-emitter interactions, where several emitters are coupled through a shared electromagnetic environment, is essential for coherent emission and quantum functionalities. Such interactions require precise control over emitter separation and stabilization at sub-wavelength distances, a level of spatial organization that remains extremely difficult to achieve at the molecular scale in solid-state systems. Here we introduce Encoded Quantum Chains (EQC), a one-dimensional architecture in which cooperative radiative behaviour is programmed through spatial encoding of identical molecular emitters. Organic emitters and inert spacer molecules are co-encapsulated inside dielectric boron nitride nanotubes (BNNTs), enabling statistical control of intermolecular spacing from nanometres to micrometres while enforcing dipole alignment and one-dimensional confinement. Time-resolved fluorescence under ambient conditions reveals accelerated radiative decay, enhanced emission rates per emitter, and the emergence of non-mono-exponential dynamics as spacing falls below the optical wavelength, consistent with cooperative radiative states in one dimension. Bundling of EQCs enables coupling between emitters in neighbouring BNNTs, driving a dimensional crossover toward higher-dimensional delocalisation of the excitation. This modular building-block approach provides a scalable route to engineer light-matter interactions and many-body optical phenomena in confined molecular systems, opening new opportunities for distributed single-photon sources, programmable quantum emitters, and photonic architectures for quantum technologies.

cond-mat.mtrl-sci↗

arXiv2024

Collective states of α-sexithiophene chains inside boron nitride nanotubes

Nanotubes align molecules into one dimensional chains creating collective states through the coupling of the molecular transition dipole moments. These collective excitations have strong fluorescence, narrow bandwidth, and shifted emission/absorption energies. We study the optical properties of α-sexithiophene chains in boron nitride nanotubes by combining fluorescence with far- and near-field absorption spectroscopy. The inner nanotube diameter determines the number of encapsulated molecular chains. A single chain of α-sexithiophene molecules has an optical absorption and emission spectrum that is red-shifted by almost 300 meV compared to the monomer emission, which is much larger than expected from dipole-dipole coupling. The collective state splits into excitation and emission channels with a Stokes shift of 200 meV for chains with two or more files. Our study emphasises the formation of a delocalized collective state through Coulomb coupling of the transition moments that shows a remarkable tuneability in transition energy.

physics.atm-clus↗

arXiv2022

Quantum well confinement and competitive radiative pathways in the luminescence of black phosphorus layers

Black phosphorus (BP) stands out from other 2D materials by the wide amplitude of the band-gap energy (Delta(Eg)) that sweeps an optical window from Visible (VIS) to Infrared (IR) wavelengths, depending on the layer thickness. This singularity made the optical and excitonic properties of BP difficult to map. Specifically, the literature lacks in presenting experimental and theoretical data on the optical properties of BP on an extended thickness range. Here we report the study of an ensemble of photoluminescence spectra from 79 passivated BP flakes recorded at 4 K with thicknesses ranging from 4 nm to 700 nm, obtained by mechanical exfoliation. We observe that the exfoliation steps induce additional defects states that compete the radiative recombination from bound excitons observed in the crystal. We also show that the evolution of the photoluminescence energy versus thickness follows a quantum well confinement model appreciable from a thickness predicted and probed at 25 nm. The BP slabs placed in different 2D heterostructures show that the emission energy is not significantly modulated by the dielectric environment. Introduction Confinement effects

cond-mat.mes-hall↗

arXiv2020

Excitons in bulk black phosphorus evidenced by photoluminescence at low temperature

Atomic layers of Black Phosphorus (BP) present unique opto-electronic properties dominated by a direct tunable bandgap in a wide spectral range from visible to mid-infrared. In this work, we investigate the infrared photoluminescence of BP single crystals at very low temperature. Near-bandedge recombinations are observed at 2 K, including dominant excitonic transitions at 0.276 eV and a weaker one at 0.278 eV. The free-exciton binding energy is calculated with an anisotropic Wannier-Mott model and found equal to 9.1 meV. On the contrary, the PL intensity quenching of the 0.276 eV peak at high temperature is found with a much smaller activation energy, attributed to the localization of free excitons on a shallow impurity. This analysis leads us to attribute respectively the 0.276 eV and 0.278 eV PL lines to bound excitons and free excitons in BP. As a result, the value of bulk BP bandgap is refined to 0.287 eV at 2K.

cond-mat.mes-hall↗

arXiv2015

Phonon-Induced Transparency in Functionalized Single Layer Graphene

Herein, intervalley scattering is exploited to account for anomalous antiresonances in the infrared spectra of doped and disordered single layer graphene. We present infrared spectroscopy measurements of graphene grafted with iodophenyl moieties in both reflection microscopy and transmission configurations. Asymmetric transparency windows at energies corresponding to phonon modes near the Γ and K points are observed, in contrast to the featureless spectrum of pristine graphene. These asymmetric antiresonances are demonstrated to vary as a function of the chemical potential. We propose a model which involves coherent intraband scattering with defects and phonons, thus relaxing the optical selection rule forbidding access to ${\bf q} \neq$ Γ phonons. This interpretation of the new phenomenon is supported by our numerical simulations that reproduce the experimental features.

cond-mat.mes-hall↗

arXiv2015

Light Emission in Silicon from Carbon Nanotubes

The use of optics in microelectronic circuits to overcome the limitation of metallic interconnects is more and more considered as a viable solution. Among future silicon compatible materials, carbon nanotubes are promising candidates thanks to their ability to emit, modulate and detect light in the wavelength range of silicon transparency. We report the first integration of carbon nanotubes with silicon waveguides, successfully coupling their emission and absorption properties. A complete study of this coupling between carbon nanotubes and silicon waveguides was carried out, which led to the demonstration of the temperature-independent emission from carbon nanotubes in silicon at a wavelength of 1.3 μm. This represents the first milestone in the development of photonics based on carbon nanotubes on silicon.

physics.optics↗

arXiv2015

Electroabsorption study of index-defined semiconducting carbon nanotubes

Electroabsorption spectroscopy of well-identified index-defined semiconducting carbon nanotubes is reported. The measurement of high definition electroabsorption spectra allows direct indexation with unique nanotube chirality. Results show that at least for a limited range of diameters, electroabsorption is directly proportional to the exciton binding energy of nanotubes. Electroabsorption is a powerful technique which directly probes into carbon nanotube excitonic states, and may become a useful tool for in situ study of excitons in future nanotube-based photonic devices such as electroabsorption modulators.

cond-mat.mtrl-sci↗

arXiv2010

Optical Gain in Carbon Nanotubes

Semiconducting single-wall carbon nanotubes (s-SWNTs) have proved to be promising material for nanophotonics and optoelectronics. Due to the possibility of tuning their direct band gap and controlling excitonic recombinations in the near-infrared wavelength range, s-SWNT can be used as efficient light emitters. We report the first experimental demonstration of room temperature intrinsic optical gain as high as 190 cm-1 at a wavelength of 1.3 μm in a thin film doped with s-SWNT. These results constitute a significant milestone toward the development of laser sources based on carbon nanotubes for future high performance integrated circuits.

physics.optics↗

arXiv2010

Optical microcavity with semiconducting single-wall carbon nanotubes

We report studies of optical Fabry-Perot microcavities based on semiconducting single-wall carbon nanotubes with a quality factor of 160. We experimentally demonstrate a huge photoluminescence signal enhancement by a factor of 30 in comparison with the identical film and by a factor of 180 if compared with a thin film containing non-purified (8,7) nanotubes. Futhermore, the spectral full-width at half-maximum of the photo-induced emission is reduced down to 8 nm with very good directivity at a wavelength of about 1.3 $μ$m. Such results prove the great potential of carbon nanotubes for photonic applications.

cond-mat.mtrl-sci↗

arXiv2010

Enhancement of semiconducting single-wall carbon nanotubes photoluminescence

Photoluminescence properties of semiconducting single wall carbon nanotubes (s-SWNT) thin films with different metallic single wall carbon nanotubes (m-SWNT) concentrations are reported. s-SWNT purified samples are obtained by polymer assisted selective extraction. We show that a few m-SWNT in the sample generates a drastic quenching of the emission. Therefore, highly purified s-SWNT films are a strongly luminescent material and a good candidate for future applications in photonics, such as near infrared emitters, modulators and detectors.

cond-mat.mtrl-sci↗