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Jean-Baptiste Marceau

Publications and source records attributed to Jean-Baptiste Marceau.

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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

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