arXiv subjects

Jérémie Béal

Publications and source records attributed to Jérémie Béal.

3 recordsLinked to original sources

arXiv2026

Absolute measurement of the intrinsic helicity in nanophotonics

Helicity is a universal quantity describing the internal rotation of an object or a field. Whether it characterizes fundamental properties such as the spin of elementary particles or leads to practical consequences such as the toxicity or harmlessness of chiral molecules, defining and measuring it is essential. However, this remains ambiguous in the case of chiral photonic systems such as plasmonic nanoparticles or photonic metasurfaces, where contrary to common knowledge, the observation of circularly polarized dependent optical properties is not a relevant measure for the helicity. We demonstrate experimentally and theoretically that the helicity can be rigorously defined and measured in a nanophotonic system emitting circularly polarized light after excitation in the near-field by a focused electron beam. In the case of a model system composed of two plasmonic dipoles (Born-Kuhn systems), we show that the helicity of photonic modes takes on a very intuitive form and can be simply measured by symmetrizing the geometry of excitation and detection. The method could be extended to a variety of chiral photonic systems, whose locally enhanced properties make them promising for the engineering of local chirality.

physics.optics↗

arXiv2021

Band-edge emission enhancement in sputtered ZnO thin films with ultraviolet surface lattice resonances

Metallic nanostructures acting as optical nanoantennas can significantly enhance the photoluminescence (PL) of nearby emitters. Albeit luminescence enhancement factors of several orders of magnitude have been reported for quantum dots or molecules, in the case of bulk emitters the magnitude of the plasmonic enhancement is strongly hindered by the weak spatial overlap between the active medium and the electromagnetic modes of the nanoantenna. Here, we propose a solid-state ultraviolet emitter based on a thin film of zinc oxide (ZnO) coupled with an array of aluminum (Al) nanoparticles. The Al nanorod array is designed to sustain surface lattice resonances (SLRs) in the near ultraviolet, which are hybrid modes exhibiting a Fano-like lineshape with narrowed linewidth relatively to the non-hybridized plasmonic modes. By changing both the period of the array and the dimensions of the nanorods, the generated SLR is tuned either to the near band-edge (NBE) emission of ZnO or to the excitation wavelength. We experimentally demonstrate that NBE emission can be increased up to a factor of 3 compared to bare ZnO. The underlying PL enhancement mechanisms are experimentally investigated and compared with numerical simulations. We also demonstrate that SLRs are more efficient for the ZnO luminescence enhancement compared to localized surface plasmon resonances.

physics.optics↗

arXiv2021

Local Optical Chirality Induced by Near-Field Mode Interference in Achiral Plasmonic Metamolecules

When circularly polarized light interacts with a nanostructure, the optical response depends on the geometry of the structure. If the nanostructure is chiral (i.e., it cannot be superimposed on its mirror image), then its optical response, both in near-field and far-field, depends on the handedness of the incident light. In contrast, achiral structures exhibit identical far-field responses for left- and right-circular polarization. Here, we show that a perfectly achiral nanostructure, a plasmonic metamolecule with trigonal D3h symmetry, exhibits a near-field response that is sensitive to the handedness of light. This effect stems from the near-field interference between the different plasmonic modes sustained by the plasmonic metamolecule under circularly polarized light excitation. The local chirality in a plasmonic trimer is then experimentally evidenced with nanoscale resolution using a molecular probe. Our experiments demonstrate that the optical near-field chirality can be imprinted into the photosensitive polymer, turning an optical chirality into a geometrical chirality that can be imaged using atomic force microscopy. These results are of interest for the field of polarization-sensitive photochemistry.

physics.optics↗