We present spatially resolved spectral mode mapping of resonant plasmon gap antennas using two-photon luminescence microspectroscopy. The obtained maps are in good agreement with 3D calculations of the antenna modes. The evolution of the modal field with wavelength, both in the gap and along the two coupled gold nanowires forming the antenna, is directly visualized. At resonance, the luminescence for the gap area is enhanced at least 80 times and a comparison with the antenna extremities shows a dynamical charge redistribution due to the near-field coupling between the two arms.
Immobilizing individual living microorganisms at designated positions in space is important to study their metabolism and to initiate an in situ scrutiny of the complexity of life at the nanoscale. While optical tweezers enable the trapping of large cells at the focus of a laser beam, they face difficulties in maintaining them steady and can become invasive and produce substantial damage that prevents preserving the organisms intact for sufficient time to be studied. Here we demonstrate a novel optical trapping scheme that allows us to hold living Escherichia coli bacteria for several hours using moderate light intensities. We pattern metallic nanoantennas on a glass substrate to produce strong light intensity gradients responsible for the trapping mechanism. Several individual bacteria are trapped simultaneously with their orientation fixed by the asymmetry of the antennas. This unprecedented immobilization of bacteria opens an avenue toward observing nanoscopic processes associated with cell metabolism, as well as the response of individual live microorganisms to external stimuli, much in the same way as pluricellular organisms are studied in biology.
Tailoring the light-matter interaction and the local density of optical states (LDOS) with nanophotonics provides accurate control over the luminescence properties of a single quantum emitter. This paradigm is also highly attractive to enhance the near-field Förster resonance energy transfer (FRET) between two fluorescent emitters. Despite the wide applications of FRET in nanosciences, using nanophotonics to enhance FRET has remained a debated and complex challenge. Here we demonstrate enhanced energy transfer within single donor-acceptor fluorophore pairs confined in single gold nanoapertures. Experiments monitoring both the donor and the acceptor emission photodynamics clearly establish a linear dependence of the FRET rate on the LDOS in nanoapertures, demonstrating that nanophotonics can be used to intensify the near-field energy transfer. Strikingly, we observe a significant six-fold increase in the FRET rate for large donor-acceptor separations exceeding 13 nm. Exciting opportunities are opened to investigate biochemical structures with donor-acceptor distances much beyond the classical Förster radius. Importantly, our approach is fully compatible with the detection of single biomolecules freely diffusing in water solution under physiological conditions.
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