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    Stable laser-ion acceleration in the light sail regime
    (College Park : American Institute of Physics Inc., 2013) Steinke, S.; Hilz, P.; Schnürer, M.; Priebe, G.; Bränzel, J.; Abicht, F.; Kiefer, D.; Kreuzer, C.; Ostermayr, T.; Schreiber, J.; Andreev, A.A.; Yu, T.P.; Pukhov, A.; Sandner, W.
    We present experimental results on ion acceleration with circularly polarized, ultrahigh contrast laser pulses focused to peak intensities of 5×1019 W cm-2 onto polymer targets of a few 10 nanometer thickness. We observed spatially and energetically separated protons and carbon ions that accumulate to pronounced peaks around 2 MeV containing as much as 6.5% of the laser energy. Based on particle-in-cell simulation, we illustrate that an early separation of heavier carbon ions and lighter protons creates a stable interface that is maintained beyond the end of the radiation pressure dominated acceleration process.
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    Tailoring optical properties and stimulated emission in nanostructured polythiophene
    ([London] : Macmillan Publishers Limited, part of Springer Nature, 2019) Portone, Alberto; Ganzer, Lucia; Branchi, Federico; Ramos, Rodrigo; Caldas, Marília J.; Pisignano, Dario; Molinari, Elisa; Cerullo, Giulio; Persano, Luana; Prezzi, Deborah; Virgili, Tersilla
    Polythiophenes are the most widely utilized semiconducting polymers in organic electronics, but they are scarcely exploited in photonics due to their high photo-induced absorption caused by interchain polaron pairs, which prevents the establishment of a window of net optical gain. Here we study the photophysics of poly(3-hexylthiophene) configured with different degrees of supramolecular ordering, spin-coated thin films and templated nanowires, and find marked differences in their optical properties. Transient absorption measurements evidence a partially-polarized stimulated emission band in the nanowire samples, in contrast with the photo-induced absorption band observed in spin-coated thin films. In combination with theoretical modeling, our experimental results reveal the origin of the primary photoexcitations dominating the dynamics for different supramolecular ordering, with singlet excitons in the nanostructured samples superseding the presence of polaron pairs, which are present in the disordered films. Our approach demonstrates a viable strategy to direct optical properties through structural control, and the observation of optical gain opens the possibility to the use of polythiophene nanostructures as building blocks of organic optical amplifiers and active photonic devices. © 2019, The Author(s).