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Author: Palacios, Alicia Ă— Author: Smirnova, Olga Ă— Start date: 1984 Ă— Type: Text Ă— Publisher: Bristol : IOP Publ. Ă—

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    Roadmap on photonic, electronic and atomic collision physics: I. Light-matter interaction
    (Bristol : IOP Publ., 2019) Ueda, Kiyoshi; Sokell, Emma; Schippers, Stefan; Aumayr, Friedrich; Sadeghpour, Hossein; Burgdörfer, Joachim; Lemell, Christoph; Tong, Xiao-Min; Pfeifer, Thomas; Calegari, Francesca; Palacios, Alicia; Martin, Fernando; Corkum, Paul; Sansone, Giuseppe; Gryzlova, Elena V.; Grum-Grzhimailo, Alexei N.; Piancastelli, Maria Novella; Weber, Peter M.; Steinle, Tobias; Amini, Kasra; Biegert, Jens; Berrah, Nora; Kukk, Edwin; Santra, Robin; Müller, Alfred; Dowek, Danielle; Lucchese, Robert R.; McCurdy, C. William; Bolognesi, Paola; Avaldi, Lorenzo; Jahnke, Till; Schöffler, Markus S.; Dörner, Reinhard; Mairesse, Yann; Nahon, Laurent; Smirnova, Olga; Schlathölter, Thomas; Campbell, Eleanor E.B.; Rost, Jan-Michael; Meyer, Michael; Tanaka, Kazuo A.
    We publish three Roadmaps on photonic, electronic and atomic collision physics in order to celebrate the 60th anniversary of the ICPEAC conference. In Roadmap I, we focus on the light-matter interaction. In this area, studies of ultrafast electronic and molecular dynamics have been rapidly growing, with the advent of new light sources such as attosecond lasers and x-ray free electron lasers. In parallel, experiments with established synchrotron radiation sources and femtosecond lasers using cutting-edge detection schemes are revealing new scientific insights that have never been exploited. Relevant theories are also being rapidly developed. Target samples for photon-impact experiments are expanding from atoms and small molecules to complex systems such as biomolecules, fullerene, clusters and solids. This Roadmap aims to look back along the road, explaining the development of these fields, and look forward, collecting contributions from twenty leading groups from the field. © 2019 IOP Publishing Ltd.
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    A molecular clock for autoionization decay
    (Bristol : IOP Publ., 2017-06-14) Medišauskas, Lukas; Bello, Roger Y.; Palacios, Alicia; González-Castrillo, Alberto; Morales, Felipe; Plimak, Lev; Smirnova, Olga; Martín, Fernando; Ivanov, Misha Yu
    The ultrafast decay of highly excited electronic states is resolved with a molecular clock technique, using the vibrational motion associated to the ionic bound states as a time-reference. We demonstrate the validity of the method in the context of autoionization of the hydrogen molecule, where nearly exact full dimensional ab-initio calculations are available. The vibrationally resolved photoionization spectrum provides a time–energy mapping of the autoionization process into the bound states that is used to fully reconstruct the decay in time. A resolution of a fraction of the vibrational period is achieved. Since no assumptions are made on the underlying coupled electron–nuclear dynamics, the reconstruction procedure can be applied to describe the general problem of the decay of highly excited states in other molecular targets.