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Author: Ciappina, Marcelo F. × Version: publishedVersion ×

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    Quantum-Optical Spectrometry in Relativistic Laser-Plasma Interactions Using the High-Harmonic Generation Process: A Proposal
    (Basel : MDPI, 2021) Lamprou, Theocharis; Lopez-Martens, Rodrigo; Haessler, Stefan; Liontos, Ioannis; Kahaly, Subhendu; Rivera-Dean, Javier; Stammer, Philipp; Pisanty, Emilio; Ciappina, Marcelo F.; Lewenstein, Maciej; Tzallas, Paraskevas
    Quantum-optical spectrometry is a recently developed shot-to-shot photon correlation-based method, namely using a quantum spectrometer (QS), that has been used to reveal the quantum optical nature of intense laser–matter interactions and connect the research domains of quantum optics (QO) and strong laser-field physics (SLFP). The method provides the probability of absorbing photons from a driving laser field towards the generation of a strong laser–field interaction product, such as high-order harmonics. In this case, the harmonic spectrum is reflected in the photon number distribution of the infrared (IR) driving field after its interaction with the high harmonic generation medium. The method was implemented in non-relativistic interactions using high harmonics produced by the interaction of strong laser pulses with atoms and semiconductors. Very recently, it was used for the generation of non-classical light states in intense laser–atom interaction, building the basis for studies of quantum electrodynamics in strong laser-field physics and the development of a new class of non-classical light sources for applications in quantum technology. Here, after a brief introduction of the QS method, we will discuss how the QS can be applied in relativistic laser–plasma interactions and become the driving factor for initiating investigations on relativistic quantum electrodynamics.
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    All-optical spatio-temporal control of electron emission from SiO2 nanospheres with femtosecond two-color laser fields
    ([London] : IOP, 2019) Liu, Qingcao; Zherebtsov, Sergey; Seiffert, Lennart; Skruszewicz, Slawomir; Zietlow, Dominik; Ahn, Seongjin; Rupp, Philipp; Wnuk, Pawel; Sun, Shaohua; Kessel, Alexander; Trushin, Sergei; Schlander, Annika; Kim, Dongeon; Rühl, Eckart; Ciappina, Marcelo F.; Tiggesbäumker, Josef; Gallei, Markus; Fennel, Thomas; Kling1, Matthias F.
    Field localization by nanostructures illuminated with laser pulses of well-defined waveform enables spatio-temporal tailoring of the near-fields for sub-cycle control of electron dynamics at the nanoscale. Here, we apply intense linearly-polarized two-color laser pulses for all-optical control of the highest energy electron emission from SiO2 nanoparticles. For the size regime where light propagation effects become important, we demonstrate the possibility to control the preferential emission angle of a considerable fraction of the fastest electrons by varying the relative phase of the two-color field. Trajectory based semi-classical simulations show that for the investigated nanoparticle size range the directional steering can be attributed to the two-color effect on the electron trajectories, while the accompanied modification of the spatial distribution of the ionization rate on the nanoparticle surface has only a minor effect. © 2019 The Author(s). Published by IOP Publishing Ltd on behalf of the Institute of Physics and Deutsche Physikalische Gesellschaft