Correlated electronic decay in expanding clusters triggered by intense XUV pulses from a Free-Electron-Laser

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Tim Oelze
Bernd Schütte
Maria Müller
Jan P. Müller
Marek Wieland
Ulrike Frühling
Markus Drescher
Alaa Al-Shemmary
Torsten Golz
Nikola Stojanovic
Maria Krikunova
机构
[1] Institut für Optik und Atomare Physik,Department of Physics
[2] Technische Universität Berlin,undefined
[3] Max-Born-Institut,undefined
[4] Imperial College London,undefined
[5] South Kensington Campus,undefined
[6] Institut für Optik und Atomare Physik,undefined
[7] Technische Universität Berlin,undefined
[8] Institut für Experimentalphysik,undefined
[9] Universität Hamburg,undefined
[10] Center for Ultrafast Imaging,undefined
[11] Deutsches Elektronen-Synchrotron DESY,undefined
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摘要
Irradiation of nanoscale clusters and large molecules with intense laser pulses transforms them into highly-excited non- equilibrium states. The dynamics of intense laser-cluster interaction is encoded in electron kinetic energy spectra, which contain signatures of direct photoelectron emission as well as emission of thermalized nanoplasma electrons. In this work we report on a so far not observed spectrally narrow bound state signature in the electron kinetic energy spectra from mixed Xe core - Ar shell clusters ionized by intense extreme-ultraviolet (XUV) pulses from a free-electron-laser. This signature is attributed to the correlated electronic decay (CED) process, in which an excited atom relaxes and the excess energy is used to ionize the same or another excited atom or a nanoplasma electron. By applying the terahertz field streaking principle we demonstrate that CED-electrons are emitted at least a few picoseconds after the ionizing XUV pulse has ended. Following the recent finding of CED in clusters ionized by intense near-infrared laser pulses, our observation of CED in the XUV range suggests that this process is of general relevance for the relaxation dynamics in laser produced nanoplasmas.
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