Time-Resolved XUV Absorption Spectroscopy and Magnetic Circular Dichroism at the Ni <i>M</i><sub>2,3</sub>-Edges

Ultrashort optical pulses can trigger a variety of non-equilibrium processes in magnetic thin films affecting electrons and spins on femtosecond timescales. In order to probe the charge and magnetic degrees of freedom simultaneously, we developed an X-ray streaking technique that has the advantage o...

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Main Authors: Marcel Hennes, Benedikt Rösner, Valentin Chardonnet, Gheorghe S. Chiuzbaian, Renaud Delaunay, Florian Döring, Vitaliy A. Guzenko, Michel Hehn, Romain Jarrier, Armin Kleibert, Maxime Lebugle, Jan Lüning, Gregory Malinowski, Aladine Merhe, Denys Naumenko, Ivaylo P. Nikolov, Ignacio Lopez-Quintas, Emanuele Pedersoli, Tatiana Savchenko, Benjamin Watts, Marco Zangrando, Christian David, Flavio Capotondi, Boris Vodungbo, Emmanuelle Jal
Format: Article
Language:English
Published: MDPI AG 2020-12-01
Series:Applied Sciences
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Online Access:https://www.mdpi.com/2076-3417/11/1/325
Description
Summary:Ultrashort optical pulses can trigger a variety of non-equilibrium processes in magnetic thin films affecting electrons and spins on femtosecond timescales. In order to probe the charge and magnetic degrees of freedom simultaneously, we developed an X-ray streaking technique that has the advantage of providing a jitter-free picture of absorption cross-section changes. In this paper, we present an experiment based on this approach, which we performed using five photon probing energies at the Ni <inline-formula><math display="inline"><semantics><msub><mi>M</mi><mrow><mn>2</mn><mo>,</mo><mn>3</mn></mrow></msub></semantics></math></inline-formula>-edges. This allowed us to retrieve the absorption and magnetic circular dichroism time traces, yielding detailed information on transient modifications of electron and spin populations close to the Fermi level. Our findings suggest that the observed absorption and magnetic circular dichroism dynamics both depend on the extreme ultraviolet (XUV) probing wavelength, and can be described, at least qualitatively, by assuming ultrafast energy shifts of the electronic and magnetic elemental absorption resonances, as reported in recent work. However, our analysis also hints at more complex changes, highlighting the need for further experimental and theoretical studies in order to gain a thorough understanding of the interplay of electronic and spin degrees of freedom in optically excited magnetic thin films.
ISSN:2076-3417