Relevance of thermal disorder in the electronic and spin ultrafast dynamics of iron in the low-perturbation regime
G.M. Pierantozzi, A. De Vita, R. Cucini, A.M. Finardi, T. Pincelli, F. Sirotti, J. Fujii, C. Dri, G. Brajnik, R. Sergo, G. Cautero, G. Panaccione, and G. Rossi
Understanding the ultrafast demagnetization of transition metals requires pump-probe experiments sensitive to the time evolution of the electronic, spin, and lattice thermodynamic baths. By means of time-resolved photoelectron energy and spin-polarization measurements in the low-pump-fluence regime on iron, we disentangle the different dynamics of hot electrons and demagnetization in the subpicosecond and picosecond time range. We observe a broadening of the Fermi-Dirac distribution, following the excitation of nonthermal electrons at specific region of the iron valence band. The corresponding reduction of the spin polarization is remarkably delayed with respect to the dynamics of electronic temperature. The experimental results are corroborated with a microscopic 3-temperature model highlighting the role of thermal disorder in the quenching of the average spin magnetic moment, and indicating Elliot-Yafet type spin-flip scattering as the main mediation mechanism, with a spin-flip probability of 0.1 and a rate of energy exchange between electrons and lattice of 2.5Kfs−1.
Our Research
Sci. Rep., 13, 3882, (2023)
Nd:YAG infrared laser as a viable alternative to excimer laser: YBCO case study
S.K. Chaluvadi, S. Punathum Chalil, F. Mazzola, S. Dolabella, P. Rajak, M. Ferrara, R. Ciancio, J. Fujii, G. Panaccione, G. Rossi & P. Orgiani
We report on the growth and characterization of epitaxial YBa2Cu3O7−δ (YBCO) complex oxide thin films and related heterostructures exclusively by Pulsed Laser Deposition (PLD) and using first harmonic Nd:Y3Al5O12 (Nd:YAG) pulsed laser source (λ = 1064 nm). High-quality epitaxial YBCO thin film heterostructures display superconducting properties with transition temperature ∼ 80 K. Compared with the excimer lasers, when using Nd:YAG lasers, the optimal growth conditions are achieved at a large target-to-substrate distance d. These results clearly demonstrate the potential use of the first harmonic Nd:YAG laser source as an alternative to the excimer lasers for the PLD thin film community. Its compactness as well as the absence of any safety issues related to poisonous gas represent a major breakthrough in the deposition of complex multi-element compounds in form of thin films.
Our Research
Rev. Sci. Instr., 94, 033903, (2023)
Dual pulsed laser deposition system for the growth of complex materials and heterostructures
P. Orgiani, S.K. Chaluvadi, S. Punathum Chalil, F. Mazzola, A. Jana, S. Dolabella, P. Rajak, M. Ferrara, D. Benedetti, A. Fondacaro, F. Salvador, R. Ciancio, J. Fujii, G. Panaccione, I. Vobornik, and G. Rossi
Here, we present an integrated ultra-high-vacuum (UHV) apparatus for the growth of complex materials and heterostructures. The specific growth technique is the Pulsed Laser Deposition (PLD) by means of a dual-laser source based on an excimer KrF ultraviolet and solid-state Nd:YAG infra-red lasers. By taking advantage of the two laser sources—both lasers can be independently used within the deposition chambers—a large number of different materials—ranging from oxides to metals, to selenides, and others—can be successfully grown in the form of thin films and heterostructures. All of the samples can be in situ transferred between the deposition chambers and the analysis chambers by using vessels and holders’ manipulators. The apparatus also offers the possibility to transfer samples to remote instrumentation under UHV conditions by means of commercially available UHV-suitcases. The dual-PLD operates for in-house research as well as user facility in combination with the Advanced Photo-electric Effect beamline at the Elettra synchrotron radiation facility in Trieste and allows synchrotron-based photo-emission as well as x-ray absorption experiments on pristine films and heterostructures.
NFFA Thesis
University of Milan Bachelor's Degree Thesis, (2019)
All-resolved photoemission spectroscopy of Fe(100) and passivated Fe-p(1x1)O surfaces
A.M. Finardi (Supervisors: G. Rossi, I. Vobornik, J. Fujii)
Le proprietà ottiche, elettroniche e magnetiche dei solidi e delle loro superfici dipendono dalla struttura degli stati elettronici entro alcuni eV dal livello di Fermi. I calcoli della struttura elettronica a bande sono efficaci solo nel caso di materiali a bassa interazione elettrone-elettrone (correlazione). L'esperimento e la guida necessaria per lo studio delle proprietà elettroniche dei solidi e delle loro superfici, ed in particolare la spettroscopia di fotoemissione (photoemission spectroscopy - PES) che si basa sulla misura dello spettro energetico degli elettroni emessi da un solido eccitato da un fascio di fotoni monocromatici di energia eccedente la funzione lavoro. La risoluzione dell'angolo di emissione (Angle-resolved photemission spectroscopy - ARPES) permette di avere informazioni sulla legge di dispersione En(k) dello stato elettronico iniziale, mentre la misura del grado di polarizzazione in spin del fascio di elettroni completa il set di numeri quantici, fornendo un dato molto importante per lo studio delle correlazioni elettroniche.
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