Ivana Vobornik is activity coordinator of APE LOW ENERGY synchrotron radiation beamline.
Her research interests are centered on photoelectron spectroscopies with conventional and synchrotron radiation sources, ultra-high vacuum (UHV) techniques, UHV compatible surface preparation techniques and thin film deposition; Auger electron spectroscopy; low energy electron diffraction (LEED), Laue X-ray diffraction; resistivity and susceptibility measurements.
We investigate the temperature-dependent electronic structure of the van der Waals ferromagnet, CrGeTe3. Using angle-resolved photoemission spectroscopy, we identify atomic- and orbital-specific band shifts upon cooling through TC. From these, together with x-ray absorption spectroscopy and x-ray magnetic circular dichroism measurements, we identify the states created by a covalent bond between the Te 5p and the Cr eg orbitals as the primary driver of the ferromagnetic ordering in this system, while it is the Cr t2g states that carry the majority of the spin moment. The t2g states furthermore exhibit a marked bandwidth increase and a remarkable lifetime enhancement upon entering the ordered phase, pointing to a delicate interplay between localized and itinerant states in this family of layered ferromagnets.
From our users
J. Phys. Soc. JPN, 89, 044711, (2020)
Electronic Structure of Yb(Ni1−xCox)3Ga9 Studied by Angle-resolved Photoelectron Spectroscopy
Y. Utsumi, D. Mondal, J. Fujii, I. Vobornik, S. Nakamura, D. Matković-Čalogović, and S. Ohara
Chiral crystal YbNi3Ga9 is known as an intermediate valence compound in which a strong hybridization between the 4f orbitals and the conduction band is present. The Co-substitution to YbNi3Ga9 works as a hole doping that reduces the Kondo temperature and enhances the effective mass of itinerant charge carriers. Using angle-resolved photoelectron spectroscopy, the complex band structure of Yb(Ni1−xCox)3Ga9 (x=0,0.1) is revealed. A Yb2+ 4f7/2 band and evidences of hybridization to valence bands are found near the Fermi level. Both YbNi3Ga9 and the Co-substituted compound exhibit double hexagonal Fermi surfaces centered at the Γ¯-point, surrounded by a large snowflake-like surface, and a triangular electron-like surface along the Γ¯M¯ direction. By changing the incident photon energy, the band dispersion along the c-axis and the barrel-shaped Fermi surface is observed.
Phys. Rev. Materials, 4, 025801, (2020)
Distinct behavior of localized and delocalized carriers in anatase TiO2 (001) during reaction with O2
C. Bigi, Z. Tang, G.M. Pierantozzi, P. Orgiani, P. K. Das, J. Fujii, I. Vobornik, T. Pincelli, A. Troglia, T.-L. Lee, R. Ciancio, G. Drazic, A. Verdini, A. Regoutz, P.D.C. King, D. Biswas, G. Rossi, G. Panaccione, and A. Selloni
Two-dimensional (2D) metallic states induced by oxygen vacancies (VOs) at oxide surfaces and interfaces provide opportunities for the development of advanced applications, but the ability to control the behavior of these states is still limited. We used angle resolved photoelectron spectroscopy combined with density-functional theory (DFT) to study the reactivity of VO-induced states at the (001) surface of anatase TiO2, where both 2D metallic and deeper lying in-gap states (IGs) are observed. The 2D and IG states exhibit remarkably different evolutions when the surface is exposed to molecular O2: while IGs are almost completely quenched, the metallic states are only weakly affected. DFT calculations indeed show that the IGs originate from surface VOs and remain localized at the surface, where they can promptly react with O2. In contrast, the metallic states originate from subsurface vacancies whose migration to the surface for recombination with O2 is kinetically hindered on anatase TiO2 (001), thus making them much less sensitive to oxygen dosing.
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NFFA is a Progetto Internazionale financed by MIUR through CNR
(Istituto Officina dei Materiali, Trieste) and Elettra-Sincrotrone Trieste
and managed by the Commissione NFFA chaired by Giorgio Rossi
(Università di Milano and IOM-CNR).