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Dissecting Mott and charge-density wave dynamics in the photoinduced phase of 1T-TaS[sub]2
Alberto Simoncig, Matija Stupar, Barbara Ressel, Tanusree Saha, Primož Rebernik Ribič, Giovanni De Ninno, 2021, original scientific article

Abstract: The two-dimensional transition-metal dichalcogenide 1T−TaS2 is a complex material standing out for its puzzling low temperature phase marked by signatures amenable to both Mott-insulating and charge-density wave states. Electronic Mott states, coupled to a lattice, respond to coherent optical excitations via a modulation of the lower (valence) Hubbard band. Such dynamics is driven by strong electron-phonon coupling and typically lasts for tens of picoseconds, mimicking coherent structural distortions. Instead, the response occurring at the much faster timescale, mainly dominated by electronic many-body effects, is still a matter of intense research. By performing time- and angle-resolved photoemission spectroscopy, we investigated the photoinduced phase of 1T−TaS2 and found out that its lower Hubbard band promptly reacts to coherent optical excitations by shifting its binding energy towards a slightly larger value. This process lasts for a time comparable to the optical pump pulse length, mirroring a transient change of the onsite Coulomb repulsion energy (U). Such an observation suggests that the correction to the bare value of U, ascribed to the phonon-mediated screening which slightly opposes the Hubbard repulsion, is lost within an interval of a few tens of femtoseconds and can be understood as a fingerprint of electronic states largely decoupled from the lattice. Additionally, these results enforce the hypothesis, envisaged in the current literature, that the transient photoinduced states belong to a sort of crossover phase instead of an equilibrium metallic one.
Keywords: ultrafast phenomena, time resolved photoemission, strongly correlated systems, transition metal dichalcogenide
Published in RUNG: 13.04.2021; Views: 2318; Downloads: 0
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3.
Photoelectric effect with a twist
Giovanni De Ninno, Jonas Wätzel, Primož Rebernik Ribič, Enrico Allaria, Marcello Coreno, Miltcho B. Danailov, Christian David, Alexander Demidovich, Michele Di Fraia, Luca Giannessi, Klaus Hansen, Špela Krušič, Michele Manfredda, Micheal Meyer, Andrej Mihelič, Najmeh Mirian, Oksana Plekan, Barbara Ressel, Benedikt Rösner, Alberto Simoncig, Simone Spampinati, Janez Štupar, Matjaž Žitnik, Marco Zangrando, Carlo Callegari, Jamal Berakdar, 2020, original scientific article

Abstract: Photons have fixed spin and unbounded orbital angular momentum (OAM). While the former is manifested in the polarization of light, the latter corresponds to the spatial phase distribution of its wavefront1. The distinctive way in which the photon spin dictates the electron motion upon light– matter interaction is the basis for numerous well-established spectroscopies. By contrast, imprinting OAM on a mat- ter wave, specifically on a propagating electron, is gener- ally considered very challenging and the anticipated effect undetectable2. In refs. 3,4, the authors provided evidence of OAM-dependent absorption of light by a bound electron. Here, we seek to observe an OAM-dependent dichroic photo- electric effect, using a sample of He atoms. Surprisingly, we find that the OAM of an optical field can be imprinted coher- ently onto a propagating electron wave. Our results reveal new aspects of light–matter interaction and point to a new kind of single-photon electron spectroscopy.
Keywords: FEL, OAM, Photoelectric effect
Published in RUNG: 09.09.2020; Views: 2822; Downloads: 0
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