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Sökning: WFRF:(Chakarov D V)

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1.
  • Hellsing, B, et al. (författare)
  • Photoinduced desorption of potassium atoms from a two dimensional overlayer on graphite
  • 1997
  • Ingår i: Journal of Chemical Physics. - : AIP Publishing. - 0021-9606 .- 1089-7690. ; 106:3, s. 982-1002
  • Tidskriftsartikel (refereegranskat)abstract
    • We present an experimental and theoretical investigation of K atom desorption from the basal plane of graphite at 83 K induced by low energy photons (3-6 eV). The 2D potassium overlayer is characterized by low energy electron diffraction (LEED), high-resolution electron energy loss spectroscopy (HREELS), thermal desorption spectroscopy (TDS), and work function measurements. At monolayer coverage (5.2 x 10(14) atoms cm(-2)), the dependence of the cross section on photon energy has a threshold at (h) over bar omega approximate to 3.0 eV and rises up to a maximum of 1.8 +/- 0.4 x 10(-20) cm(2) at 4.8 eV. The coverage dependence of the photoyield reflects the existence of two phases of adsorbed K, dilute ionized photo-active and close-packed photo-neutral, respectively. The observed photodesorption is a single-photon, nonthermal event, consistent with a substrate-mediated mechanism. The desorption results from attachment of optically excited hot electrons to the empty 4s state of ionized potassium. The theory predicts in this case a Gaussian line shape of the photoyield vs photon energy. Fitting the model parameters to the experimental data, we determine (i) the energy and slope of the excited state potential energy curve, and (ii) the position and width of the potassium-induced 4s resonance. The present findings combined with other available data for potassium on graphite are used to construct 1D potential energy curves along the surface normal for K+ and K-0. The calculated cross sections for s- and p-polarized Light are in qualitative agreement with the measurements. (C) 1997 American Institute of Physics.
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2.
  • Hellsing, B, et al. (författare)
  • Photoinduced desorption of potassium atoms from graphite
  • 1996
  • Ingår i: Surface Science. - : Elsevier BV. - 0039-6028 .- 1879-2758. ; 363:1-3, s. 247-251
  • Tidskriftsartikel (refereegranskat)abstract
    • We present an experimental and theoretical investigation of desorption of potassium atoms from the basal plane of graphite induced by photons with energies from 2 to 6 eV. The intensity of the photon flux employed in the measurements is low, and the observed photodesorption is a single-photon, non-thermal event. At monolayer coverage the photon-energy dependence of the cross section has a maximum at 4.8 eV. The experimental observations are interpreted in terms of a hot carrier mechanism, which involves attachment of optically excited substrate hot electrons to the empty 4s state of ionized potassium, and then desorption. The theory predicts a Gaussian line shape of the photoyield versus photon energy. Fitting the model parameters to the experimental data, we determine: (i) the potential energy for Gr + K+ and Gr + K-0; and (ii) the position (2.4 eV above the Fermi level) and width (0.15 eV) of the potassium 4s resonance, which is in good agreement with independent experimental observations.
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3.
  • Chakarov, D V, et al. (författare)
  • Photos induced desorption and intercalation of potassium atoms deposited on graphite(0001)
  • 1996
  • Ingår i: Applied Surface Science. - 0169-4332 .- 1873-5584. ; 106, s. 186-192
  • Tidskriftsartikel (refereegranskat)abstract
    • In addition to the photodesorption phenomenon previously observed for single K atoms from a graphite surface covered with a monolayer of potassium we present new results related to the photon stimulated interaction of potassium with graphite, which concerns alternative routes for energy relaxation of the photo excited K adatoms: photoinduced intercalation. The desorption yield has a threshold at h omega approximate to 3 eV and a maximum at h omega(max) approximate to 4.9 eV, Polarization measurements indicate a substrate-mediated mechanism. The coverage dependence suggests that only the ionic 2D, K-phase is photo active. The proposed mechanism includes attachment of photo-generated hot electrons to the K 4s adsorbate resonance of energy E(res). Assuming an analogous excitation process we discuss different mechanisms for the K photo intercalation and possible applications of the photon stimulated doping of carboneous materials at low temperature.
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5.
  • Österlund, Lars, 1967-, et al. (författare)
  • Potassium adsorption on graphite(0001)
  • 1999
  • Ingår i: Surface Science. - 0039-6028 .- 1879-2758. ; 420:2-3, s. 174-189
  • Tidskriftsartikel (refereegranskat)abstract
    • Potassium adsorption on graphite has been studied with emphasis on the two-dimensional K adlayer below one monolayer. Data are presented for the work function versus coverage, high-resolution electron energy loss spectroscopy (HREELS) vibrational spectra of K-adlayers, low energy electron diffraction and ultraviolet photoemission spectroscopy (UPS) spectra at different coverages. The data provide information regarding the vibrational properties of the K-adlayer, the metallization of the adlayer at submonolayer coverages, and the charge transfer from the It adatoms to the graphite substrate. Analysis of the work function, HREELS, and UPS data provides a qualitatively consistent picture of the charge state of the K adatoms, where at low coverages, below a critical coverage theta(c) (theta(c) = 0.2-0.3), the K adatoms are dispersed and (partially) ionized, whereas at theta > theta(c) islands of a metallic 2 x 2 K phase develop that coexist with the dispersed K adatoms up to theta = 1. We show that it is possible to understand the variation of the work function data based on a two-phase model without invoking a depolarization mechanism of adjacent dipoles, as is normally done for alkali-metal adsorption on metal surfaces. Similarly, the intensity variation as a function of coverage of the energy loss peak at 17 meV observed in HREELS, and the photoemission peak at E-b = 0.5 eV seen in UPS can be understood from a two-phase model. A tentative explanation is presented that connects apparent discrepancies in the literature concerning the electronic structure of the K adlayer. In particular, a new assignment of the K-induced states near the Fermi level is proposed. (C) 1999 Elsevier Science B.V. All rights reserved.
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