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Träfflista för sökning "WFRF:(Andersen J) ;pers:(Nyholm R.)"

Sökning: WFRF:(Andersen J) > Nyholm R.

  • Resultat 1-10 av 66
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1.
  • Nyholm, R., et al. (författare)
  • ADSORPTION-SITE DETERMINATION OF ORDERED YB ON SI(111) SURFACES
  • 1993
  • Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 47:15, s. 9663-9668
  • Tidskriftsartikel (refereegranskat)abstract
    • Low-energy-electron-diffraction (LEED), scanning-tunneling-microscopy (STM), and photoelectron-spectroscopy measurements have been performed on the ordered submonolayer surface reconstructions of Yb on Si(111). Two of these reconstructions, namely, 3 X 1 and 2 X 1, have been studied in detail. STM and LEED revealed that what was considered to be the 3 X 1 reconstruction is actually a 3 X 2 reconstruction. By combining STM and photoelectron-spectroscopy results from the 3 X 2 and 2 X 1 reconstructions, we conclude that the Yb atoms are adsorbed in bridge sites.
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2.
  • Nyholm, R., et al. (författare)
  • ELECTRONIC AND STRUCTURAL-PROPERTIES OF THE CU-BI2CASR2CU2O8 INTERFACE
  • 1991
  • Ingår i: Physica. C, Superconductivity. - 0921-4534 .- 1873-2143. ; 180:1-4, s. 120-123
  • Tidskriftsartikel (refereegranskat)abstract
    • The formation of the Cu-Bi2CaSr2Cu2O8 interface has been studied by photoelectron spectroscopy using synchrotron radiation. Photon energies in the range 20-1000 eV were utilized in order to probe both the valence band and to monitor chemical changes upon Cu deposition, as revealed by the core-level shifts. A strong chemical reaction between Bi2CaSr2CuO8 and Cu is manifested by the formation of metallic Bi. From the intensity variations as a function of electron emission angle it is shown that the metallic Bi segregates to the top surface layer.
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3.
  • Nyholm, R., et al. (författare)
  • EPITAXIAL SILICIDE FORMATION IN THE MG/SI(111) SYSTEM
  • 1993
  • Ingår i: Surface Science. - : Elsevier BV. - 0039-6028 .- 1879-2758. ; 289:3, s. 290-296
  • Tidskriftsartikel (refereegranskat)abstract
    • The silicide formation has been studied in the Mg/Si(111) system by IOW energy electron diffraction (LEED) and photoelectron spectroscopy. It has been found that an epitaxial Mg2Si silicide is responsible for the (2/3 square-root e x 2/3 square-root 3)R30-degrees reconstruction in this system. The thickness of the silicide is limited due to the very low formation temperature for this silicide. The Fermi level is positioned 0.59 +/- 0.06 eV above the valence band maximum in the Si substrate and the valence band maximum in the epitaxial silicide is positioned 0.3 +/- 0.1 eV below the Fermi level.
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4.
  • Nyholm, R., et al. (författare)
  • FORMATION OF SM SILICIDES ON SI(111) - COMPOSITION AND EPITAXY
  • 1993
  • Ingår i: Surface Science. - 0039-6028 .- 1879-2758. ; 293:3, s. 254-259
  • Tidskriftsartikel (refereegranskat)abstract
    • The formation of Sm silicides on Si(111) by means of solid phase epitaxy has been studied with low energy electron diffraction, Auger electron spectroscopy and photoelectron spectroscopy of the Sm 4f level and Si 2p level. A limited reaction is found to occur already at room temperature whereas at higher temperatures a strongly intermixed Sm/Si layer showing some long range order is formed. The Sm atoms of this intermixed phase are found to be completely trivalent in accordance with expectations. The intermixed layer consists of two silicides with different compositions, one of them being SmSi2-x, the other being tentatively ascribed to SmSi.
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5.
  • Nyholm, R., et al. (författare)
  • SURFACE SCIENCE AT MAX-LAB
  • 1989
  • Ingår i: Nuclear Instruments and Methods in Physics Research Section A. - : Elsevier BV. - 0168-9002 .- 1872-9576. ; 282:2-3, s. 553-558
  • Tidskriftsartikel (refereegranskat)
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6.
  • Nyholm, R., et al. (författare)
  • SYNCHROTRON-RADIATION SOFT-X-RAY PHOTOEMISSION-STUDY OF LEAD ON BI2CASR2CU2O8
  • 1992
  • Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 46:10, s. 6488-6494
  • Tidskriftsartikel (refereegranskat)abstract
    • In this paper we present a study of the interaction of Pb with a clean single-crystal Bi2CaSr2Cu2O8 superconductor surface based on photoemission and low-energy electron diffraction (LEED). Deposition of Pb on a Bi2CaSr2Cu2O8 Crystal kept at room temperature gives rise to the formation of metallic Bi and oxidized Pb at the interface. This behavior could not be observed when the crystal was kept at 100 K during Pb deposition. For all investigated Pb overlayers on a cold crystal (100 K), surface-sensitive photoelectron spectroscopy revealed the growth of a covering metallic Pb overlayer film. The growth at 100 K, contrary to the growth at room temperature, preserved the original LEED 5 X 1 pattern even for Pb depositions corresponding to a 24-angstrom thick overlayer indicating epitaxial growth. Furthermore, a rigid 0.4-eV shift of the valence band and the Bi 5d core levels is observed upon initial Pb deposition and is tentatively attributed to electron doping.
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7.
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8.
  • Sandell, A., et al. (författare)
  • Observation of a low-energy adsorbate core-level satellite for CO bonded to palladium : Coordination-dependent effects
  • 1998
  • Ingår i: Physical Review B (Condensed Matter). - 0163-1829. ; 57:20, s. 13199-13208
  • Tidskriftsartikel (refereegranskat)abstract
    • A strong low-energy shake-up satellite for CO adsorbed on Pd is observed. The occurrence of the satellite is established for the CO/1 ML Pd/Mo(110) system at a coverage where CO adsorbs exclusively on-top. Comparisons with CO adsorbed on Pd single-crystal surfaces and small supported Pd particles indicate that the strongly increased satellite intensity is due to the decreased CO-Pd interaction strength for on-top adsorbed CO. This can be used to get further insight into the structure and bonding properties of the adsorbate system. Since a low-energy shake-up feature may be misinterpreted as a chemically shifted component, the conclusion is that great care has to be taken in the evaluation of adsorbate core-level spectra for systems with large variations in adsorption strength depending on the adsorbate sites. Large variations in the CO site distribution may furthermore occur depending on the nature of the Pd substrate: Adsorption of CO on 1 ML Pd/Mo(110) leads to an overlayer dominated by an on-top species and, likewise, the CO overlayer formed on small Pd particles after large doses has a large fraction of on-top bonded species. This is in strong contrast to Pd single-crystal surfaces, where CO adsorbed in more highly coordinated sites is abundant.
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9.
  • Sandell, A., et al. (författare)
  • THE INNER VALENCE REGION OF CO ADSORBED ON PD(100)
  • 1994
  • Ingår i: Journal of Physics. - : IOP Publishing. - 0953-8984 .- 1361-648X. ; 26:19, s. 10659-10668
  • Tidskriftsartikel (refereegranskat)abstract
    • The inner valence region of CO/Pd(100) p(2square-root2 x square-root2)R45-degrees has been studied by angular resolved photoemission at the Pd 4d Cooper minimum, and with resonant Auger spectroscopy at photon energies corresponding to the C 1s and O 1s x-ray absorption (XA) maxima of the unoccupied parts of the 2pi*-Pd 4d hybrid (2pi(un)). Previously unobserved inner valence states are revealed in the direct photoemission and are compared with resonant Auger results. The interpretation and assignment of the different spectral features to different main final state configurations are based on energy, symmetry and intensity arguments, as well as comparisons with previous results.
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10.
  • Wassdahl, N., et al. (författare)
  • Soft x-ray emission studies of adsorbates
  • 1992
  • Ingår i: Physical Review Letters. - 0031-9007. ; 69:5, s. 812-815
  • Tidskriftsartikel (refereegranskat)abstract
    • Soft x-ray emission spectroscopy is for the first time applied to surfaces and adsorbates. Surface sensitivity is achieved by employing synchrotron radiation in grazing incidence for the excitation. We present O K emission from adsorbed atomic oxygen on Ni(100) and Cu(100) and molecular CO on Ni(100). The observed spectral features correspond to the occupied 2p partial density of states of the adsorbates.
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