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Electronic structure transformation in small bare Au clusters as seen by x-ray photoelectron spectroscopy

Andersson, T. (författare)
Uppsala University,Uppsala universitet,Molekyl- och kondenserade materiens fysik
Zhang, C. (författare)
Uppsala University,Uppsala universitet,Molekyl- och kondenserade materiens fysik
Björneholm, Olle (författare)
Uppsala University,Uppsala universitet,Molekyl- och kondenserade materiens fysik
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Mikkelä, M. H. (författare)
Oulu Univ, Dept Phys Sci, Box 3000, FI-90014 Oulu, Finland.,University of Oulu
Jankala, K. (författare)
Oulu Univ, Dept Phys Sci, Box 3000, FI-90014 Oulu, Finland.,University of Oulu
Anin, D. (författare)
Oulu Univ, Dept Phys Sci, Box 3000, FI-90014 Oulu, Finland.,University of Oulu
Urpelainen, S. (författare)
Oulu Univ, Dept Phys Sci, Box 3000, FI-90014 Oulu, Finland.,University of Oulu
Huttula, M. (författare)
Oulu Univ, Dept Phys Sci, Box 3000, FI-90014 Oulu, Finland.
Tchaplyguine, M. (författare)
Lund University,Lunds universitet,MAX IV-laboratoriet,MAX IV Laboratory
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 (creator_code:org_t)
2016-12-19
2017
Engelska.
Ingår i: Journal of Physics B. - : IOP Publishing. - 0953-4075 .- 1361-6455. ; 50:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Free bare gold clusters in the size range from few tens to few hundred atoms (<= 1 nm dimensions) have been produced in a beam, and the size-dependent development of their full valence band including the 5d and 6s parts has been mapped 'on the fly' by synchrotron-based photoelectron spectroscopy. The Au 4f core level has been also probed, and the cluster-specific Au 4f ionization energies have been used to estimate the cluster size. The recorded in the present work valence spectra of the small clusters are compared with the spectra of the large clusters (N similar to 10(3)) created by us using a magnetron-based gas aggregation source. The comparison shows a substantially narrower 5d valence band and the decrease in its splitting for gold clusters in the size range of few hundred atoms and below. Our DFT calculations involving the pseudopotential method show that the 5d band width of the ground state increases with the cluster size and by the size N = 20 becomes comparable with the experimental width of the valence photoelectron spectrum. Similar to the earlier observations on supported clusters we interpret our experimental and theoretical results as due to the undercoordination of a large fraction of atoms in the clusters with N similar to 10(2) and below. The consequences of such electronic structure of small gold clusters are discussed in connection with their specific physical and chemical properties related to nanoplasmonics and nanocatalysis.

Ämnesord

NATURVETENSKAP  -- Fysik -- Den kondenserade materiens fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Condensed Matter Physics (hsv//eng)
NATURVETENSKAP  -- Fysik -- Atom- och molekylfysik och optik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Atom and Molecular Physics and Optics (hsv//eng)

Nyckelord

Au 5d valence band
Au 4f core level
free bare clusters
synchrotron radiation
x-ray photoelectron spectroscopy
size-dependent electronic structure
Au 4f core level
Au 5d valence band
free bare clusters
size-dependent electronic structure
synchrotron radiation
x-ray photoelectron spectroscopy

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