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Sökning: WFRF:(Cameron W) > Luleå tekniska universitet

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1.
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2.
  • Bentham, James, et al. (författare)
  • A century of trends in adult human height
  • 2016
  • Ingår i: eLIFE. - : eLife Sciences Publications Ltd. - 2050-084X. ; 5
  • Tidskriftsartikel (refereegranskat)abstract
    • Being taller is associated with enhanced longevity, and higher education and earnings. We reanalysed 1472 population-based studies, with measurement of height on more than 18.6 million participants to estimate mean height for people born between 1896 and 1996 in 200 countries. The largest gain in adult height over the past century has occurred in South Korean women and Iranian men, who became 20.2 cm (95% credible interval 17.5–22.7) and 16.5 cm (13.3– 19.7) taller, respectively. In contrast, there was little change in adult height in some sub-Saharan African countries and in South Asia over the century of analysis. The tallest people over these 100 years are men born in the Netherlands in the last quarter of 20th century, whose average heights surpassed 182.5 cm, and the shortest were women born in Guatemala in 1896 (140.3 cm; 135.8– 144.8). The height differential between the tallest and shortest populations was 19-20 cm a century ago, and has remained the same for women and increased for men a century later despite substantial changes in the ranking of countries.
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3.
  • Chen, W., et al. (författare)
  • Electronic and geometric structure of clean Pt3Ti(111)
  • 1994
  • Ingår i: Physical Review B. - 0163-1829 .- 1095-3795. ; 50:8, s. 5620-5627
  • Tidskriftsartikel (refereegranskat)abstract
    • Photoemission spectra and scanning tunneling microscopy (STM) images of the clean Pt3Ti(111) surface are presented. Grazing-emission core-level spectra show that the topmost layer is pure platinum, modified compared with the Pt(111) surface. The Pt 4f levels at the surface are shifted 0.4 eV toward the Fermi level relative to bulk Pt3Ti while the Pt 4f and Ti 2p levels in the bulk are shifted 0.4 and 1.3 eV to higher binding energy relative to pure bulk platinum and titanium, respectively, Tunneling measurements show a surface with only metallic atoms and a small p(2×2) buckling. Our observations of molecularly adsorbed CO are not compatible with metallic titanium atoms at the surface and the STM data thus indirectly confirm that only platinum atoms are present in the topmost layer. Linear muffin-tin-orbital calculations of the bulk band structure and valence-band photoemission spectra reveal highly hybridized electron states between the Pt d and Ti d levels. The calculations give a minor charge transfer from Ti to Pt, 0.37 electrons per Ti atom, but the large core-level shifts reflect the stability of the alloy and the response to the excitation rather than the amount of charge transfer. The observed segregation of platinum to the surface and the altered electronic structure of the topmost layer, due to interaction with the underlying alloy, are in full agreement with earlier conclusions based on low-energy electron-diffraction measurements and on the chemical properties of the surface. © 1994 The American Physical Society.
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4.
  • Chen, W., et al. (författare)
  • Redox properties of titanium oxides on Pt3Ti
  • 1995
  • Ingår i: Journal of Physical Chemistry. - : American Chemical Society (ACS). - 0022-3654 .- 1541-5740. ; 99:34, s. 12892-12895
  • Tidskriftsartikel (refereegranskat)abstract
    • The morphology and electronic structure of surface-segregated titanium oxides on Pt3Ti(111) are presented. Core level photoemission spectra at grazing emission reveal two states of oxidation: a dominant and reducible four-valent oxide together with a small amount of a three-valent oxide is produced by oxidation in 0 2 at and below 400°C; an irreducible three-valent oxide by oxidation in 02 at and above 450 °C. The ratio between the active four-valent and the inactive three-valent oxides decreases with increasing oxidation temperature. The probability for reduction by CO is almost unity for the Ti 4+ oxide, and the conclusion must be that the four-valent oxide plays an active role for catalytic reactions. Scanning tunneling measurements relate these observations to changes in the dispersion and nucleation of the oxide overlayer. The four-valent oxide grows as islands with remaining areas open for CO adsorption while the three-valent oxide spreads on and blocks the crystal surface. Photoemission spectra relate these dispersion effects to an electronic interaction between the Ti 3+ oxide and adjacent Pt atoms. The above observations are in accordance with the common picture of dispersion effects in titania-supported SMSI catalysts and prove that interfacial energies play a crucial role whether the dominant phase is metallic or an oxide.
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5.
  • Chen, W., et al. (författare)
  • Structure determination of Pt3Ti(111) by automated tensor LEED
  • 1993
  • Ingår i: Journal of Physics. - : IOP Publishing. - 0953-8984 .- 1361-648X. ; 5, s. 4585-4594
  • Tidskriftsartikel (refereegranskat)abstract
    • An analysis of low-energy electron diffraction (LEED) I-V spectra from the clean Pt3Ti(111) surface was performed by comparing measured intensities with data calculated using an automated tensor LEED program, which employs a directed search optimization procedure. It was found that the topmost layer is pure Pt and that the other layers have the bulk composition. The first and second interlayer spacings are 2.23+or-0.03 AA and 2.21+or-0.03 AA respectively, corresponding to a contraction of 0.9% and 1.8% of the bulk value. The perpendicular buckling is 0.04 AA +or-0.05 AA in the top layer and 0.15 AA +or-0.04 AA in the second layer. The results are in full accordance with previous investigations of the physical and chemical properties of this surface.
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