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Sökning: WFRF:(Sundqvist Bertil)

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21.
  • Andersson, Göran, et al. (författare)
  • Pressure dependence of the c-axis resistance of stage 2 SbCl5 intercalated graphite to 4 GPa
  • 1988
  • Ingår i: Solid State Communications. - : Elsevier BV. - 0038-1098 .- 1879-2766. ; 65:7, s. 735-738
  • Tidskriftsartikel (refereegranskat)abstract
    • The c-axis electrical resistance R has been measured under pressure up to 4 GPa (40 kbar) at room temperature for stage 2, HOPG-based SbCl5 intercalated graphite. In addition to the well known ordering transition at 0.3–0.5 GPa a second anomaly in R is observed above 1 GPa, corresponding to a further phase transition which is not completed until above 2.4 GPa. In all phases R depends more strongly on p for the intercalated material than for HOPG, and the total decrease in R is over 80% to 4 GPa.
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22.
  • Andersson, Ove, et al. (författare)
  • A low-temperature high-pressure apparatus with a temperature control system
  • 1992
  • Ingår i: High Pressure Research. - : Informa UK Limited. - 0895-7959 .- 1477-2299. ; 10:4, s. 599-606
  • Tidskriftsartikel (refereegranskat)abstract
    • A low-temperature high-pressure apparatus was designed using commercial cryogenic equipment. Pressures up to 1 GPa and temperatures down to 40 K can be obtained in a volume of up to 30 cm3. The apparatus is of the piston-cylinder type with a piston diameter of 45 mm, and the pressure can be varied at all temperatures, An adaptive temperature control system keeps the temperature inside the pressure cylinder constant to within ±0.1 K.
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23.
  • Andersson, Odd E., et al. (författare)
  • A study of temperature and pressure induced structural and electronic changes in SbCl5 intercalated graphite : Part II. Experimental data for c-axis resistivity
  • 1992
  • Ingår i: Journal of Materials Research. - 0884-2914 .- 2044-5326. ; 7:11, s. 2989-3000
  • Tidskriftsartikel (refereegranskat)abstract
    • We present experimental data for the c-axis resistivity ?c of stage s = 2, 3, 4, 5, and 8, SbCl5 intercalated graphite, over the temperature range 40 to 300 K and the pressure range 0 to 0.8 GPa (0–8 kbar). For most specimens studied, resistance anomalies are observed below 230 K at atmospheric pressure and at pressures up to 0.5 GPa at 293 K. These anomalies are explained in terms of structural changes from a disordered or partly crystallized in-plane intercalate structure at atmospheric pressure and T > 230 K to an almost completely crystallized structure below this temperature, or at elevated pressures, as discussed in a companion paper. In the crystallized phases ?c is approximately linear in T except for stage 8, for which a nonlinear behavior, with a negative temperature coefficient of resistivity below 200 K, is observed. The results are compared with previously available literature data, and the p-T phase diagram is briefly discussed.
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24.
  • Andersson, Odd E., et al. (författare)
  • A study of temperature and pressure induced structural and electronic changes in SbCl5 intercalated graphite : Part IV: Basal plane resistivity
  • 1995
  • Ingår i: Journal of Materials Research. - 0884-2914 .- 2044-5326. ; 10:7, s. 1653-1660
  • Tidskriftsartikel (refereegranskat)abstract
    • Using an inductive technique, we have measured the in-plane resistivity rhoa of stages 2, 4, 5, and 8 SbCl5-GIC's versus temperature T and pressure p in the ranges 130–300 K and 0–0.85 GPa. The room temperature values of rhoa range from 4.0 µOcm for the stages 5 sample to 7.7 µOcm for the stage 8 sample. At all pressures, rhoa shows a metallic temperature dependence rhoa ~ Ta, with 1 < a < 2, but in contrast to the c-axis resistivity rhoc, it depends only very weakly on pressure and/or intercalate structural order. We show that the behavior observed is consistent with a band conduction model.
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25.
  • Andersson, Odd E., et al. (författare)
  • C-axis resistance of HgCl2 intercalated graphite as a function of temperature and pressure
  • 1989
  • Ingår i: Synthetic Metals volume 34. - Lausanne : Elsevier Sequoia SA. ; , s. 485-490
  • Konferensbidrag (refereegranskat)abstract
    • The c-axis resistance of stage 3 HgCl2 intercalated graphite has been measured as a function of temperature T and pressure p in the range 40 to 300 K and up to 1 GPa (10 kbar). The absolute resistivity and its T- and p- dependence are all in good agreement with data for other acceptor compounds. The measurements show that a previosly unknown phase transformation occurs above 0.4 GPa. Below 250 K the high pressure phase is metastable down to zero pressure, and an x-ray diffraction analysis of metastable material shows that no stage change occurs. The transition thus probably leads to a different in-plane structure characterized by a more densely packed intercalate layer.
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26.
  • Andersson, Odd E., et al. (författare)
  • Low temperature calibration of Manganin pressure gauges
  • 1997
  • Ingår i: Review of Scientific Instruments. - : AIP Publishing. - 0034-6748 .- 1089-7623. ; 68:2, s. 1344-1345
  • Tidskriftsartikel (refereegranskat)abstract
    • High pressures are often measured using the resistance of Manganin wires. However, the pressure coefficient of resistance is known to depend on temperature. We have measured this temperature dependence by comparing the output from a Manganin gauge with that of a well calibrated Zeranin gauge and determined a correction factor which enables us to measure the pressure at any temperature between 150 and 300 K with a temperature dependent error well below 0.5%.
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27.
  • Andersson, Odd E., et al. (författare)
  • Pressure-induced modifications of structural and transport properties in SbCl5 intercalated graphite
  • 1992
  • Ingår i: Materials Science Forum volumes 91-93, Part I. - Zürich : Trans Tech Publications. - 0878496394 ; , s. 301-306
  • Konferensbidrag (refereegranskat)abstract
    • The structure and the c-axis resistivity of SbCl5 intercalated graphite have been studied as functions of T and p, over the ranges 40 to 295 K and 0 to 0.7 GPa. Slow cooling or slow application of pressure p > 0.4 GPa lead to states of complete but different crystallization of the intercalate, but after rapid cooling or pressurization any crystallization is incomplete. The resistivity of the high pressure crystallized phase is about 50% lower than that of the low T, low p phase under identical p-T conditions. No significant difference is seen between the behaviour of HOPG-based and single crystal based materials.
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28.
  • Andersson, Odd E., et al. (författare)
  • Structure, c-axis resistivity, and p-T phase diagram of SbCl5 intercalated graphite
  • 1989
  • Ingår i: Synthetic Metals volume 34. - Lausanne : Elsevier Sequoia SA. ; , s. 187-192
  • Konferensbidrag (refereegranskat)abstract
    • Experimental data are reported for the c-axis resistivity varrhoc of stages n = 3,4,5 and 8 SbCl5 intercalated graphite as a function of T and p, in the range 40 – 300 K and 0-0.5 GPa (5 kbar). varrhoc varied in a systematic way with p, T, and n. Well ordered low-T phases were obtained for all stages; disordering at 200 – 235 K gave rise to well defined multiple anomalies in varrhoc. We also report x-ray diffraction data on the stage 2 compound: evidence was found for large variations in the in-plane structure even for nominally identical samples.
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29.
  • Andersson, Odd E., et al. (författare)
  • The c-axis resistivity for two HOPG-based, first stage CuAl2Cl8 and second stage CuCl2 - graphite intercalation compounds as a function of both pressure and temperature
  • 1996
  • Ingår i: Journal of Physics and Chemistry of Solids, volume 57, issues 6-8. - : Elsevier Ltd.. ; , s. 719-723
  • Konferensbidrag (refereegranskat)abstract
    • In this paper we present data for the c-axis resistivity of first stage CuAl2Cl8 GIC and second stage CuCl2 GIC as functions of pressure, p, (0.0 < p < 1.5 GPa) and of temperature, T, (4 < T < 300 K). We show evidence of a possible new high-pressure phase above 1.0 GPa for the CuAl2Cl8 GIC and we show that the CuCl2 GIC is very stable at all pressures and temperature investigated. We make a comparison with previous results on SbCl5 GICs and other chloride intercalation compounds and with theories treating the temperature and pressure coefficients of transport parameters in layered solids.
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30.
  • Andersson, Ove, et al. (författare)
  • Phase coexistence and hysteresis effects in the pressure-temperature phase diagram of NH3BH3
  • 2011
  • Ingår i: Physical Review B. Condensed Matter and Materials Physics. - : American Physical Society. - 1098-0121 .- 1550-235X. ; 84:2, s. 024115-
  • Tidskriftsartikel (refereegranskat)abstract
    • The potential hydrogen storage compound NH3BH3 has three known structural phases in the temperature and pressure ranges 110–300 K and 0–1.5 GPa, respectively. We report here the boundaries between, and the ranges of stability of, these phases. The phase boundaries were located by in situ measurements of the thermal conductivity, while the actual structures in selected areas were identified by in situ Raman spectroscopy and x-ray diffraction. Below 0.6 GPa, reversible transitions involving only small hysteresis effects occur between the room-temperature tetragonal plastic crystal I4mm phase and the low-temperature orthorhombic Pmn21 phase. Transformations of the I4mm phase into the high-pressure orthorhombic Cmc21 phase, occurring above 0.8 GPa, are associated with very large hysteresis effects, such that the reverse transition may occur at up to 0.5 GPa lower pressures. Below 230 K, a fraction of the Cmc21 phase is metastable to atmospheric pressure, suggesting the possibility that dense structural phases of NH3BH3, stable at room temperature, could possibly be created and stabilized by alloying or by other methods. Mixed orthorhombic Pmn21/Cmc21 phases were observed in an intermediate pressure-temperature range, but a fourth structural phase predicted by Filinchuk et al. [ Phys. Rev. B 79 214111 (2009)] was not observed in the pressure-temperature ranges of this experiment. The thermal conductivity of the plastic crystal I4mm phase is about 0.6 W m−1 K−1 and only weakly dependent on temperature, while the ordered orthorhombic phases have higher thermal conductivities limited by phonon-phonon scattering.
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