| 1. |
- Adcox, K, et al.
(författare)
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Formation of dense partonic matter in relativistic nucleus-nucleus collisions at RHIC: Experimental evaluation by the PHENIX Collaboration
- 2005
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Ingår i: Nuclear Physics, Section A. - : Elsevier BV. - 0375-9474. ; 757:1-2, s. 184-283
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Forskningsöversikt (refereegranskat)abstract
- Extensive experimental data from high-energy nucleus-nucleus collisions were recorded using the PHENIX detector at the Relativistic Heavy Ion Collider (RHIC). The comprehensive set of measurements from the first three years of RHIC operation includes charged particle multiplicities, transverse energy, yield ratios and spectra of identified hadrons in a wide range of transverse momenta (PT), elliptic flow, two-particle correlations, nonstatistical fluctuations, and suppression of particle production at high PT. The results are examined with an emphasis on implications for the formation of a new state of dense matter. We find that the state of matter created at RHIC cannot be described in terms of ordinary color neutral hadrons.
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| 2. |
- Wang, Lin, et al.
(författare)
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Synthesis and high pressure induced amorphization of C60 nanosheets
- 2007
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Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 91:10, s. 103112-
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Tidskriftsartikel (refereegranskat)abstract
- C-60 nanosheets with thicknesses in the nanometer range were synthesized by a simple method. Compared to bulk C-60, the lattice of the nanosheets is expanded by about 0.4%. In situ Raman spectroscopy and energy-dispersive x-ray diffraction under high pressures have been employed to study the structure of the nanosheets. The studies indicate that the bulk modulus of the C-60 nanosheets is significantly larger than that of bulk C-60. The C-60 cages in nanosheets can persist at pressures over 30 GPa, 3 GPa higher than for bulk C-60. These results suggest that C-60 crystals in even small size will be a potential candidate of superhard materials.
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| 3. |
- Chen, Ruikui, et al.
(författare)
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Photoinduced intramolecular charge-transfer state in thiophene-π-conjugated donor-acceptor molecules.
- 2008
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Ingår i: Journal of Molecular Structure. - : Elsevier BV. - 0022-2860 .- 1872-8014. ; 876:1-3, s. 102-109
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Tidskriftsartikel (refereegranskat)abstract
- Novel thiophene-π-conjugated donor-acceptor mols., 5-[2-(1,2,2,4-tetramethyl-1,2,3,4-tetrahydroquinolin-6-yl)-vinyl]-thiophene-2-carbaldehyde (QTC) and (1-cyano-2-{5-[2-(1,2,2,4-tetramethyl-1,2,3,4-tetrahydroquinolin-6-yl)-vinyl]-thiophen-2-yl}-vinyl)-phosphonic acid di-Et ester (QTCP), were designed and synthesized. Combined exptl. and theor. methods were performed to investigate the photoinduced intramol. charge-transfer (ICT) processes of these compds. Steady-state absorption and fluorescence measurements in different solvents indicate the photoinduced ICT characters of QTC and QTCP. Solvent dependency of the large Stokes shifts and high dipole moment of the excited state also support the charge-transfer character of the excited state. Theor. calcns. based on time-dependent d. functional theory (TDDFT) method were performed to investigate ICT states of these compds. The results reveal that the excited states have adopted a distortion of the C=C double bond between the donor moiety and the thiophene-π-bridge. [on SciFinder(R)]
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| 4. |
- Hou, Yuanyuan, et al.
(författare)
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Comparative study of pressure-induced polymerization of C60 nanorods and single crystals
- 2007
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Ingår i: Journal of Physics Condensed Matter. - Bristol : Institute of Physics. - 0953-8984 .- 1361-648X. ; 19:42, s. 425207-
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Tidskriftsartikel (refereegranskat)abstract
- In this paper, we report a comparative study of pressure-induced polymerization in C60 nanorods and bulk single crystals, treated simultaneously under various pressures and temperatures in the same experiment. For both materials, orthorhombic, tetragonal and rhombohedral phases have been produced under high pressure and high temperature. The structures have been identified and compared between the two sample types by Raman and photoluminescence spectroscopy. There are differences between the Raman and photoluminescence spectra from the two types of materials for all polymeric phases, but especially for the tetragonal phase. From the comparison between nanorods and bulk samples, we tentatively assign photoluminescence peaks for various polymeric phases.
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| 5. |
- Hou, Yuanyuan, et al.
(författare)
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Photoluminescence properties of high-pressure-polymerized C60 nanorods in the orthorhombic and tetragonal phases.
- 2006
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Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 89:18, s. 181925-
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Tidskriftsartikel (refereegranskat)abstract
- C60nanorods in two polymeric phases have been synthesized under differenthigh pressure and high temperature conditions. Orthorhombic and tetragonal phaseshave been identified from Raman spectra. The rod shape canbe kept under quasihydrostatic pressure. The photoluminescence intensity of thepolymeric C60 nanorods has been greatly enhanced compared with thatof pristine C60 nanorods. The main fluorescence band shifted from730 nm in the unpolymeric phase to 748 nm and near infrared780 nm in the orthorhombic and tetragonal phases, respectively. The enhancedphotoluminescence with tunable frequency for different polymeric C60 nanorods suggestspotential applications in luminescent nanomaterials.
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| 6. |
- Hou, Yuanyuan, et al.
(författare)
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Pressure-induced polymerization of nano- and submicrometer C60 rods into a rhombohedral phase
- 2006
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Ingår i: Chemical Physics Letters. - : Elsevier BV. - 0009-2614. ; 423:1-3, s. 215-219
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Tidskriftsartikel (refereegranskat)abstract
- C-60 rods with nano- and submicrometer dimensions were polymerized at 4.5 GPa and 973 K. Raman spectroscopy showed that the material transformed into a rhombohedral polymeric structure under high pressure and high temperature (HPHT) conditions. The HPHT polymerized samples keep the original rod shape. The position dependence of photoluminescence (PL) spectra have been studied on the rhombohedral polymer C60 rods at room temperature. The intensity of the 1.74 eV peak from the rhombohedral phase varies systematically between the edge of and the middle of the rod. Our results indicate that the 1.74 eV peak originates from surface defects.
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| 7. |
- Liu, Bingbing, et al.
(författare)
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Effects of silver films with different nano-particle sizes on SERS of single-walled carbon nanotubes
- 2005
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Ingår i: Chemical Journal of the Chinese Universities. - 0251-0790. ; 26:10, s. 1930-1933
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Tidskriftsartikel (refereegranskat)abstract
- Surface-enhanced Raman scattering (SERS) spectra of single-walled carbon nanotubes (SWCNTs) on silver films with different nano-particle sizes from 20 to 100 nm deposited on quartz and glass substrates were studied systematically. The characteristic Raman spectral features of SWCNT G-band and D-band were analyzed. The two bands show a similar tendency with the change of nano-particle size of silver on quartz and glass substrates. The position and the intensity of the G-band are less sensitive to the films' silver particle sizes in the studied range, indicating that hexagonal carbon rings are stable and have a weak interaction with silver films. The shape of the D-band depends on the silver size. The smaller the silver particle size, the more the contribution of high frequency vibrations to the D-band, indicating that disorder carbon has a strong interaction with the active silver films.
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| 8. |
- Liu, Bingbing, et al.
(författare)
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High pressure and high temperature induced polymeric C60 nanocrystal
- 2008
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Ingår i: Diamond and related materials, vol. 17, issue 4-5. - Amsterdam : Elsevier B.V.. ; , s. 620-623
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Konferensbidrag (refereegranskat)abstract
- In this paper, C60 nanosheets with polymeric phases have been obtained under various high pressures and high temperatures, including orthorhombic and tetragonal polymeric phases. The structures have been identified and compared with those of nanorods by photoluminescence and Raman spectroscopies. The main fluorescence band shifted from 1.70 eV in the monomeric phase to near infrared in the polymeric phase when pressure and temperature were increased. The difference of photoluminescence and Raman spectra between nanosheets and nanorods samples treated under the same conditions is probably caused by different polymerization degree in these samples because of different shapes.
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| 9. |
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| 10. |
- Wang, Lin, et al.
(författare)
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Highly Enhanced Luminescence from Single-Crystalline C60·1m-xylene Nanorods
- 2006
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Ingår i: Chemistry of Materials. - : American Chemical Society (ACS). - 0897-4756 .- 1520-5002. ; 18:17, s. 4190-4194
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Tidskriftsartikel (refereegranskat)abstract
- Single-crystalline C60â1m-xylene nanorods with a hexagonal structure were successfully synthesizedby evaporating a C60 solution in m-xylene at room temperature. The ratio of the length to the diameterof the nanorods can be controlled in the range of 10 to over 1000 for different applications. Thephotoluminescence (PL) intensity of the nanorods is about 2 orders of magnitude higher than that forpristine C60 crystals in air. Both UV and Raman results indicate that there is no charge transfer betweenC60 and m-xylene. It was found that the interaction between C60 and m-xylene molecules is of the vander Waals type. This interaction reduces the icosahedral symmetry of C60 molecule and induces strongPL from the solvate nanorods.
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