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Träfflista för sökning "WFRF:(Yu Shidan) "

Sökning: WFRF:(Yu Shidan)

  • Resultat 1-10 av 13
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1.
  • Hou, Yuanyuan, et al. (författare)
  • Comparative study of pressure-induced polymerization of C60 nanorods and single crystals
  • 2007
  • Ingår i: Journal of Physics Condensed Matter. - Bristol : Institute of Physics. - 0953-8984 .- 1361-648X. ; 19:42, s. 425207-
  • 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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2.
  • Hou, Yuanyuan, et al. (författare)
  • Photoluminescence properties of high-pressure-polymerized C60 nanorods in the orthorhombic and tetragonal phases.
  • 2006
  • Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 89:18, s. 181925-
  • 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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3.
  • Hou, Yuanyuan, et al. (författare)
  • Pressure-induced polymerization of nano- and submicrometer C60 rods into a rhombohedral phase
  • 2006
  • Ingår i: Chemical Physics Letters. - : Elsevier BV. - 0009-2614. ; 423:1-3, s. 215-219
  • 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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4.
  • Liu, Bingbing, et al. (författare)
  • High pressure and high temperature induced polymeric C60 nanocrystal
  • 2008
  • Ingår i: Diamond and related materials, vol. 17, issue 4-5. - Amsterdam : Elsevier B.V.. ; , s. 620-623
  • 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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5.
  • Ma, Honglei, et al. (författare)
  • Synchrotron X-ray diffraction and infrared spectroscopy studies of C60H18 under high pressure
  • 2010
  • Ingår i: The Journal of Physical Chemistry Letters. - : American Chemical Society. - 1948-7185. ; 1:4, s. 714-719
  • Tidskriftsartikel (refereegranskat)abstract
    • In situ high-pressure angle-dispersive synchrotron X-ray diffraction and high-pressure mid-infrared (IR) spectrum measurements of C60H18 were carried out up to 32 and 10.2 GPa, respectively. Our diffraction data indicated that the fcc structure of C60H18 was stable up to 32 GPa. The bulk modulus B0 was determined to be 21 ± 1.16 GPa, about 40% higher than that of C60. The C−H vibrations still existed up to 10.2 GPa, and the vibrational frequencies decreased with increasing pressure. IR-active vibrational frequencies and their corresponding eigenvectors of C60H18 were simulated by DMOL3. The effects of the hydrogen atoms attached to the fullerene molecular cage on the stability of the structure under high pressure are discussed.
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6.
  • Wang, Lin, et al. (författare)
  • Highly Enhanced Luminescence from Single-Crystalline C60·1m-xylene Nanorods
  • 2006
  • Ingår i: Chemistry of Materials. - : American Chemical Society (ACS). - 0897-4756 .- 1520-5002. ; 18:17, s. 4190-4194
  • 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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7.
  • Wang, Lin, et al. (författare)
  • Synthesis and high pressure induced amorphization of C60 nanosheets
  • 2007
  • Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 91:10, s. 103112-
  • 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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8.
  • Wang, Lin, et al. (författare)
  • Synthesis of thin, rectangular C60 nanorods using m-xylene as shape controller
  • 2006
  • Ingår i: Advanced Materials. - : Wiley Interscience. - 0935-9648 .- 1521-4095. ; 18:14, s. 1883-1888
  • Tidskriftsartikel (refereegranskat)abstract
    • Thin, rectangular C60 nanorods in face-centered cubic structure are synthesized by using m-xylene as a shape controller. These unusual nanorods can easily grow on various substrates. The smallest nanorods have widths smaller than 30 nm. The nanorods are highly crystalline in single phase. A significant expansion of the lattice constant is also found in the C60 nanorods when their widths decrease below about 80 nm. 
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9.
  • Yao, Mingguang, et al. (författare)
  • Raman signature to identify the structural transition of single-wall carbon nanotubes under high pressure
  • 2008
  • Ingår i: Physical Review B. Condensed Matter and Materials Physics. - : American Physical Society. - 1098-0121 .- 1550-235X. ; 78:20
  • Tidskriftsartikel (refereegranskat)abstract
    • Raman spectra of single-walled carbon nanotubes (SWNTs) with diameters of 0.6–1.3 nm have been studied under high pressure. A “plateau” in the pressure dependence of the G-band frequencies was observed in all experiments, both with and without pressure transmission medium. Near the onset of the G-band plateau, the corresponding radial breathing mode (RBM) lines become very weak. A strong broadening of the full width at half maximum of the RBMs just before the onset of the G-band plateau suggests that a structural transition starts in the SWNTs. Raman spectra from SWNTs released from different pressures also indicate that a significant structural transition occurs during the G-band plateau process. Simulations of the structural changes and the corresponding Raman modes of a nanotube under compression show a behavior similar to the experimental observations. Based on the experimental results and the theoretical simulation, a detailed model is suggested for the structural transition of SWNTs, corresponding to the experimentally obtained Raman results in the high-pressure domain.
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10.
  • Yao, Mingguang, et al. (författare)
  • Synthesis and characterization of SWCNTs with Ho/Ni as catalyst
  • 2006
  • Ingår i: New Carbon Materials. - 1007-8827. ; 21:1, s. 70-74
  • Tidskriftsartikel (refereegranskat)abstract
    • SWCNTs were synthesized with high yield by DC arc discharge using Ho/Ni as catalysts. The morphologies, diameter distribution and the content of SWCNTs in the products were characterized by SEM, Raman scattering and TGA. Results indicate that SWCNTs can be efficiently synthesized with Ho/Ni as catalysts. The volume content of SWCNTs in a "web-like" form is as high as 80% in the product. Furthermore, the diameter distribution of SWCNTs, estimated by analyzing the resonance Raman scattering using excitation wavelengths of 632 and 488nm, varies from 1.35 to 1.69nm with a dominant diameter of 1.5nm, which is different from that of the SWCNTs synthesized with Ce/Ni as catalyst, proving that the diameter distribution of SWCNTs is dependent on the properties of the metal catalysts.
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  • Resultat 1-10 av 13

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