| 1. |
- 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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| 2. |
- 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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| 3. |
- 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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| 4. |
- Liu, Bingbing, et al.
(författare)
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High-pressure induced polymerization of C60 nanorods
- 2005
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Ingår i: Proceedings of the Joint 20th AIRAPT and 43rd EHPRG Conf. on High Pressure Science and Technology, Karlsruhe 2005. - 3923704496 ; , s. Nanomat-O133
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Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
- C60 nanorods, about 200 nm in diameter and several micrometers in length and with a rectangular cross section, have been synthesized by a simple solution-growth method. Raman spectroscopy and TEM indicate that the C60 nanorods have a fcc crystalline structure similar to that of pristine C60. Nanorods were polymerized at high temperature and high pressure below 2 GPa. Two different polymeric structures, orthorhombic and tetragonal as determined by Raman spectroscopy, have been obtained under different high temperature and high pressure conditions. The high-pressure induced polymeric samples keep the original nanometer scale rod shape.
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| 5. |
- Sundqvist, Bertil, et al.
(författare)
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Electrical transport properties of A4C60 (A=Li,Na,Rb) under pressure
- 2008
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Ingår i: High Pressure Research vol. 28 issue 4 December 2008. - London : Taylor & Francis. ; , s. 597-600
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Konferensbidrag (refereegranskat)abstract
- In search of structural phase transformations, the electrical resistances of the alkali metal-intercalated fullerene compounds Li4C60, Na4C60, and Rb4C60 have been measured as functions of temperature and pressure. The compounds have different lattice structures, and in the first two, the fullerene molecules form two-dimensional covalently bonded polymer lattices. No phase changes could be identified over the ranges 100-400 K and 0-2 GPa. All materials are semiconducting under the conditions studied, and we see no strong dependence of the band gaps on pressure.
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| 6. |
- Wang, Lin, et al.
(författare)
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High-pressure studies of Nano/sub-micrometer C70 rods
- 2005
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Ingår i: High Energy Physics and Nuclear Physics B. - 0254-3052. ; 29:Supplement, s. 112-115
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Tidskriftsartikel (refereegranskat)abstract
- We have successfully synthesized C-70 rods in nano/sub-micrometers scale by evaporating solvent method. The diameter of the as grown C-70 rods is similar to 500 nm, and the length is similar to 10 mu m. The EDXD pattern and Raman spectroscopy for as -grown sample indicate that the as grown C-70 rod is in hcp structure. The pressure-induced structural phase transition has been studied by using DAC combined with EDXD and Raman spectroscopy methods under quasi-hydrostatic pressure up to 26.1GPa. It is found that hcp structure transforms into amorphous phase for C-70 rods in the pressure range from 23.3 to 26.1GPa, which is higher than the transformation pressure for bulk C-70 crystals. The phase transition is irreversible and it is induced by the collapse of C-70 cage.
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| 7. |
- 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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| 8. |
- 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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| 9. |
- Wang, Lin, et al.
(författare)
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Synthesis of thin, rectangular C60 nanorods using m-xylene as shape controller
- 2006
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Ingår i: Advanced Materials. - : Wiley Interscience. - 0935-9648 .- 1521-4095. ; 18:14, s. 1883-1888
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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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| 10. |
- Yao, Mingguang, et al.
(författare)
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Effect of rare-earth component of the RE/Ni catalyst on the formation and nanostructure of single-walled carbon nanotubes
- 2006
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Ingår i: Journal of Physical Chemistry B. - : American Chemical Society (ACS). - 1520-6106 .- 1520-5207. ; 110:31, s. 15284-15290
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Tidskriftsartikel (refereegranskat)abstract
- A systematic experimental study has been carried out on the efficiency of bimetallic catalysts based on Ni and the rare-earth elements Y, La, Ce, Nd, Gd, Tb, Dy, Ho, Er, and Lu ( group A) and Eu, Sm, Yb, and Tm ( group B) in the synthesis of single-walled carbon nanotubes (SWNTs). The two groups give quite different results when analyzed by a combination of SEM/TEM and Raman and UV-NIR spectroscopies. The elements in group A have an obvious catalytic effect and increase the yield of SWNTs dramatically, whereas those in group B are not efficient catalysts. The diameter distribution of the synthesized SWNTs was also affected by the rare-earth element used. For group A metals, there is a tendency that the fraction of small-diameter tubes decreases with decreasing ionic radius of the rare-earth element used. EDX and X-ray analyses indicate that group A metals deposit on the cathode deposits and form rare-earth carbides, whereas no group B metals are found in cathode deposits, except for a small amount of Tm present in the form of thulium carbide. Further analysis indicates that there is a very strong correlation between the ability to form rare-earth carbides and the catalytic efficiency for the formation of SWNTs.
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