| 1. |
- Cui, Wen, et al.
(författare)
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High pressure and high temperature induced polymerization of doped C60 materials
- 2016
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Ingår i: Carbon. - : Elsevier. - 0008-6223 .- 1873-3891. ; 109, s. 269-275
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Tidskriftsartikel (refereegranskat)abstract
- Several metastable doped C60 polymers are synthesized under high pressure and high temperature (1.5GPa, 573K and 2GPa, 700K, respectively), using C60/ferrocene (Fc, Fe(C5H5)2), C60/Ni(OEP) and C60/AgNO3 as starting materials. Raman and IR spectroscopy are used to study the polymerization of these samples after HPHT treatment. It is found that the polymerization degree is always lower than that of pure C60 treated at same conditions, which is attributed to the space limitation by the dopants. We also find that even at same conditions, the three doped materials form different polymeric phases of the doped materials. This is attributed to the unique initial lattice structures and the different degrees of spatial confinement provided by the dopants.
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| 2. |
- Cui, Wen, et al.
(författare)
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Pressure induced metastable polymerization in doped C60 materials
- 2017
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Ingår i: Carbon. - : Elsevier. - 0008-6223 .- 1873-3891. ; 115, s. 740-745
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Tidskriftsartikel (refereegranskat)abstract
- High pressure Raman studies have been carried out on C60/AgNO3 and C60/Ni(OEP) up to 30 GPa. In both these doped C60 materials, pressure-induced metastable ordered polymers can be observed after pressure release. The results show that both the quenched materials contain chainlike polymers and dimers. We also find that the degree of polymerization is higher in these doped C60 materials than in bulk C60 materials after similar high pressure treatment and that C60/AgNO3 contains a higher fraction of chainlike polymers than C60/Ni(OEP) after decompression from same pressure. The results can be understood by considering the different initial lattice structures of these materials and the confinement effects of the dopants.
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| 3. |
- Cui, Wen, et al.
(författare)
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Reversible pressure-induced polymerization of Fe(C5H5)(2) doped C-70
- 2013
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Ingår i: Carbon. - : Pergamon-Elsevier Science. - 0008-6223 .- 1873-3891. ; 62, s. 447-454
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Tidskriftsartikel (refereegranskat)abstract
- High pressure Raman, IR and X-ray diffraction (XRD) studies have been carried out on C-70(Fe(C5H5)(2))(2) (hereafter, "C-70(Fc)(2)") sheets. Theoretical calculation is further used to analyze the Electron Localization Function (ELF) and charge transfer in the crystal and thus to understand the transformation of C-70(Fc)(2) under pressure. Our results show that even at room temperature dimeric phase and one dimensional (1D) polymer phase of C-70 molecules can be formed at about 3 and 8 GPa, respectively. The polymerization is found to be reversible Upon decompression and the reversibility is related to the pressure-tuned charge transfer, as well as the overridden steric repulsion of counter ions. According to the layered structure of the intercalated ferrocene molecules formed in the crystal, we suggest that ferrocene acts as not only a spacer to restrict the polymerization of C-70 molecules within a layer, but also as charge reservoir to tune the polymerization process. This supplies a possible way for us to design the polymerization of fullerenes at suitable conditions.
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| 4. |
- Cui, Wen, et al.
(författare)
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Synthesis of alkali-metal-doped C60 nanotubes
- 2011
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Ingår i: Diamond and Related Materials. - : Elsevier BV. ; , s. 93-96
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Konferensbidrag (refereegranskat)abstract
- C60 nanotubes have been synthesized by a solution–solution method. After degassing in a dynamic vacuum, the C60 nanotubes were doped with alkali metals by means of vapor evaporation method. Different temperatures have been studied to evaporate the alkali metals for the doping experiments. Raman spectrum was further employed to analyze the doping concentration of the obtained samples. It was found that all three alkali metals (Li, Na and K) used can be efficiently doped into the C60 nanotubes, forming AxC60 nanotubes. The doping concentration of Li, Na changed from low to high level, depending on the experiment temperatures, while K doping always gave saturated doping. The melt points, the ionic sizes and vapor pressures of alkali metals were thought to affect the final doping results.
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| 5. |
- Liu, Dedi, et al.
(författare)
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Effects of alcohols on shape-tuning and luminescence-enhancing of C70 nanocrystals
- 2013
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Ingår i: Optical materials (Amsterdam). - : Elsevier. - 0925-3467 .- 1873-1252. ; 36:2, s. 449-454
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Tidskriftsartikel (refereegranskat)abstract
- C70 nanotubes, nanorods and nanoparticles were produced by introducing a series of alcohols as precipitant into a C70/m-xylene solution. The effects of alcohols with different carbon chain lengths on the shape control of C70 nanocrystals were investigated. Alcohols with more than two carbon atoms in the longest chain linked to the hydroxyl groups induced the formation of C70 nanotube/rods. In contrast, alcohols containing two or fewer carbon atoms resulted in C70 nanoparticles. Structural analysis indicated that alcohol molecules exist in the C70 nanocrystals, forming solvated structures. The freshly formed C70 nanotubes and nanoparticles have orthorhombic and hexagonal solvated structures, respectively. Room temperature photoluminescence was further carried out on the solvated C70 nanocrystals to investigate their optical properties. We found that the luminescence intensities of C70 nanocrystals were significantly enhanced by the introduction of alcohols.
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| 6. |
- Liu, Dedi, et al.
(författare)
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High pressure and high temperature induced polymerization of C60 nanotubes
- 2011
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Ingår i: CrystEngComm. - : Royal Society of Chemistry. - 1466-8033. ; 13:10, s. 3600-3605
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Tidskriftsartikel (refereegranskat)abstract
- C60 nanotubes with outer diameters ranging from 400–800 nm were polymerized at 1.5 GPa, 573 K and 2.0 GPa, 700 K, respectively. Raman and photoluminescence spectroscopy were employed to characterize the polymeric phases of the treated samples. Both Raman and photoluminescence spectra showed that the C60 nanotubes transformed into the dimer and orthorhombic phases under the two different conditions, respectively. The photoluminescence peaks were tuned from visible to near infrared range. Comparative studies indicated that C60 nanotubes were more difficult to polymerize than bulk C60 material under the same conditions due to the nanoscale size effect in the C60 nanotubes.
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| 7. |
- Liu, Dedi, et al.
(författare)
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In situ Raman and photoluminescence study on pressure-induced phase transition in C60 nanotubes
- 2012
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Ingår i: Journal of Raman Spectroscopy. - : Wiley. - 0377-0486 .- 1097-4555. ; 43:6, s. 737-740
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Tidskriftsartikel (refereegranskat)abstract
- Single crystalline C60 nanotubes having face-centered-cubic structure with diameters in the nanometer range were synthesized by a solution method. In situ Raman and photoluminescence spectroscopy under high pressure were employed to study the structural stabilities and transitions of the pristine C60 nanotubes. A phase transition, probably because of the orientational ordering of C60 molecules, from face-centered-cubic structure to simple cubic structure occurred at the pressure between 1.46 and 2.26 GPa. At above 20.41 GPa, the Raman spectrum became very diffuse and lost its fine structure in all wavenumber regions, and only two broad and asymmetry peaks initially centered at 1469 and 1570cm-1 were observed, indicating an occurrence of amorphization. This amorphous phase remained to be reversible until 31.1 GPa, and it became irreversible to the ambient pressure after the pressure cycle of 34.3 GPa was applied.
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| 8. |
- Liu, Dedi, et al.
(författare)
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Pressure-induced phase transitions of C70 nanotubes
- 2011
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Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society. - 1932-7447 .- 1932-7455. ; 115:18, s. 8918-8922
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Tidskriftsartikel (refereegranskat)abstract
- Single crystalline C70 nanotubes having a face-centered-cubic (fcc) structure with diameters on a nanometer scale were synthesized by a facile solution method. In situ high pressure Raman spectroscopy and X-ray diffraction have been employed to study the structural stability and phase transitions of the pristine sample. We show that the molecular orientation-related phase transition from the fcc structure to a rhombohedral structure occurs at about 1.5 GPa, which is 1 GPa higher than in bulk C70. Also, the C70 molecules themselves are more stable in the nanotubes than in bulk crystals, manifested by a partial amorphization at 20 GPa. The crystal structure of C70 nanotubes could partially return to the initial structure after a pressure cycle above 30.8 GPa, and the C70 molecules were intact up to 43 GPa. The bulk modulus of C70 nanotubes is measured to be 50 GPa, which is twice larger than that of bulk C70.
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| 9. |
- Liu, Dedi, et al.
(författare)
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Synthesis and solid-state studies of self-assembled C60 microtubes
- 2011
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Ingår i: Diamond and Related Materials, vol. 20 issue 2. - : Elsevier BV. ; , s. 178-182
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Konferensbidrag (refereegranskat)abstract
- C60 microtubes were fabricated by a modified solution evaporation method, evaporating a solution of C60 in toluene in an atmosphere of m-xylene at room temperature. The C60 microtubes have outer diameters ranging from 2 to 8 μm. IR spectra, TG analysis and X-ray diffraction showed a solvated structure for the as-grown C60 microtubes. Through a gentle heat-treatment in vacuum, pure C60 microtubes with single crystalline fcc structure were obtained after the elimination of solvents. It is suggested that the C60 microtubes form through self-assembly from several individual C60 nanorods.
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| 10. |
- Yao, Mingguang, et al.
(författare)
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Pressure-induced transformation and superhard phase in fullerenes : the effect of solvent intercalation
- 2013
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Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 103:7, s. 071913-
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Tidskriftsartikel (refereegranskat)abstract
- We studied the behavior of solvated and desolvated C-60 crystals under pressure by in situ Raman spectroscopy. The pressure-induced bonding change and structural transformation of C60s are similar in the two samples, both undergoing deformation and amorphization. Nevertheless, the high pressure phases of solvated C-60 can indent diamond anvils while that of desolvated C(60)s cannot. Further experiments suggest that the solvents in the solvated C-60 act as both spacers and bridges by forming covalent bonds with neighbors in 3D network at high pressure, and thus, a fraction of fullerenes may preserve the periodic arrangement in spite of their amorphization.
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