| 1. |
- Nagel, Peter, et al.
(författare)
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C60 one- and two-dimensional polymers, dimers, and hard fullerite: Thermal expansion, anharmonicity, and kinetics of depolymerization
- 1999
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Ingår i: Physical Review B. Condensed Matter and Materials Physics. - : American Physical Society. - 1098-0121 .- 1550-235X. ; 60:24, s. 16920-16927
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Tidskriftsartikel (refereegranskat)abstract
- We report on high-resolution thermal expansion measurements of high-temperature-pressure treated C60 [one-dimensional (1D) and (2D) polymers and “hard fullerite”], as well as of C60 dimers and single crystal monomer C60 between 10 and 500 K. Polymerization drastically reduces the thermal expansivity from the values of monomeric C60 due to the stronger and less anharmonic covalent bonds between molecules. The expansivity of the “hard” material approaches that of diamond. The large and irreversible volume change upon depolymerization between 400 and 500 K makes it possible to study the kinetics of depolymerization, which is described excellently by a simple activated process, with activation energies of 1.9±0.1 eV (1D and 2D polymers) and 1.75±0.05 eV (dimer). Although the activation energies are very similar for the different polymers, the depolymerization rates differ by up to four orders of magnitude at a given temperature, being fastest for the dimers. Preliminary kinetic data of C70 polymers are presented as well.
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| 2. |
- Nagel, Peter, et al.
(författare)
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Intermolecular bond stability of C60 dimers and 2D pressure-polymerized C60
- 1998
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Ingår i: AIP Conference Proceedings Vol. 442. - Woodbury, NY : American Institute of Physics (AIP). - 1563968088 ; , s. 194-197
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Konferensbidrag (refereegranskat)abstract
- The thermal stability of C60 dimers and 2D pressure-polymerized C60 is studied using high-resolution capacitance dilatometry. The transformation of both the dimer and the polymer phases back to 'normal' C60 is excellently described by a simple thermally activated process with activation energies of 1.75 +/- 0.1 eV (dimer) and 1.9 +/- 0.2 eV (polymer). These results are compared to previous data for 1D-polymerized C60 and photo-polymerized C60. The thermal expansivity of the 2D-polymer phase is as much as a factor of ten smaller than that of pure C60 and approaches values for diamond.
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| 3. |
- Soldatov, Alexander, et al.
(författare)
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Polymeric fullerenes: from C60 to C70
- 1999
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Ingår i: AIP Conference Proceedings vol. 486. - Melville, NY : American Institute of Physics (AIP). - 1563969009 ; , s. 12-15
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Konferensbidrag (refereegranskat)abstract
- For the first time polymerization of both powder and single crystals of C70 fullerene was established after their subjection to high pressure (1.1 - 2 GPa) at elevated temperature (500 - 580 K). High-resolution capacitance dilatometry, FTIR/Raman spectroscopy and thermal conductivity were employed to characterise the polymeric phase of C70. The results demonstrate drastic changes in the physical properties of C70 on polymerization. We report on a reverse transformation to the monomeric state on heating the polymer to 500 K at ambient pressure. The activation energy of depolymerization was determined to be 1.8(1) eV. We discuss our results in terms of existing structural models for polymerization of C70 and compare the physical properties of C70 and C60 polymers.
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| 4. |
- Sundqvist, Bertil, et al.
(författare)
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Physical properties of two-dimensionally polymerized C60
- 1998
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Ingår i: Fullerenes: Recent Advances in the Chemistry and Physics of Fullerenes and Related Materials, vol. 6. - Pennington, NJ : The Electrochemical Society. - 1566772028 ; , s. 705-716
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Konferensbidrag (refereegranskat)abstract
- Preliminary data are reported for the thermal expansion, compressibility, and specific heat of two-dimensionally polymerized C60 obtained by treating fullerene samples at temperatures above 800 K under a pressure of 2 GPa. The samples have also been characterized by Raman spectroscopy and inelastic neutron scattering. The measured data for the thermophysical properties are strongly modified by the creation of strong covalent intermolecular bonds and we show that the results are compatible with the predictions of simple theories.
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