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• 1. [Article] Structure, Dynamics, and Phase Transitions in the Fullerene Derivatives C_{60}O and C_{61}H_{2}

  The effect of perturbing the icosohedral symmetry of C60 by the addition of the side groups -O and -CH2 upon orientational order-disorder and glass transitions in solid C60 has been studied by a combination ...

  Citation × Citation Citation Abstract Copy Title: Structure, Dynamics, and Phase Transitions in the Fullerene Derivatives C_{60}O and C_{61}H_{2} Author: Meingast, C., Roth, G., Pintschovius, L., Michel, R. H., Stoermer, C., Kappes, M. M., Heiney, Paul A., Brard, Laurent, Strongin, Robert M., Smith, Amos B., III Year: 1996 The effect of perturbing the icosohedral symmetry of C60 by the addition of the side groups -O and -CH2 upon orientational order-disorder and glass transitions in solid C60 has been studied by a combination of high-resolution capacitance dilatometry and single-crystal x-ray and powder inelastic neutron scattering. Both fullerene derivatives C60O (epoxide) and C61H2 (6,5-annulene) are shown to undergo a sequence of transitions similar to that found in pure C60, i.e., a first-order orientational ordering transition just below room temperature followed by an orientational glass transition at lower temperatures. Although the exact origin of the glass transition in C61H2 is unclear, the glass transition in C60O has the same origin as that in C60, with a significantly higher degree of order due to a larger energy difference between pentagon and hexagon orientations. The dilatometric data at the glass transition indicate that, in contrast to C60, the ground-state orientation of both C60O and C61H2 molecules is that with the smallest volume, also demonstrating a significant influence of the side groups upon the details of the structure. A possible explanation of these differences in terms of steric effects is proposed. Title: Structure, Dynamics, and Phase Transitions in the Fullerene Derivatives C_{60}O and C_{61}H_{2} Author: Meingast, C., Roth, G., Pintschovius, L., Michel, R. H., Stoermer, C., Kappes, M. M., Heiney, Paul A., Brard, Laurent, Strongin, Robert M., Smith, Amos B., III Year: 1996 The effect of perturbing the icosohedral symmetry of C60 by the addition of the side groups -O and -CH2 upon orientational order-disorder and glass transitions in solid C60 has been studied by a combination of high-resolution capacitance dilatometry and single-crystal x-ray and powder inelastic neutron scattering. Both fullerene derivatives C60O (epoxide) and C61H2 (6,5-annulene) are shown to undergo a sequence of transitions similar to that found in pure C60, i.e., a first-order orientational ordering transition just below room temperature followed by an orientational glass transition at lower temperatures. Although the exact origin of the glass transition in C61H2 is unclear, the glass transition in C60O has the same origin as that in C60, with a significantly higher degree of order due to a larger energy difference between pentagon and hexagon orientations. The dilatometric data at the glass transition indicate that, in contrast to C60, the ground-state orientation of both C60O and C61H2 molecules is that with the smallest volume, also demonstrating a significant influence of the side groups upon the details of the structure. A possible explanation of these differences in terms of steric effects is proposed. Close

• 2. [Article] Structure and Phase Transition of the 6,5-Annulene Isomer of C_{61}H_{2}

  We have used differential scanning calorimetry and x-ray diffraction to study the crystalline phases of the 6,5-annulene isomer of C61H2. At 308 K the methylenated fullerenes are orientationally disordered ...

  Citation × Citation Citation Abstract Copy Title: Structure and Phase Transition of the 6,5-Annulene Isomer of C_{61}H_{2} Author: Lommen, Andrea N., Heiney, Paul A., Vaughan, Gavin B. M., Stephens, Peter W., Liu, Dengfa, Li, Dayin, Smith, Allan L., McGhie, Andrew R., Strongin, Robert M., Brard, Laurent, Smith, Amos B., III Year: 1994 We have used differential scanning calorimetry and x-ray diffraction to study the crystalline phases of the 6,5-annulene isomer of C61H2. At 308 K the methylenated fullerenes are orientationally disordered in a face-centered cubic lattice with lattice parameter 14.19±0.02 Å. Below Tc=290 K the symmetry is lowered to Pa3¯, a simple-cubic structure. At 20 K the lattice parameter is 14.06±0.02 Å, with substantial statistical disorder remaining. The transition temperature in C61H2 is slightly higher than in C60O and higher still than in C60, but the three compounds exhibit orientationally ordering transitions between qualitatively similar phases. Title: Structure and Phase Transition of the 6,5-Annulene Isomer of C_{61}H_{2} Author: Lommen, Andrea N., Heiney, Paul A., Vaughan, Gavin B. M., Stephens, Peter W., Liu, Dengfa, Li, Dayin, Smith, Allan L., McGhie, Andrew R., Strongin, Robert M., Brard, Laurent, Smith, Amos B., III Year: 1994 We have used differential scanning calorimetry and x-ray diffraction to study the crystalline phases of the 6,5-annulene isomer of C61H2. At 308 K the methylenated fullerenes are orientationally disordered in a face-centered cubic lattice with lattice parameter 14.19±0.02 Å. Below Tc=290 K the symmetry is lowered to Pa3¯, a simple-cubic structure. At 20 K the lattice parameter is 14.06±0.02 Å, with substantial statistical disorder remaining. The transition temperature in C61H2 is slightly higher than in C60O and higher still than in C60, but the three compounds exhibit orientationally ordering transitions between qualitatively similar phases. Close

• 3. [Article] Coherence Peak and Superconducting Energy Gap in Rb_{3}C_{60} Observed by Muon Spin Relaxation

  Muon spin relaxation resulting from spin exchange scattering of endohedral muonium (μ+e-) with thermal electronic excitations has been observed in the fullerene superconductor Rb3C60. The temperature dependence ...

  Citation × Citation Citation Abstract Copy Title: Coherence Peak and Superconducting Energy Gap in Rb_{3}C_{60} Observed by Muon Spin Relaxation Author: Kiefl, R. F., MacFarlane, W. A., Chow, K. H., Dunsiger, S., Duty, T. L., Johnston, T. M. S., Schneider, J. W., Sonier, J., Brard, Laurent, Strongin, Robert M., Fischer, J. E., Smith, Amos B., III Year: 1993 Muon spin relaxation resulting from spin exchange scattering of endohedral muonium (μ+e-) with thermal electronic excitations has been observed in the fullerene superconductor Rb3C60. The temperature dependence of T1-1 shows a coherence peak just below Tc and can be fit to the conventional Hebel-Slichter theory for spin relaxation in a superconductor with a broadened BCS density of states. The average energy gap for electronic excitations, Δ/kB=53(4) K or 2Δ/ kBTc=3.6(3), is consistent with the BCS weak coupling limit. Title: Coherence Peak and Superconducting Energy Gap in Rb_{3}C_{60} Observed by Muon Spin Relaxation Author: Kiefl, R. F., MacFarlane, W. A., Chow, K. H., Dunsiger, S., Duty, T. L., Johnston, T. M. S., Schneider, J. W., Sonier, J., Brard, Laurent, Strongin, Robert M., Fischer, J. E., Smith, Amos B., III Year: 1993 Muon spin relaxation resulting from spin exchange scattering of endohedral muonium (μ+e-) with thermal electronic excitations has been observed in the fullerene superconductor Rb3C60. The temperature dependence of T1-1 shows a coherence peak just below Tc and can be fit to the conventional Hebel-Slichter theory for spin relaxation in a superconductor with a broadened BCS density of states. The average energy gap for electronic excitations, Δ/kB=53(4) K or 2Δ/ kBTc=3.6(3), is consistent with the BCS weak coupling limit. Close