The liquid-liquid interfacial precipitation method was employed to prepare (C
60)
1−x(C
70)
x solids having good crystallinity. In reference to the case of pure C
60 (Y. Takahashi
et al.: J. Japan Inst. Metals
68(2004) 326), toluene and methyl alcohol were used as good and poor solvents, respectively. Under ambient pressure, the solids were successfully formed up to
x=0.09, but failed to form at
x≧0.10 because a (C
60)
1−x(C
70)
x•C
6H
5CH
3 solvate was included. However, under a high pressure argon atmosphere, formation of the solvate was highly suppressed and only (C
60)
1−x(C
70)
x solids were obtained for all
x when
P≧4 MPa. Electron probe microanalysis identified the presence of argon in the solid. Thus it is likely that incorporation of argon atoms in the solid during precipitation disturbs solvate formation. The argon atoms were removed by heat-treatment in a vacuum at 300℃, providing pure C
60-C
70 solids.
The specimens were measured by X-ray diffraction to clarify the miscibility gap between the C
60-rich phase and the C
70-rich phase. The former solubility limit was evaluated to be
x=0.09, while the latter was in the range of
x=0.8-0.9. From the
x-dependence of the lattice parameter in the C
60-rich phase, the partial molar volume of dissolved C
70 was estimated to be smaller than that of pure C
70 by only 2.6%. The system can be modeled by hard-contact mixing of two different spheres. A large tensile distortion exists in the C
60 matrix in the vicinity of a C
70 molecule along with an accompanying strain energy. This acts as the driving force of phase separation in the system.
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