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Bond switching from two- to three-dimensional polymers ofC60at high pressure
Author(s) -
Dam Hieu,
Yoshihiro Iwasa,
T. Takano,
Tetsu Watanuki,
Yasuo Ohishi,
S. Yamanaka
Publication year - 2003
Publication title -
physical review. b, condensed matter
Language(s) - English
Resource type - Journals
eISSN - 1095-3795
pISSN - 0163-1829
DOI - 10.1103/physrevb.68.153402
Subject(s) - polymer , materials science , diamond , tetragonal crystal system , anisotropy , phase (matter) , crystallography , order (exchange) , diffraction , molecule , transformation (genetics) , physics , optics , chemistry , composite material , quantum mechanics , biochemistry , finance , economics , gene
In situ high pressure x-ray diffraction experiments revealed that a transformation from the two-dimensional (2D) tetragonal ${\mathrm{C}}_{60}$ polymer to a three-dimensional (3D) polymer takes place via a highly anisotropic deformation of ${\mathrm{C}}_{60}$ molecules along the c axis, as an irreversible first-order transformation above 20 GPa. In the 3D polymer phase, the $2+2$ bonds remain in the 2D plane, while neighboring layers are connected by the $3+3$ bonds. The bulk modulus of the 3D polymer was 407 GPa, being slightly smaller than that of diamond.

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