Long-Range Ordered Carbon Clusters: A Crystalline Material with Amorphous Building Blocks
Author(s) -
Lin Wang,
Bingbing Liu,
Hui Li,
Wenge Yang,
Yang Ding,
Stanislav Sinogeikin,
Yue Meng,
Zhenxian Liu,
Xiao Cheng Zeng,
Wendy L. Mao
Publication year - 2012
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1220522
Subject(s) - amorphous solid , raman spectroscopy , materials science , translational symmetry , amorphous carbon , fullerene , carbon fibers , chemical physics , diamond , symmetry (geometry) , diffraction , crystallography , condensed matter physics , optics , chemistry , composite material , physics , organic chemistry , geometry , composite number , mathematics
Solid-state materials can be categorized by their structures into crystalline (having periodic translation symmetry), amorphous (no periodic and orientational symmetry), and quasi-crystalline (having orientational but not periodic translation symmetry) phases. Hybridization of crystalline and amorphous structures at the atomic level has not been experimentally observed. We report the discovery of a long-range ordered material constructed from units of amorphous carbon clusters that was synthesized by compressing solvated fullerenes. Using x-ray diffraction, Raman spectroscopy, and quantum molecular dynamics simulation, we observed that, although carbon-60 cages were crushed and became amorphous, the solvent molecules remained intact, playing a crucial role in maintaining the long-range periodicity. Once formed, the high-pressure phase is quenchable back to ambient conditions and is ultra-incompressible, with the ability to indent diamond.
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