| Literature DB >> 28665670 |
Xigui Yang1, Mingguang Yao1, Xiangying Wu1, Shijie Liu1, Shuanglong Chen1, Ke Yang2, Ran Liu1, Tian Cui1, Bertil Sundqvist1,3, Bingbing Liu1.
Abstract
Design and synthesis of new carbon allotropes have always been important topics in condensed matter physics and materials science. Here we report a new carbon allotrope, formed from cold-compressed C_{70} peapods, which most likely can be identified with a fully sp^{3}-bonded monoclinic structure, here named V carbon, predicted from our simulation. The simulated x-ray diffraction pattern, near K-edge spectroscopy, and phonon spectrum agree well with our experimental data. Theoretical calculations reveal that V carbon has a Vickers hardness of 90 GPa and a bulk modulus ∼400 GPa, which well explains the "ring crack" left on the diamond anvils by the transformed phase in our experiments. The V carbon is thermodynamically stable over a wide pressure range up to 100 GPa, suggesting that once V carbon forms, it is stable and can be recovered to ambient conditions. A transition pathway from peapod to V carbon has also been suggested. These findings suggest a new strategy for creating new sp^{3}-hybridized carbon structures by using fullerene@nanotubes carbon precursor containing odd-numbered rings in the structures.Entities:
Year: 2017 PMID: 28665670 DOI: 10.1103/PhysRevLett.118.245701
Source DB: PubMed Journal: Phys Rev Lett ISSN: 0031-9007 Impact factor: 9.161