A new type of two-dimensional carbon crystal prepared from 1,3,5-trihydroxybenzene

被引:103
作者
Du, Qi-Shi [1 ,2 ]
Tang, Pei-Duo [1 ]
Huang, Hua-Lin [1 ]
Du, Fang-Li [1 ]
Huang, Kai [1 ]
Xie, Neng-Zhong [1 ]
Long, Si-Yu [1 ]
Li, Yan-Ming [1 ]
Qiu, Jie-Shan [1 ,3 ]
Huang, Ri-Bo [1 ]
机构
[1] Guangxi Acad Sci, State key Lab Bioenergy Enzyme Technol, Natl Engn Res Ctr Nonfood Biorefinery, Nanning, Peoples R China
[2] Gordon Life Sci Inst, 53 South Cottage Rd, Belmont, MA 02478 USA
[3] Dalian Univ Technol, Inst Carbon Mat, 2 Linggong Rd, Dalian 116024, Liaoning, Peoples R China
基金
美国国家科学基金会;
关键词
SET MODEL CHEMISTRY; RAMAN-SPECTROSCOPY; BENZYNE CONVERSION; GRAPHENE; 1,2-SHIFT; GRAPHITE; ORBITALS;
D O I
10.1038/srep40796
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A new two-dimensional (2D) carbon crystal, different from graphene, has been prepared from 1,3,5-trihydroxybenzene, consisting of 4-carbon and 6-carbon rings in 1: 1 ratio, named 4-6 carbophene by authors, in which all carbon atoms possess sp(2) hybrid orbitals with some distortion, forming an extensive conjugated pi-bonding planar structure. The angles between the three s-bonds of the carbon sp(2) orbitals are roughly 120 degrees, 90 degrees, and 150 degrees. Each of the three non-adjacent sides of a 6C-ring is shared with a 4C-ring; and each of the two opposite sides of a 4C-ring is shared with a 6C-ring. Dodecagonal holes with a diameter of approximate 5.8 angstrom are regularly located throughout the 2D carbon crystal. Even though the bond energies in 4-6 carbophene are weaker than those in the graphene, the new planar crystal is quite stable in ambient conditions. The 4-6 carbophene can be synthetized from 1,3,5-trihydroxybenzene or other benzene derivatives through dehydration and polymerization reactions, and may possess several possible patterns that form a family of 2D carbon crystals. A possible side reaction involving 1,3,5-trihydroxybenzene is also discussed, which may produce a carbon-oxygen two dimensional crystal.
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页数:11
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