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Edges Bring New Dimension to Graphene Nanoribbons
被引:66
|作者:
Gunlycke, Daniel
[1
]
Li, Junwen
[2
]
Mintmire, John W.
[2
]
White, Carter T.
[1
]
机构:
[1] USN, Res Lab, Div Chem, Washington, DC 20375 USA
[2] Oklahoma State Univ, Dept Phys, Stillwater, OK 74078 USA
关键词:
Graphene nanoribbon;
band gap;
twist;
density functional theory;
Huckel;
tight binding;
CARBON NANOTUBES;
STATE;
D O I:
10.1021/nl102034c
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Chemistry at the edges of saturated graphene nanoribbons can cause ribbons to leave the plane and form three-dimensional helical structures. Calculations, based on density functional theory and enabled by adopting helical symmetry, show that F-terminated armchair ribbons are intrinsically twisted in helices, unlike flat H-terminated strips. Twisting ribbons of either termination couple the conduction and valence bands, resulting in band gap modulation. This electromechanical response could be exploited in switches and sensor applications.
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页码:3638 / 3642
页数:5
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