Ambipolar Transport in Solution-Synthesized Graphene Nanoribbons

被引:48
作者
Gao, Jia [1 ]
Uribe-Romo, Fernando J. [2 ]
Saathoff, Jonathan D. [3 ]
Arslan, Hasan [2 ]
Crick, Colin R. [2 ]
Hein, Sam J. [2 ]
Itin, Boris [4 ]
Clancy, Paulette [3 ]
Dichtel, William R. [2 ]
Loo, Yueh-Lin [1 ]
机构
[1] Princeton Univ, Dept Chem & Biol Engn, Princeton, NJ 08544 USA
[2] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
[3] Cornell Univ, Baker Lab, Sch Chem & Biomol Engn, Ithaca, NY 14853 USA
[4] New York Struct Biol Ctr, 89 Convent Ave, New York, NY 10027 USA
基金
美国国家科学基金会;
关键词
solution-synthesized graphene nanoribbons; ambipolar transport; field-effect devices; aerosol-assisted chemical vapor deposition; inter-ribbon aggregation; CARBON; FIELD; BENZANNULATION; FABRICATION; TRANSISTORS; BEHAVIOR; FORM;
D O I
10.1021/acsnano.6b00643
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphene nanoribbons (GNRs) with robust electronic band gaps are promising candidate materials for nanometer-scale electronic circuits. Realizing their full potential, however, will depend on the ability to access GNRs with prescribed widths and edge structures and an understanding of their fundamental electronic properties. We report field-effect devices exhibiting ambipolar transport in accumulation mode composed of solution-synthesized GNRs with straight armchair edges. Temperature-dependent electrical measurements specify thermally activated charge transport, which we attribute to inter-ribbon hopping. With access to structurally precise materials in practical quantities and by overcoming processing difficulties in making electrical contacts to these materials, we have demonstrated critical steps toward nanoelectric devices based on solution-synthesized GNRs.
引用
收藏
页码:4847 / 4856
页数:10
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