Quantum Dots in Graphene Nanoribbons

被引:101
作者
Wang, Shiyong [1 ]
Kharche, Neerav [2 ]
Girao, Eduardo Costa [3 ]
Feng, Xinliang [4 ]
Muellen, Klaus [5 ]
Meunier, Vincent [2 ]
Fasel, Roman [1 ,6 ]
Ruffieux, Pascal [1 ]
机构
[1] Empa, Swiss Fed Labs Mat Sci & Technol, Uberlandstr 129, CH-8600 Dubendorf, Switzerland
[2] Rensselaer Polytech Inst, Dept Phys Appl Phys & Astron, Troy, NY 12180 USA
[3] Univ Fed Piaui, Dept Fis, BR-64049550 Teresina, Piaui, Brazil
[4] Tech Univ Dresden, Dept Chem & Food Chem, Mommsenstr 4, D-01062 Dresden, Germany
[5] Max Planck Inst Polymer Res, Ackermannweg 10, D-55128 Mainz, Germany
[6] Univ Bern, Dept Chem & Biochem, Freiestr 3, CH-3012 Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
Graphene quantum dot; graphene nanoribbon; scanning tunneling spectroscopy; density functional theory; screening; ON-SURFACE SYNTHESIS; QUASI-PARTICLE; BAND-GAP; RESONANCES; MICROSCOPY;
D O I
10.1021/acs.nanolett.7b01244
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphene quantum dots (GQDs) hold great promise for applications in electronics, optoelectronics, and bioelectronics, but the fabrication of widely tunable GQDs has remained elusive. Here, we report the fabrication of atomically precise GQDs consisting of low-bandgap N = 14 armchair graphene nanoribbon (AGNR) segments that are achieved through edge fusion of N = 7 AGNRs. The so-formed intraribbon GQDs reveal deterministically defined, atomically sharp interfaces between wide and narrow AGNR segments and host a pair of low-lying interface states. Scanning tunneling microscopy/spectroscopy measurements complemented by extensive simulations reveal that their energy splitting depends exponentially on the length of the central narrow bandgap segment. This allows tuning of the fundamental gap of the GQDs over 1 order of magnitude within a few nanometers length range. These results are expected to pave the way for the development of widely tunable intraribbon GQD-based devices.
引用
收藏
页码:4277 / 4283
页数:7
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