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从分子前体制备的石墨烯纳米带的能带隙调谐。

Tuning the band gap of graphene nanoribbons synthesized from molecular precursors.

机构信息

Department of Physics, University of California at Berkeley, Berkeley, California 94720, USA.

出版信息

ACS Nano. 2013 Jul 23;7(7):6123-8. doi: 10.1021/nn401948e. Epub 2013 Jun 12.

Abstract

A prerequisite for future graphene nanoribbon (GNR) applications is the ability to fine-tune the electronic band gap of GNRs. Such control requires the development of fabrication tools capable of precisely controlling width and edge geometry of GNRs at the atomic scale. Here we report a technique for modifying GNR band gaps via covalent self-assembly of a new species of molecular precursors that yields n = 13 armchair GNRs, a wider GNR than those previously synthesized using bottom-up molecular techniques. Scanning tunneling microscopy and spectroscopy reveal that these n = 13 armchair GNRs have a band gap of 1.4 eV, 1.2 eV smaller than the gap determined previously for n = 7 armchair GNRs. Furthermore, we observe a localized electronic state near the end of n = 13 armchair GNRs that is associated with hydrogen-terminated sp(2)-hybridized carbon atoms at the zigzag termini.

摘要

未来石墨烯纳米带 (GNR) 应用的一个前提条件是能够精细调整 GNR 的电子带隙。这种控制需要开发能够在原子尺度上精确控制 GNR 宽度和边缘几何形状的制造工具。在这里,我们报告了一种通过新的分子前体的共价自组装来修饰 GNR 带隙的技术,该技术产生了 n = 13 的扶手椅型 GNR,这是比以前使用自下而上的分子技术合成的更宽的 GNR。扫描隧道显微镜和光谱学揭示,这些 n = 13 的扶手椅型 GNR 的带隙为 1.4 eV,比之前确定的 n = 7 的扶手椅型 GNR 的带隙小 1.2 eV。此外,我们在 n = 13 的扶手椅型 GNR 的末端附近观察到一个局域电子态,该态与锯齿状末端处氢化的 sp(2)杂化碳原子有关。

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