| Literature DB >> 28876939 |
Chuanxu Ma1, Liangbo Liang1, Zhongcan Xiao2, Alexander A Puretzky1, Kunlun Hong1, Wenchang Lu1,2, Vincent Meunier3, J Bernholc1,2, An-Ping Li1.
Abstract
Electrical contact to low-dimensional (low-D) materials is a key to their electronic applications. Traditional metal contacts to low-D semiconductors typically create gap states that can pin the Fermi level (EF). However, low-D metals possessing a limited density of states at EF can enable gate-tunable work functions and contact barriers. Moreover, a seamless contact with native bonds at the interface, without localized interfacial states, can serve as an optimal electrode. To realize such a seamless contact, one needs to develop atomically precise heterojunctions from the atom up. Here, we demonstrate an all-carbon staircase contact to ultranarrow armchair graphene nanoribbons (aGNRs). The coherent heterostructures of width-variable aGNRs, consisting of 7, 14, 21, and up to 56 carbon atoms across the width, are synthesized by a surface-assisted self-assembly process with a single molecular precursor. The aGNRs exhibit characteristic vibrational modes in Raman spectroscopy. A combined scanning tunneling microscopy and density functional theory study reveals the native covalent-bond nature and quasi-metallic contact characteristics of the interfaces. Our electronic measurements of such seamless GNR staircase constitute a promising first step toward making low resistance contacts.Entities:
Keywords: Electrical contact; graphene nanoribbon; heterostructure; scanning tunneling microscopy; staircase; vibrational modes
Year: 2017 PMID: 28876939 DOI: 10.1021/acs.nanolett.7b02938
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189