| Literature DB >> 27463961 |
Yinjuan Huang1, Yiyong Mai1, Uliana Beser2, Joan Teyssandier3, Gangamallaiah Velpula3, Hans van Gorp3, Lasse Arnt Straasø4, Michael Ryan Hansen5, Daniele Rizzo6, Cinzia Casiraghi6, Rong Yang7, Guangyu Zhang7, Dongqing Wu1, Fan Zhang1, Deyue Yan1, Steven De Feyter3, Klaus Müllen2, Xinliang Feng1,8.
Abstract
Structurally well-defined graphene nanoribbons (GNRs) have attracted great interest as next-generation semiconductor materials. The functionalization of GNRs with polymeric side chains, which can widely broaden GNR-related studies on physiochemical properties and potential applications, has remained unexplored. Here, we demonstrate the bottom-up solution synthesis of defect-free GNRs grafted with flexible poly(ethylene oxide) (PEO) chains. The GNR backbones possess an armchair edge structure with a width of 1.0-1.7 nm and mean lengths of 15-60 nm, enabling near-infrared absorption and a low bandgap of 1.3 eV. Remarkably, the PEO grafting renders the GNRs superb dispersibility in common organic solvents, with a record concentration of ∼1 mg mL(-1) (for GNR backbone) that is much higher than that (<0.01 mg mL(-1)) of reported GNRs. Moreover, the PEO-functionalized GNRs can be readily dispersed in water, accompanying with supramolecular helical nanowire formation. Scanning probe microscopy reveals raft-like self-assembled monolayers of uniform GNRs on graphite substrates. Thin-film-based field-effect transistors (FETs) of the GNRs exhibit a high carrier mobility of ∼0.3 cm(2) V(-1) s(-1), manifesting promising application of the polymer-functionalized GNRs in electronic devices.Entities:
Year: 2016 PMID: 27463961 DOI: 10.1021/jacs.6b07061
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419