| Literature DB >> 27934214 |
Xu Zhang1, Yuan Huang1, Shanshan Chen2, Na Yeon Kim3, Wontaek Kim4, David Schilter1, Mandakini Biswal1, Baowen Li1, Zonghoon Lee1,3, Sunmin Ryu4,5, Christopher W Bielawski1,6,7, Wolfgang S Bacsa8, Rodney S Ruoff1,6,3.
Abstract
Few-layer graphenes, supported on Si with a superficial oxide layer, were subjected to a Birch-type reduction using Li and H2O as the electron and proton donors, respectively. The extent of hydrogenation for bilayer graphene was estimated at 1.6-24.1% according to Raman and X-ray photoelectron spectroscopic data. While single-layer graphene reacts uniformly, few-layer graphenes were hydrogenated inward from the edges and/or defects. The role of these reactive sites was reflected in the inertness of pristine few-layer graphenes whose edges were sealed. Hydrogenation of labeled bilayer (12C/13C) and trilayer (12C/13C/12C) graphenes afforded products whose sheets were hydrogenated to the same extent, implicating passage of reagents between the graphene layers and equal decoration of each graphene face. The reduction of few-layer graphenes introduces strain, allows tuning of optical transmission and fluorescence, and opens synthetic routes to long sought-after films containing sp3-hybridized carbon.Entities:
Year: 2016 PMID: 27934214 DOI: 10.1021/jacs.6b08625
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419