| Literature DB >> 27313207 |
Javeed Mahmood1, Eun Kwang Lee2, Minbok Jung3, Dongbin Shin4, Hyun-Jung Choi1, Jeong-Min Seo1, Sun-Min Jung1, Dongwook Kim4, Feng Li1, Myoung Soo Lah4, Noejung Park5, Hyung-Joon Shin6, Joon Hak Oh7, Jong-Beom Baek8.
Abstract
The formation of 2D polyaniline (PANI) has attracted considerable interest due to its expected electronic and optoelectronic properties. Although PANI was discovered over 150 y ago, obtaining an atomically well-defined 2D PANI framework has been a longstanding challenge. Here, we describe the synthesis of 2D PANI via the direct pyrolysis of hexaaminobenzene trihydrochloride single crystals in solid state. The 2D PANI consists of three phenyl rings sharing six nitrogen atoms, and its structural unit has the empirical formula of C3N. The topological and electronic structures of the 2D PANI were revealed by scanning tunneling microscopy and scanning tunneling spectroscopy combined with a first-principle density functional theory calculation. The electronic properties of pristine 2D PANI films (undoped) showed ambipolar behaviors with a Dirac point of -37 V and an average conductivity of 0.72 S/cm. After doping with hydrochloric acid, the conductivity jumped to 1.41 × 10(3) S/cm, which is the highest value for doped PANI reported to date. Although the structure of 2D PANI is analogous to graphene, it contains uniformly distributed nitrogen atoms for multifunctionality; hence, we anticipate that 2D PANI has strong potential, from wet chemistry to device applications, beyond linear PANI and other 2D materials.Entities:
Keywords: C3N; nitrogenated graphene; polyaniline; solid-state reaction; two-dimensional
Year: 2016 PMID: 27313207 PMCID: PMC4941436 DOI: 10.1073/pnas.1605318113
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205