| Literature DB >> 29119629 |
Hyun-Tak Kim1, HyeonOh Shin1, In-Yup Jeon2,3, Masood Yousaf4, Jaeyoon Baik5, Hae-Won Cheong6, Noejung Park7, Jong-Beom Baek2, Tae-Hyuk Kwon1.
Abstract
The direct formation of CN and CO bonds from inert gases is essential for chemical/biological processes and energy storage systems. However, its application to carbon nanomaterials for improved energy storage remains technologically challenging. A simple and very fast method to form CN and CO bonds in reduced graphene oxide (RGO) and carbon nanotubes (CNTs) by an ultrasonic chemical reaction is described. Electrodes of nitrogen- or oxygen-doped RGO (N-RGO or O-RGO, respectively) are fabricated via the fixation between N2 or O2 carrier gas molecules and ultrasonically activated RGO. The materials exhibit much higher capacitance after doping (133, 284, and 74 F g-1 for O-RGO, N-RGO, and RGO, respectively). Furthermore, the doped 2D RGO and 1D CNT materials are prepared by layer-by-layer deposition using ultrasonic spray to form 3D porous electrodes. These electrodes demonstrate very high specific capacitances (62.8 mF cm-2 and 621 F g-1 at 10 mV s-1 for N-RGO/N-CNT at 1:1, v/v), high cycling stability, and structural flexibility.Entities:
Keywords: carbon nanomaterials; carbon-heteroatom bonds; energy storage systems; ultrasonic chemistry
Year: 2017 PMID: 29119629 DOI: 10.1002/adma.201702747
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849