Document Type
Article
Rights
Available under a Creative Commons Attribution Non-Commercial Share Alike 4.0 International Licence
Disciplines
1.3 PHYSICAL SCIENCES
Abstract
The effectiveness of polycyclic aromatic hydrocarbons (PAHs) for selective solubilisation of single walled carbon nanotubes (SWCNTs) has been studied by Raman spectroscopy. Polyphenyl and polyacene PAHs of different lengths are used. Selective interaction between the PAHs and SWCNT is investigated by analyzing the Raman radial breathing modes the frequency positioning of which yields information concerning the diameter distribution of the SWCNT sample. Samples were dispersed at concentrations below the debundling limit and deposited on quartz substrates. A combination of four laser excitation energies was utilized to establish the distribution of diameters present. The results show that the PAHs interact with a range of SWCNT diameters. In general a preference for smaller diameter SWCNTs is evident, although the longer PAHs have the capacity to solubilise larger diameter SWCNTs, due to their increased binding energy. Although a small degree of structural specificity is evident, all PAHs solubilise both chiral and nonchiral SWCNTs.
DOI
https://doi.org/10.1016/j.carbon.2009.12.044
Recommended Citation
Debnath, S. et al (2010) A Raman Spectroscopy Study of the Solubilisation of SWCNTS by Polycyclic Aromatic Hydrocarbons. Carbon, Vol.48, no. 5, pp.1489-1497. http://www.sciencedirect.com/science/journal/00086223. doi:10.1016/j.carbon.2009.12.044
Funder
Science Foundation Ireland
Publication Details
In Carbon, Vol.48, no.5, April, 2010 Available from http://www.sciencedirect.com/science/journal/00086223 This project is funded under the Science Foundation Ireland Research Frontiers Program PHY037 2006. The Raman Instrument was purchased under the framework of the INSPIRE programme, funded by the Irish Government’s Programme for Research in Third Level Institutions, Cycle 4, National Development Plan 2007–2013, supported by the European Union Structural Fund.