Please use this identifier to cite or link to this item: https://libjncir.jncasr.ac.in/xmlui/handle/10572/83
Full metadata record
DC FieldValueLanguage
dc.contributor.authorVarghese, Neenu-
dc.contributor.authorGhosh, Anupama-
dc.contributor.authorVoggu, Rakesh-
dc.contributor.authorGhosh, Sandeep-
dc.contributor.authorRao, C N R-
dc.date.accessioned2011-04-01T05:56:20Z-
dc.date.available2011-04-01T05:56:20Z-
dc.date.issued2009-10-01-
dc.identifier1932-7447en_US
dc.identifier.citationJournal of Physical Chemistry C 113(39), 16855–16859 (2009)en_US
dc.identifier.urihttps://libjncir.jncasr.ac.in/xmlui/10572/83-
dc.descriptionRestricted Access.en_US
dc.description.abstractInteraction of electron donor and acceptor molecules with graphene samples prepared by different methods as well as with single-walled carbon nanotubes (SWNTs) has been investigated by isothermal titration calorimetry (ITC). The ITC interaction energies of the graphene samples and SWNTs with electron acceptor molecules are higher than those with electron donor molecules. Thus, tetracyancethylene (TCNE) shows the highest interaction energy with both graphene and SWNTs. The interaction energy with acceptor molecules varies with the electron affinity as well as with the charge-transfer transition energy for different aromatics. Metallic SWNTs interact reversibly with electron. acceptor molecules, resulting in the opening of a gap.en_US
dc.description.urihttp://dx.doi.org/10.1021/jp9075355en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2009 American Chemical Societyen_US
dc.subjectPolycyclic Aromatic Hydrocarbonsen_US
dc.subjectCharge-Transferen_US
dc.titleSelectivity in the Interaction of Electron Donor and Acceptor Molecules with Graphene and Single-Walled Carbon Nanotubesen_US
dc.typeArticleen_US
Appears in Collections:Research Papers (Prof. C.N.R. Rao)

Files in This Item:
File Description SizeFormat 
S No 9 2009 J Phys Chem C (Letter) 113 16855.pdf
  Restricted Access
268.37 kBAdobe PDFView/Open Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.