2015
DOI: 10.1039/c4tc01350f
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On the trade-off between processability and opto-electronic properties of single wall carbon nanotube derivatives in thin film heterojunctions

Abstract: A flow functionalization route has been employed to derivatize single wall carbon nanotubes (SWCNTs) by thienylphenyl groups. The SWCNT derivatives in the most soluble fraction have been characterized by thermogravimetric analysis, DLS analysis, DFT calculations, and UV-vis-NIR, microRaman and IR spectroscopies to study the degree of functionalization, the concentration of SWCNTs in solution, the dimension of the aggregates in solutions, the density of defects, and the presence of the thienylphenyl groups. Thi… Show more

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Cited by 22 publications
(16 citation statements)
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References 57 publications
(71 reference statements)
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“…A functionalization degree (FD, defined as the fraction of CNS carbon atoms that are functionalized with respect to the total carbon atoms) of 5% for SWCNT‐PhOMe and 3.4% for RGO‐PhOMe has been estimated from thermogravimetric analysis as expected (i.e., see refs. and ). The calculations are reported in the Supporting Information, together with the corresponding thermograms in Figures S5 and S6 (Supporting Information).…”
Section: Resultsmentioning
confidence: 96%
See 1 more Smart Citation
“…A functionalization degree (FD, defined as the fraction of CNS carbon atoms that are functionalized with respect to the total carbon atoms) of 5% for SWCNT‐PhOMe and 3.4% for RGO‐PhOMe has been estimated from thermogravimetric analysis as expected (i.e., see refs. and ). The calculations are reported in the Supporting Information, together with the corresponding thermograms in Figures S5 and S6 (Supporting Information).…”
Section: Resultsmentioning
confidence: 96%
“…Data on Hipco SWCNTs are available from the producer and have also been reported in our previous work (see ref. ). Data on RGO powder are reported in the Supporting Information (Figures S2 and S3).…”
Section: Methodsmentioning
confidence: 97%
“…In an effort towards such a direction, our group has studied the preparation of photoactive heterojunction active layers based on blends of poly(3‐hexylthiophene) (P3HT) and derivatized SWCNTs, which contain 4‐(thien‐2‐yl)phenyl (PhTh) moieties on the external surface, to improve their interaction with the thiophene‐based polymer 51. For the functionalization of SWCNTs, a previously reported approach based on aryldiazonium chemistry was initially followed by using 4‐(thien‐2‐yl)aniline in a flask at 80 °C for 4 h to generate in situ the reactive species (Scheme ).…”
Section: Organic Functionalized Cnss In Functional Pncsmentioning
confidence: 99%
“… Functionalization of SWCNTs with PhTh moieties under batch conditions. The synthesis of the 4‐(thien‐2‐yl)aniline derivative is also reported (Boc = tert ‐butoxycarbonyl) 51…”
Section: Organic Functionalized Cnss In Functional Pncsmentioning
confidence: 99%
“…Unfortunately, this does not often occur due to the stronger tendency of pristine GBMs to self‐aggregate, as it happens for the majority of CNSs, compromising the homogeneity of their dispersion within a polymer matrix . In this regard, resorting to chemical functionalization of pristine CNSs can be useful when the process is sufficiently controllable to avoid an excessive disruption of the native electronic structure . In the past, we have applied a coupled covalent chemical functionalization/sedimentation‐based separation (SBS) strategy to obtain homogeneous dispersion of RGO in a P3HT matrix .…”
Section: Introductionmentioning
confidence: 99%