2010
DOI: 10.1021/nn101671t
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Soluble P3HT-Grafted Graphene for Efficient Bilayer−Heterojunction Photovoltaic Devices

Abstract: CH(2)OH-terminated regioregular poly(3-hexylthiophene) (P3HT) was chemically grafted onto carboxylic groups of graphene oxide (GO) via esterification reaction. The resultant P3HT-grafted GO sheets (G-P3HT) are soluble in common organic solvents, facilitating the structure/property characterization and the device fabrication by solution processing. The covalent linkage and the strong electronic interaction between the P3HT and graphene moieties in G-P3HT were confirmed by spectroscopic analyses and electrochemi… Show more

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Cited by 451 publications
(313 citation statements)
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“…In cases of covalent modifications, polymer chains are stably grafted to graphene sheets and surround them to prevent their aggregation caused by p-stacking. Two main approaches have been developed to covalently modify graphene materials with polymers: ''graft to'' 85 and ''graft from.'' 82 ''Graft to'' is chemically connecting polymer chains to the surfaces of CCG or GO sheets.…”
Section: Covalent Modificationmentioning
confidence: 99%
See 1 more Smart Citation
“…In cases of covalent modifications, polymer chains are stably grafted to graphene sheets and surround them to prevent their aggregation caused by p-stacking. Two main approaches have been developed to covalently modify graphene materials with polymers: ''graft to'' 85 and ''graft from.'' 82 ''Graft to'' is chemically connecting polymer chains to the surfaces of CCG or GO sheets.…”
Section: Covalent Modificationmentioning
confidence: 99%
“…In this case, the functional groups of polymer chains react with those of graphene sheets to form chemical connects. For example, the carboxylic groups of GO can react with hydroxyl or amine groups of a polymer via esterification 85 or amidation reactions 86,87 to form graphene/polymer composites.…”
Section: Covalent Modificationmentioning
confidence: 99%
“…Covalently connected P3HT ÀGO was also used in device active layers in attempts to facilitate electronic communication between the two materials. 125 P3HT-functionalized GO prepared by the reaction of hydroxylterminated P3HT with acid chloride functionalized GO revealed faster fluorescence decay of the P3HT exciton (380 ps) compared with simple blends of the two materials (476 ps), as determined by time-resolved photoluminescence spectroscopy. Moreover, cyclic voltammetry showed a decrease in the P3HT HOMO level by 0.1 eV, and narrowing of the bandgap by 0.7 eV, upon covalent attachment to GO.…”
Section: Nanoscale Assembly T Emrick and E Pentzermentioning
confidence: 91%
“…Esterifi cation/amidation is applied to covalently link the carboxylic groups on GO with the polymers containing hydroxyl or amine groups such as polyethylene glcol (PEG), 42 poly(vinyl alcohol) (PVA), 13,14 polyvinyl chloride, 43 poly(ethyleneimine), 44 triphenylamine-based polyazomethine 45 and poly(3-hexylthiophene). 46 Nitrene chemistry was reported to simply generate covalent linkage via cycloadditions of azide groups on the end of polymers (PEG, PS and polyacetylene) with C=C bonds in graphene. 25,47 Ring-opening reaction of epoxides is commonly used to form covalent bonding between epoxy and graphene prefunctionalized with amine groups.…”
Section: Functionalization Of Graphenementioning
confidence: 99%