2015
DOI: 10.1021/acs.jpcc.5b09049
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Self-Assembly and Visualization of Poly(3-hexyl-thiophene) Chain Alignment along Boron Nitride Nanotubes

Abstract: /npsi/ctrl?lang=en http://nparc.cisti-icist.nrc-cnrc.gc.ca/npsi/ctrl?lang=fr READ THESE TERMS AND CONDITIONS CAREFULLY BEFORE USING THIS WEBSITE.http://nparc.cisti-icist.nrc-cnrc.gc.ca/npsi/jsp/nparc_cp.jsp?lang=en Vous avez des questions? Nous pouvons vous aider. Pour communiquer directement avec un auteur, consultez la première page de la revue dans laquelle son article a été publié afin de trouver ses coordonnées. Si vous n'arrivez pas à les repérer, communiquez avec nous à PublicationsArchive-ArchivesPubli… Show more

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Cited by 32 publications
(56 citation statements)
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“…to oxidize amorphous boron to B 2 O 3 27,37,[70][71][72] . The optimal oxidation temperature was chosen based on the TGA results in Figure 2e-g, and the exposure time was fixed to 6 h to remove amorphous boron.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…to oxidize amorphous boron to B 2 O 3 27,37,[70][71][72] . The optimal oxidation temperature was chosen based on the TGA results in Figure 2e-g, and the exposure time was fixed to 6 h to remove amorphous boron.…”
Section: Resultsmentioning
confidence: 99%
“…In particular, BNNT has not only the unique 1D structure stable up to a temperature of 850 °C but also their superior mechanical properties and chemical resistance 7,9,10,19,[21][22][23] . Therefore, BNNTs among BN materials have been applied to various applications, such as BNNT-polymer composites, BNNT-metal composites, and biological applications 7,9,10,12,15,21,[24][25][26][27][28][29][30][31][32][33] . Additionally, since BNNTs have abundant B 10 isotope, which has the largest scattering cross-section for neutron absorption among low Z atoms, they can be employed as a neutron shielding agent 24,34,35 .…”
mentioning
confidence: 99%
“…Upon addition of BNNTs, the polymers aggregate with the BNNTs, similar to how poly(carbazole)s have been shown to aggregate with themselves [ 46 ] and poly(thiophene)s aggregate to the surface of BNNTs through strong π‐π interactions. [ 30 ] This aggregation is evident by a red‐shift of the maximum absorption and the presence of partially resolved band structure for all four polymers (Figure 4). The red‐shift for the homopolymers of 45 and 47 nm was significantly larger than for the heteropolymers (31 and 20 nm, Table 2).…”
Section: Resultsmentioning
confidence: 97%
“…Noncovalent functionalization of BNNTs has been reported in the literature, with both conjugated polymers and small molecules exploiting the presence of π‐electrons in the BNNT backbone. [ 27 ] Poly[ m ‐phenylenevinylene‐ co ‐(2,5‐dioctoxy‐ p ‐phenylenevinylene)] (PmPV), [ 15,28 ] rigid‐rod poly( p ‐phenyleneethynylene) derivatives and poly(thiophene)s [ 29–31 ] have all been employed to disperse BNNTs into organic solvents, [ 29 ] whereas aqueous dispersions of BNNTs have been prepared with anionic perylene. [ 32 ] These examples suggest that BNNTs can be selectively coated by the conjugated polymers or small molecules, rendering them soluble and offering a route toward the removal of non‐nanotube impurities.…”
Section: Introductionmentioning
confidence: 99%
“…The asproduced BNNT material was purified by use of molecular chlorine at elevated temperature to etch various impurities as reported recently. [40] Details on the preparation of the dispersions and noncovalent functionalization with regiorandom poly(3-hexylthiophene-2,5-diyl) (rra-P3HT) can be found in the work completed by Martinez-Rubi et al [41] A 0.2 mg mL −1 suspension of rra-P3HT functionalized BNNTs in chloroform was spray-coated on Melinex using an Iwata Air Brush Studio Series Smart Jet air compressor to generate PET coated films containing BNNT surface concentrations of 36, 71, and 142 mg m −2 , respectively.…”
Section: Methodsmentioning
confidence: 99%