Journal
NATURE NANOTECHNOLOGY
Volume 10, Issue 3, Pages 248-252Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/NNANO.2015.1
Keywords
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Funding
- Fund for Scientific Research - Flanders (FWO) [G040011N, G021112N, 1513513N, G.0129.07, G.0206.12, 1523913N, G.0522.13N]
- UA-NOI-BOF grant
- Hercules Foundation
- EU ITN Nano2Fun
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Asymmetric dye molecules have unusual optical and electronic properties(1-3). For instance, they show a strong second-order nonlinear optical (NLO) response that has attracted great interest for potential applications in electro-optic modulators for optical telecommunications and in wavelength conversion of lasers(2,3). However, the strong Coulombic interaction between the large dipole moments of these molecules favours a pairwise antiparallel alignment that cancels out the NLO response when incorporated into bulk materials. Here, we show that by including an elongated dipolar dye (p,p'-dimethylaminonitrostilbene, DANS, a prototypical asymmetric dye with a strong NLO response(4)) inside single-walled carbon nanotubes (SWCNTs)(5,6), an ideal head-to-tail alignment in which all electric dipoles point in the same sense is naturally created. We have applied this concept to synthesize solution-processible DANS-filled SWCNTs that show an extremely large total dipole moment and static hyperpolarizability (beta(o) = 9,800 x 10(-30) e.s.u.), resulting from the coherent alignment of arrays of similar to 70 DANS molecules.
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