Abstract
We demonstrate that dispersing a small amount of CdSeS gradient quantum dots (QDs) in a nematic liquid crystal and geometrically confining the nanocomposite in a polymer network leads to their ordered linear assembly, as observed through electron microscopy. Such an orientational order not only enhances the base photoluminescence (PL), but brings in significant anisotropy in the emission magnitude, a feature barely seen for the system without the polymer network. A high frequency (∼kHz) AC field adds the attractive dimension of on-demand and spatially addressable PL modulation. Using a photoisomerizable azobenzene derivative and a carefully selected excitation wavelength, it is shown that an actinic-light driven modulation of PL is also possible, which is furtherenhanced by the presence of the polymer network.
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