ABSTRACT
The addition of octylamine-modified poly(acrylic acid) to nanocrystal quantum dots (NQDs) results in robust, alcohol-soluble nanoparticles that can be readily incorporated into titania matrices without large changes in photoluminescence quantum yields. This approach relies on the amphiphilic nature of the polymer to create an NQD-polymer complex in which the alkyl chains interact with the hydrophobic part of the NQD, leaving the polar carboxylic acid groups on the periphery. This procedure is applicable to hydrophobically capped NQDs of a variety of shapes and compositions, making it a truly generalized route to nanocrystal-titania nanocomposites.
Subject(s)
Nanotechnology/methods , Quantum Dots , Titanium/chemistry , Polymers/chemistryABSTRACT
Isolated europium-doped metal-oxide nanoparticles were probed by size-correlated high-numerical-aperture (far-field) imaging techniques. A modified Digital Instruments Bioscope atomic force microscope mounted upon a Nikon TE300 inverted microscope was used to interrogate (dry) particles ranging in size from 2 to 150 nm on the surface of a glass or quartz coverslip. These experiments revealed several interesting features of doped-nanoparticle luminescence such as Poissonian occupation statistics, size-dependent luminescence efficiency enhancement for particle sizes of <10 nm, and correlation of interesting transient behavior at particle sizes of <5 nm.
ABSTRACT
Measuring three-dimensional orientational motions of many individual molecules within glassy state poly(methyl methacrylate) has enabled nanoscopic probing of bulk-obscured polymer dynamics. Complementing bulk studies, the measured distributions of nanoscale barriers to rotational motion afforded by our single molecule orientational methods directly probe the spatial heterogeneity and nanoscopic alpha-relaxation dynamics deep within the glassy state.
