Search

Blinking of zinc blende CdSe-based core/shell nanocrystals is studied as a function of shell materials and surface ligands. CdSe/ZnS, CdSe/ZnSe/ZnS and CdSe/CdS/ZnS core/shell nanocrystals are prepared by colloidal synthesis and six monolayers of larger bandgap shell materials are grown over the CdSe core. Organic-soluble nanocrystals covered with stearate are made water-soluble by ligand exchange with 3-mercaptopropionic acid. The light-emitting states of nanocrystals are characterized by absorption and emission spectroscopy as well as photoluminescence lifetime measurements in solution. The blinking time trace is recorded for single nanocrystals on a glass coverslip. Both on- and off-time distributions are fitted to the power law. The power-law exponents vary, depending on shell materials and surface ligands. The off-time exponents for organic and water-soluble nanocrystals are measured in the range of 1.36-1.55 and 1.25-1.37, respectively, while their on-time exponents are spread in the range of 1.53-1.86 and 1.85-2.17, respectively. Water-soluble surface passivation with thiolate prolongs the dark period regardless of shell materials and core/shell structures. Of the core/shell structures, CdSe/CdS/ZnS exhibits the longest bright state. The on/off-time exponents are inversely correlated, although the successive on/off events are not individually correlated. A two competing charge-tunneling model is presented to describe the variation of on- and off-time exponents with shell materials and surface ligands.

We present a simple method for size determination of nanoparticles using conventional optical microscopes. The method, called through-focus scanning optical microscopy, makes use of the four-dimensional optical information collected at different focus positions. Low partial coherence illumination combined with analysis of through-focus optical content enables nanoparticle size determination with nanometer scale sensitivity. We experimentally demonstrate this using fabricated Si nanodots and spherical gold nanoparticles. The method is economical, as no hardware modifications to conventional optical microscopes are needed. In addition, the method also has high throughput and potential for soft nanoparticle size determination without distortion. [ABSTRACT FROM AUTHOR]