Fluorescence blinking statistics from CdSe core and core/shell nanorods.
نویسندگان
چکیده
We report fluorescence blinking statistics measured from single CdSe nanorods (NRs) of seven different sizes with aspect ratios ranging from 3 to 11. This study also included core/shell CdSe/ZnSe NRs and core NRs with two different surface ligands producing different degrees of surface passivation. We compare the findings for NRs to our measurements of blinking statistics from spherical CdSe core and CdSe/ZnS core/shell nanocrystals (NCs). We find that, for both NRs and spherical NCs, the off-time probability distributions are well described by a power law, while the on-time probability distributions are best described by a truncated power law, P(tau(on)) approximately tau(on)(-alpha)e((-tau)(on)/(tau)(c)). The measured crossover time, tau(c), is indistinguishable within experimental uncertainty for core and core/shell NRs, as well as for core NRs with different ligands, for the same core size, indicating that surface passivation does not affect the blinking statistics significantly. We find that, at fixed excitation intensity, 1/tau(c) increases approximately linearly with increasing NR aspect ratio; for a given sample, 1/tau(c) increases very gradually with increasing excitation intensity. Examining 1/tau(c)versus the single-particle photon absorption rate for all samples indicates that the change in NR absorption cross section with sample size can account for some but not all of the differences in crossover time. This suggests that the degree of quantum confinement may be partially responsible for the aspect ratio dependence of the crossover time.
منابع مشابه
Shell and ligand-dependent blinking of CdSe-based core/shell nanocrystals.
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 excha...
متن کاملSingle dot luminescence characteristics of CdSe/ZnS core-shell structured quantum dots with different ligands
Chemical derivatizations with different ligands were perfomed on CdSe/ZnS core-shell quantum dots (QDs). The ligands serve a role to increase water solubility and bio-compatibility of QDs in the application of in vivo biomedical fluorescence imaging. These QDs were synthesized with various capping agents and optically characterized by using single molecule detection technique to investigate the...
متن کاملDirect observation of the radial breathing mode in CdSe nanorods.
We experimentally confirm the existence of the radial breathing mode in CdSe nanorods by Raman spectroscopy, which was deduced from ab initio calculations of the vibrational properties of bare CdSe nanowires and CdSe/ZnS core-shell nanowires. We calculated the modes' frequency for various diameters and measured a set of bare CdSe nanorods and CdSe/ZnS core-shell nanorods to determine the diamet...
متن کاملEpitaxial growth and photochemical annealing of graded CdS/ZnS shells on colloidal CdSe nanorods.
We report the preparation and structural characterization of core/shell CdSe/CdS/ZnS nanorods. A graded shell of larger band gap is grown around CdSe rods using trioctylphosphine oxide as a surfactant. Interfacial segregation is used to preferentially deposit CdS near the core, providing relaxation of the strain at the core/shell interface. The reported synthesis allows for variation of the she...
متن کاملType-tunable amplified spontaneous emission from core-seeded CdSe/CdS nanorods controlled by exciton-exciton interaction.
Type-tunable optical gain performance of core-seeded CdSe/CdS nanorods is studied via two-photon optical pumping. Controlling the exciton-exciton interaction by varying the core and shell size, blue-shifted and red-shifted modes of amplified spontaneous emission are systematically demonstrated and their type attributions are verified by time-resolved emission kinetics.
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- The journal of physical chemistry. B
دوره 110 46 شماره
صفحات -
تاریخ انتشار 2006