Abstract
The excited state of colloidal nanoheterostructures consisting of a spherical CdSe nanocrystal with an epitaxially attached CdS rod can be perturbed effectively by electric fields. Field-induced fluorescence quenching coincides with a conversion of the excited state species from the bright exciton to a metastable trapped state (dark exciton) characterized by a power-law luminescence decay. The conversion is reversible so that up to 10% of quenched excitons recombine radiatively post turn-off of a field pulse, increasing the delayed luminescence by a factor of 80. Excitons can be stored for up to times the natural lifetime, opening up applications in optical memory elements.
- Received 11 July 2006
DOI:https://doi.org/10.1103/PhysRevLett.98.017401
©2007 American Physical Society