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 1μs field pulse, increasing the delayed luminescence by a factor of 80. Excitons can be stored for up to 105 times the natural lifetime, opening up applications in optical memory elements. © 2007 The American Physical Society.
| Original language | English |
|---|---|
| Article number | 17401 |
| Journal | Physical Review Letters |
| Volume | 98 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 2007 |
| Externally published | Yes |
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