We have developed a theory for the photoluminescence and absorption coefficient in nanohybrids made of an ensemble of metallic nanoparticles and the core-shell quantum emitter. The core-shell quantum emitter is made of a quantum emitter core and a dielectric shell. When a probe laser light falls on metallic nanoparticles, electric dipoles are induced in the ensemble. Hence, these dipoles interact with each other via the dipole-dipole interaction. The surface plasmon polaritons are also present in metallic nanoparticles. Excitons in the quantum emitter interact with these surface plasmon polaritons and the dipole-dipole interaction electric fields. Using the quantum mechanical density matrix method, we have developed a theory for the photoluminescence quenching and enhancement, the nonradiative decay rate, and the absorption coefficient for the quantum emitter in the ensemble of metallic nanoparticles. We showed that the nonradiative energy loss is mainly due to the exciton coupling with the dipole-dipole interaction and it is responsible for the power loss in the quantum emitter. This in turn produces anomalous photoluminescence enhancement and quenching. We have compared our theory with experimental data of core-shell CdSe/ZnS quantum dots embedded in an ensemble of Au nanoparticles. A good agreement between theory and experiment is found. We showed that there are an energy shift and an enhancement in the absorption peak due to the dipole-dipole interaction. Finally, we showed that there is the anomalous quenching and enhancement in the photoluminescence spectrum of the CdSe/ZnS quantum dot embedded in the ensemble of Au nanoparticles. This phenomenon also occurs mainly due to the dipole-dipole interaction in the ensemble of Au nanoparticles. These are interesting results and can be used to fabricate nanosensors for applications in nanomedicine and nanotechnology.
|Titolo:||Anomalous Photoluminescence Quenching in Metallic Nanohybrids|
|Data di pubblicazione:||2019|
|Appare nelle tipologie:||1.1 Articolo in rivista|