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Bistable optical response of nanoparticle heterodimer: Mechanism, phase diagram, and switching time

Authors :
Nugroho, B. S.
Iskandar, A. A.
Malyshev, V. A.
Knoester, J.
Source :
J. Chem. Phys. 139, 014303 (2013)
Publication Year :
2012

Abstract

We conduct a theoretical study of the bistable optical response of a nanoparticle heterodimer comprised of a closely spaced semiconductor quantum dot and metal nanoparticle. The bistable nature of the response results from the interplay between the quantum dot's optical nonlinearity and its self-action (feedback) originating from the presence of the metal nanoparticle. We show that the feedback is governed by a complex valued coupling parameter $G$. Both the real and imaginary parts of $G$ ($G_\mathrm{R}$ and $G_\mathrm{I}$) play an important role in the occurrence of bistability, which is manifested in an S-shaped dependence of the quantum dot excited state population on the intensity of the external field, and hysteresis of the population. From our calculations, we find that at $G_\mathrm{R} = 0$, the critical value for bistability to occur is $G_\mathrm{I} = 8\Gamma$, whereas at $G_\mathrm{I} = 0$, the critical value of $G_\mathrm{R} = 4\Gamma$, where $\Gamma$ is the polarization dephasing rate. Thus, there exist two different (limiting) mechanisms of bistability, depending on whether $G_\mathrm{R}$ is much larger or much smaller than $G_\mathrm{I}$. We also calculate the bistability phase diagram within the system's parameter space: spanned by $G_\mathrm{R}$, $G_\mathrm{I}$ and $\Delta$, the latter being the detuning between the driving frequency and the transition frequency of the quantum dot. Additionally, switching times from the lower stable branch to the upper one (and {\it vise versa}) are calculated as a function of the intensity of the driving field. We show that the conditions for bistability to occur can be realized, for example, for a heterodimer comprised of a closely spaced CdSe (or CdSe/ZnSe) quantum dot and a gold nanosphere.<br />Comment: 9 pages, 6 figures

Details

Database :
arXiv
Journal :
J. Chem. Phys. 139, 014303 (2013)
Publication Type :
Report
Accession number :
edsarx.1209.3255
Document Type :
Working Paper
Full Text :
https://doi.org/10.1063/1.4811181