Dipole-dipole interaction between a quantum dot and graphene nanodisk
Joel D. Cox, Mahi R. Singh, Godfrey Gumbs, Miguel. A. Ant\'on and, Fernando Carre\~no

TL;DR
This paper theoretically investigates the dipole-dipole interaction and energy transfer between a quantum dot and graphene nanodisk within a nonlinear photonic crystal, demonstrating controllable energy transfer and potential applications in nano-devices.
Contribution
It introduces a model for controlling energy transfer in a hybrid quantum dot-graphene system using a nonlinear photonic crystal and external fields, highlighting tunable interactions.
Findings
Energy transfer peaks correspond to dressed excitons in the quantum dot.
Energy transfer can be switched on and off via external control.
Peak characteristics are adjustable by graphene layers and separation distance.
Abstract
We study theoretically the dipole-dipole interaction and energy transfer in a hybrid system consisting of a quantum dot and graphene nanodisk embedded in a nonlinear photonic crystal. In our model a probe laser field is applied to measure the energy transfer between the quantum dot and graphene nanodisk while a control field manipulates the energy transfer process. These fields create excitons in the quantum dot and surface plasmon polaritons in the graphene nanodisk which interact via the dipole-dipole interaction. Here the nonlinear photonic crystal acts as a tunable photonic reservoir for the quantum dot, and is used to control the energy transfer. We have found that the spectrum of power absorption in the quantum dot has two peaks due to the creation of two dressed excitons in the presence of the dipole-dipole interaction. The energy transfer rate spectrum of the graphene nanodisk…
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
