Overcoming the bottleneck for quantum computations of complex nanophotonic structures: Purcell and FRET calculations using a rigorous mode hybridization method
Gilles Rosolen, Parry Yu Chen, Bjorn Maes, Yonatan Sivan

TL;DR
This paper introduces a fast, general method for calculating the Green's tensor in complex nanophotonic structures, enabling efficient analysis of Purcell and FRET effects in arbitrarily shaped nanoparticle clusters.
Contribution
It applies a rigorous mode hybridization theory combined with GENOME to efficiently compute Green's tensors for complex nanostructures, including non-trivial shapes, with high accuracy and speed.
Findings
Method accurately predicts Purcell enhancement.
Method accurately predicts FRET rate enhancement.
Significantly faster than direct simulation methods.
Abstract
A calculation of the photonic Green's tensor of a structure is at the heart of many photonic problems, but for non-trivial nanostructures, it is typically a prohibitively time-consuming task. Recently, a general normal mode expansion (GENOME) was implemented to construct the Green's tensor from eigenpermittivity modes. Here, we employ GENOME to the study the response of a cluster of nanoparticles. To this end, we use the rigorous mode hybridization theory derived earlier by D. J. Bergman [Phys. Rev. B 19, 2359 (1979)], which constructs the Green's tensor of a cluster of nanoparticles from the sole knowledge of the modes of the isolated constituent. The method is applied, for the first time, to a scatterer with a non-trivial shape (namely, a pair of elliptical wires) within a fully electrodynamic setting, and for the computation of the Purcell enhancement and F\"{o}rster Resonant Energy…
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