A bound state between a quantum emitter (QE) and surface plasmon polaritons (SPPs) can be formed, where the QE is partially stabilized in its excited state. We put forward a general approach for calculating the energy level shift at a negative frequency ω, which is just the negative of the nonresonant part for the energy level shift at positive frequency −ω. We also propose an efficient formalism for obtaining the long-time value of the excited-state population without calculating the eigenfrequency of the bound state or performing a time evolution of the system, in which the probability amplitude for the excited state in the steady limit is equal to one minus the integral of the evolution spectrum over the positive frequency range. With the above two quantities obtained, we show that the non-Markovian decay dynamics in the presence of a bound state can be obtained by the method based on the Green's function expression for the evolution operator. A general criterion for identifying the existence of a bound state is presented. These are numerically demonstrated for a QE located around a nanosphere and in a gap plasmonic nanocavity. These findings are instructive in the fields of coherent light-matter interactions. PACS numbers: 22I.

We put forward a general approach for calculating the quantum energy level shift for emitter in arbitrary nanostructures, in which the energy level shift is expressed by the sum of the real part of the scattering photon Green function (GF) and a simple integral about the imaginary part of the photon GF in the real frequency range without principle value. Compared with the method of direct principal value integral over the positive frequency axis and the method by transferring into the imaginary axis, this method avoids the principle value integral and the calculation of the scattering GF with imaginary frequency. In addition, a much narrower frequency range about the scattering photon GF in enough to get a convergent result. It is numerically demonstrated in the case for a quantum emitter (QE) located around a nanosphere and in a gap plasmonic nanocavity. Quantum dynamics of the emitter is calculated by the time domain method through solving Schrödinger equation in the form of Volterra integral of the second kind and by the frequency domain method based on the Green's function expression for the evolution operator. It is found that the frequency domain method needs information of the scattering GF over a much narrower frequency range. In addition, reversible dynamics is observed. These findings are instructive in the fields of coherent light-matter interactions. PACS numbers: 22I.

Photon Green function (GF) is the vital and most decisive factor in the field of quantum light-matter interaction. It is divergent with two equal space arguments in arbitraryshaped lossy structure and should be regularized. We introduce a finite element method for calculating the regularized GF. It is expressed by the averaged radiation electric field over the finite-size of the photon emitter. For emitter located in homogeneous lossy material, excellent agreement with the analytical results is found for both real cavity model and virtual cavity model. For emitter located in a metal nano-sphere, the regularized scattered GF, which is the difference between the regularized GF and the analytical regularized one in homogeneous space, agrees well with the analytical scattered GF.

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