The dipole emission rate inside a hollow resonator with high quality factor Q, which forms a nano quantum dot system is analysed in this paper. The structure modes are firstly quantised, allowing the position-dependent dipole emission rate to be evaluated. In particular, in the nanoscale limit, we show that the dipole emission rate process is can be only produced by a fundamental mode of the system. The effect of the nanoscale limit has been demonstrated to dramatically increase the dipole emission rate. The result is illustrated with reference to sodium atoms placed inside a nano quantum dot resonator with rectangular cross section.
The dipole emission rate inside a hollow resonator with high quality factor Q, which forms a nano quantum dot system is analysed in this paper. The structure modes are firstly quantised, allowing the position-dependent dipole emission rate to be evaluated. In particular, in the nanoscale limit, we show that the dipole emission rate process is can be only produced by a fundamental mode of the system. The effect of the nanoscale limit has been demonstrated to dramatically increase the dipole emission rate. The result is illustrated with reference to sodium atoms placed inside a nano quantum dot resonator with rectangular cross section.
Abstract. We present a general formalism for studying the emission rate of an atom inside a high Q-factor quantum cylindrical resonator. The electromagnetic field structure inside such closed resonator is de-rived. Then the cavity modes are quantised, allowing the position-dependent atomic emission rate to be calculated. Depending on the circumstances, the atomic emission rate may be increased or reduced, and in extreme cases is completely suppressed. Especially, in the quantum size system, the atomic emission rate is possible only via a few cavity modes. The calculations are carried out for the sodium atoms immersed in an empty quantum size resonator. 1.
Atomic decay rate process of an excited two-level atom placed inside a cylindrical quantum nanotube is investigated. In particular, when a hole diameter of the cylindrical tube of the order of nanoscale, only the lowest order mode can exist, which means that the system operates as an exact single mode structure. The structure modes are quantised, allowing the position-dependent atomic decay rate process to be evaluated. For an atom inside a cylindrical structure whose typical dimension is in the nanoscale the atomic decay rate process is enhanced compared with that of the same atom in the free space.
Dipole-dipole interaction between two two-level `atoms' in photonic crystal nanocavity is investigated based on finite-difference time domain algorithm. This method includes both real and virtual photon effects and can be applied for dipoles with different transition frequencies in both weak and strong coupling regimes. Numerical validations have been made for dipoles in vacuum and in an ideal planar microcavity. For dipoles located in photonic crystal nanocavity, it is found that the cooperative decay parameters and the dipole-dipole interaction potential strongly depend on the following four factors: the atomic position, the atomic transition frequency, the resonance frequency, and the cavity quality factor. Properly arranging the positions of the two atoms, we can acquire equal value of the cooperative decay parameters and the local coupling strength. Large cooperative decay parameters can be achieved when transition frequency is equal to the resonance frequency. For transition frequency varying in a domain of the cavity linewidth around the resonance frequency, dipole-dipole interaction potential changes continuously from attractive to repulsive case. Larger value and sharper change of cooperative parameters and dipole-dipole interaction can be obtained for higher quality factor. Our results provide some manipulative approaches for dipole-dipole interaction with potential application in various fields such as quantum computation and quantum information processing based on solid state nanocavity and quantum dot system.
Cavity quantum electrodynamics is the art of enhancing light-matter interaction of photon emitters in cavities with opportunities for sensing, quantum information, and energy capture technologies. To boost emitter-cavity interaction, that is, coupling strength g, ultrahigh quality cavities have been concocted yielding photon trapping times of microsecondsy to milliseconds. However, such high- Q cavities give poor photon output, hindering applications. To preserve high photon output, it is advantageous to strive for highly localized electric fields in radiatively lossy cavities. Nanophotonic antennas are ideal candidates combining low- Q factors with deeply localized mode volumes, allowing large g, provided the emitter is positioned exactly right inside the nanoscale mode volume. Here, with nanometer resolution, we map and tune the coupling strength between a dipole nanoantenna-cavity and a single molecule, obtaining a coupling rate of g max ∼ 200 GHz. Together with accelerated single photon output, this provides ideal conditions for fast and pure nonclassical single photon emission with brightness exceeding 10 9 photons/sec. Clearly, nanoantennas acting as “bad” cavities offer an optimal regime for strong coupling g to deliver bright on-demand and ultrafast single photon nanosources for quantum technologies.
The effects of light absorption and amplification on the transition rates of the electric-dipole emission of atoms or molecules embedded in micrometer-sized dielectric spheres are investigated in the framework of classical electrodynamics. The expression for the form factor of a resonant emission line is derived. Its dependence on the imaginary part of the light’s refractive index is investigated. It is discovered that the active sphere does not act as an optical resonator if light amplification is strong.
Semiconductor quantum dots (QDs) are commonly considered as artificial atoms due to the 3D confinement of the electrons. These nanostructures are very promising for the realization of integrated devices such as single photon sources for quantum cryptography applications [1,2]. However, contrarily to genuine atoms, QDs are condensed matter systems and they consequently suffer from the coupling to their environment [3] which degrades the quality of the emitted photons in view of quantum cryptography applications. One way to circumvent this coupling is to excite strictly resonantly the QD at low temperature [4-10]. This difficult task has been achieved by designing an original excitation scheme to spatially decouple the excitation and detection paths. We first report that experimental studies of the resonant emission (RE) of single QDs can be strongly limited, even impossible, since most of the QDs show a very strong quenching of the RE of the fundamental transition. This issue is a broadly met experimental situation which is highly problematic for cavity quantum electrodynamics experiments in single QDs. We propose an efficient way to overcome this issue based on the use of an ultra-weak non-resonant laser that optically gates the QD RE [8] which controls the residual doping inherent to the QDs fabrication. It induces a complete recovery of the properties of an artificial atom, and the single QDs behave as quasi-ideal two-level systems. Up to now [7,9], the measurements on the QDs RE reported in the literature mainly focus on the incoherent fluorescence signal for achieving efficient single photon emission. In this regime, the spectrum linewidth is always limited to the radiative limit. We present experimental studies on the coherent laser light scattering by a single QD [7]. Besides the antibunching effect showing the non-classical nature of the emitted light, we observe that the QD emission spectrum is determined by the spectrum of the resonant excitation laser. By reducing the resonant excitation power, the so-called Mollow triplet shrinks to a single narrow Lorentzian line, while the relative intensity of this narrow peak increases and tends to overwhelm the RE spectrum. This implies that single QDs can produce single photons with a coherence time that is not limited anymore by the QD electronic properties, resulting in what we name an " ultra-coherent " character [7]. In conclusion, the resulting ultra-coherent single photon source promises high degrees of indistinguishability of the emitted photons which is a crucial requirement for quantum information applications. References [1] P. Michler et al., Science 290 (2000). [6] S. Ates et al., PRL 103 (2009). [2] C. Santori et al., Nature 419 (2002). [7] H. S. Nguyen et al., APL 99 (2011). [3] A. Berthelot et al., Nat. Phys. 2 (2006). [8] H. S. Nguyen et al., PRL 108 (2012). [4] A. Muller et al., PRL 99 (2007). [9] C. Matthiesen et al., PRL 1082 (2012). [5] R. Melet et al., PRB 78 (2008). [10] A. Reinhard et al., Nat. Phot. 6 (2012).