Spontaneous Emission Decay and Excitation in Photonic Time Crystals
Jagang Park, Kyungmin Lee, Ruo-Yang Zhang, Hee Chul Park, Jung-Wan Ryu, Gil Young Cho, Min Yeul Lee, Zhao-Qing Zhang, Namkyoo Park, Wonju Jeon, Jonghwa Shin, Che Ting Chan, Bumki Min
Over the last few decades, the predominant strategies for controlling spontaneous emission have involved tailoring the spatial surroundings of quantum emitters or atoms to create resonant or spatially periodic photonic structures. However, the rise of time-varying photonics has prompted a reevaluation of spontaneous emission in dynamically changing environments, especially within photonic time crystals, where optical properties undergo time-periodic modulation. Here, we apply classical light-matter interaction theory together with Floquet analysis to reveal a substantial enhancement of the spontaneous emission decay rate at the momentum gap frequency in photonic time crystals. Moreover, our findings suggest that photonic time crystals enable a nonequilibrium light-matter interaction process: the spontaneous excitation of an atom from its ground state to an excited state, accompanied by the concurrent emission of a photon, referred to as spontaneous emission excitation.
Over the last few decades, the predominant strategies for controlling spontaneous emission have involved tailoring the spatial surroundings of quantum emitters or atoms to create resonant or spatially periodic photonic structures. However, the rise of time-varying photonics has prompted a reevaluation of spontaneous emission in dynamically changing environments, especially within photonic time crystals, where optical properties undergo time-periodic modulation. Here, we apply classical light-matter interaction theory together with Floquet analysis to reveal a substantial enhancement of the spontaneous emission decay rate at the momentum gap frequency in photonic time crystals. Moreover, our findings suggest that photonic time crystals enable a nonequilibrium light-matter interaction process: the spontaneous excitation of an atom from its ground state to an excited state, accompanied by the concurrent emission of a photon, referred to as spontaneous emission excitation.
Photonic time crystals host a variety of intriguing phenomena, from wave amplification and mixing to exotic band structures, all stemming from the time-periodic modulation of optical properties. While these features have been well described classically, their quantum manifestation when coupled to an atomic electric dipole has remained elusive. Here, we introduce a quantum electrodynamical model of photonic time crystals that reveals a deeper connection between classical and quantum pictures: the classical momentum gap arises from a localization-delocalization quantum phase transition in a Floquet-photonic synthetic lattice. Leveraging an effective Hamiltonian perspective, we pinpoint the critical momenta and highlight how classical exponential field growth manifests itself as wave-packet acceleration in the quantum synthetic space. Remarkably, when a two-level atom is embedded in such a photonic time crystal, its Rabi oscillations undergo irreversible decay to a half-and-half mixed state-a previously unobserved phenomenon driven by photonic delocalization within the momentum gap, even with just a single frequency mode. Our findings establish photonic time crystals as versatile platforms for studying nonequilibrium quantum photonics and suggest new avenues for controlling light matter interactions through time domain engineering.
We consider the spontaneous emission of a two-level quantum emitter, such as an atom or a quantum dot, in a modulated time-dependent environment with a photonic band gap. An example of such an environment is a dynamical photonic crystal or any other environment with a band gap whose properties are modulated in time, in the effective mass approximation. After introducing our model of a dynamical photonic crystal, we show that it allows new possibilities to control and tailor the physical features of the emitted radiation, specifically its frequency spectrum. In the weak-coupling limit and in an adiabatic case, we obtain the emitted spectrum and we show the appearance of two lateral peaks due to the presence of the modulated environment, separated from the central peak by the modulation frequency. We show that the two side peaks are not symmetric in height, and that their height ratio can be exploited to investigate the density of states of the environment. Our results show that a dynamical environment can give further possibilities to modify the spontaneous emission features, such as its spectrum and emission rate, with respect to a static one. Observability of the phenomena we obtain is discussed, as well as relevance for tailoring and engineering radiative processes.
Chapter 1 IntroductionUltimate inhibition of spontaneous emission can be achieved in artificial periodic structures with tailor-made forbidden frequency bands [5].These periodic structures known as photonic crystals consist of different dielectric materials, where the index of refraction varies on length scales comparable to the wavelength of light.Therefore, the periodicity of photonic crystals is about 1000 times as large as that of atomic crystals.Light with specific frequencies is forbidden to propagate along certain directions by wave interference, similarly to Bragg diffraction of x-rays in atomic crystals.Such forbidden frequency ranges are called stopgaps.The larger the contrast of the refractive index between the two materials of a photonic crystal, the more strongly light is influenced, and the broader the stopgaps become.It was predicted in 1987 that an extreme situation may be feasible when light cannot propagate along any direction [6, 7].This situation is called a photonic bandgap.Spontaneous emission is completely inhibited for frequencies inside such a bandgap and, conversely, strongly enhanced for frequencies outside the bandgap.Photonic crystals, therefore, provide an ultimate tool for manipulating with light, which is of extreme interest for scientists and engineers [8, 9].Recent advances in nanotechnology have resulted in ability to synthesize semiconductor structures with dimensions of a few nanometers.Due to the finite sizes, electron-hole pairs (excitons) can be confined in these nanostructures, which leads to discrete excitonic energy levels.The nanocrystals that confine excitons in spherical or circular spaces are known as quantum dots.The discrete structure of the energy levels results in advantageous optical properties of these nanocrystals: narrow and tunable emission spectra.The emission frequencies can be tuned by varying the nanocrystal size: the smaller the size, the higher the emission frequency.These properties make the nanocrystals very promising elementary emitters for new experiments and devices [10, 11]. Outline of the thesisThis thesis describes time-and angle-resolved experiments, in which effects of threedimensional (3D) photonic crystals on spontaneous emission of embedded light sources (quantum dots and dye molecules) were studied.The thesis is organized as follows:In Chapter 2 we review the theoretical basics of the interaction between light and matter.We discuss the factors triggering the process of spontaneous emission and consider in detail the time evolution of the excited state of the emitter that interacts with the quantized 1.
Impressive progress has been achieved in controlling the spontaneous emission rate for emitters in Nanophotonic structures, such as microcavities, photonic crystals and nano-antennas. In all cases, however, the modification of the emission is stationary in time. Thus, the emission rate is time-independent and the distribution of photon emission times are stochastic and follow an exponential distribution in the weak coupling regime. In this paper, by using fast all-optical switching of a microcavity, the cavity resonance is tuned within tens of picosesonds. This drastically changes the local optical density of states at the emission frequency within the emission lifetime of the emitters. This paper theoretically studied an ensemble of two-level sources with a time dependent decay rate and have derived the excited state population and emitted intensity as a function of time for continuous wave and pulsed excitation. Deterministic bursts of dramatically enhanced or inhibited emission intensity within short intervals. Thereby, we control the photon distribution to show behavior that strongly deviates from single exponential decay. This can be used to protect quantum information systems against decoherence and to realize non-Markovian dynamics in cavity quantum electrodynamics.
Spontaneous emission is one of the most fundamental out-of-equilibrium processes in which an excited quantum emitter relaxes to the ground state due to quantum fluctuations. In this process, a photon is emitted that can interact with other nearby emitters and establish quantum correlations between them, e.g., via super and subradiance effects. One way to modify these photon-mediated interactions is to alter the dipole radiation patterns of the emitter, e.g., by placing photonic crystals near them. One recent example is the generation of strong directional emission patterns - key to enhancing super and subradiance effects - in two dimensions by employing photonic crystals with band structures characterized by linear isofrequency contours and saddle points. However, these studies have predominantly used oversimplified toy models, overlooking the electromagnetic field's intricacies in actual materials, including aspects like geometrical dependencies, emitter positions, and polarization. Our study delves into the interaction between these directional emission patterns and the variables mentioned above, revealing the untapped potential to fine-tune collective quantum optical phenomena.
Spontaneous emission is one of the most fundamental out-of-equilibrium processes in which an excited quantum emitter relaxes to the ground state due to quantum fluctuations. In this process, a photon is emitted that can interact with other nearby emitters and establish quantum correlations between them, e.g., via super and subradiance effects. One way to modify these photon-mediated interactions is to alter the dipole radiation patterns of the emitter, e.g., by placing photonic crystals near them. One recent example is the generation of strong directional emission patterns-key to enhancing super and subradiance effects-in two dimensions by employing photonic crystals with band structures characterized by linear isofrequency contours and saddle-points. However, these studies have predominantly used oversimplified toy models, overlooking the electromagnetic field's intricacies in actual materials, including aspects like geometrical dependencies, emitter positions, and polarization. Our study delves into the interaction between these directional emission patterns and the aforementioned variables, revealing the untapped potential to fine-tune collective quantum optical phenomena.