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Register a new userInteraction signatures and non-Gaussian photon states from a strongly driven atomic ensemble coupled to a nanophotonic waveguide
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We study theoretically a laser-driven one-dimensional chain of atoms interfaced with the guided optical modes of a nanophotonic waveguide. The period of the chain and the orientation of the laser field can be chosen such that emission occurs predominantly into a single guided mode. We find that the fluorescence excitation line shape changes as the number of atoms is increased, eventually undergoing a splitting that provides evidence for the waveguide-mediated all-to-all interactions. Remarkably, in the regime of strong driving the light emitted into the waveguide is non-classical, with a significant negativity of the associated Wigner function. We show that both the emission properties and the non-Gaussian character of the light are robust against voids in the atom chain, enabling the experimental study of these effects with present-day technology. Our results offer a route towards novel types of fiber-coupled quantum light sources and an interesting perspective for probing the physics of interacting atomic ensembles through light.
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We theoretically investigate the quantum scattering of a single-photon pulse interacting with an ensemble of $Lambda$-type three-level atoms coupled to a one-dimensional waveguide. With an effective non-Hermitian Hamiltonian, we study the collective interaction between the atoms mediated by the waveguide mode. In our scheme, the atoms are randomly placed in the lattice along the axis of the one-dimensional waveguide, which closely corresponds to the practical condition that the atomic positions can not be controlled precisely in experiment. Many interesting optical properties occur in our waveguide-atom system, such as electromagnetically induced transparency (EIT) and optical depth. Moreover, we observe that strong photon-photon correlation with quantum beats can be generated in the off-resonant case, which provides an effective candidate for producing non-classical light in experiment. With remarkable progress in waveguide-emitter system, our scheme may be feasible in the near future.
We study the dynamics of a single photon pulse travels through a linear atomic chain coupled to a one-dimensional (1D) single mode photonic waveguide. We derive a time-dependent dynamical theory for this collective many-body system which allows us to study the real time evolution of the photon transport and the atomic excitations. Our analytical result is consistent with previous numerical calculations when there is only one atom. For an atomic chain, the collective interaction between the atoms mediated by the waveguide mode can significantly change the dynamics of the system. The reflectivity of a photon can be tuned by changing the ratio of coupling strength and the photon linewidth or by changing the number of atoms in the chain. The reflectivity of a single photon pulse with finite bandwidth can even approach $100%$. The spectrum of the reflected and transmitted photon can also be significantly different from the single atom case. Many interesting physical phenomena can occur in this system such as the photonic bandgap effects, quantum entanglement generation, Fano-like interference, and superradiant effects. For engineering, this system may serve as a single photon frequency filter, single photon modulation and may find important applications in quantum information.
Planar nanostructures allow near-ideal extraction of emission from a quantum emitter embedded within, thereby realizing deterministic single-photon sources. Such a source can be transformed into M single-photon sources by implementing active temporal-to-spatial mode demultiplexing. We report on the realization of such a demultiplexed source based on a quantum dot embedded in a nanophotonic waveguide. Efficient outcoupling (>60%) from the waveguide into a single mode optical fiber is obtained with high-efficiency grating couplers. As a proof-of-concept, active demultiplexing into M=4 spatial channels is demonstrated by the use of electro-optic modulators with an end-to-end efficiency of >81% into single-mode fibers. Overall we demonstrate four-photon coincidence rates of >1 Hz even under non-resonant excitation of the quantum dot. The main limitation of the current source is the residual population of other exciton transitions that corresponds to a finite preparation efficiency of the desired transition. We quantitatively extract a preparation efficiency of 15% using the second-order correlation function measurements. The experiment highlights the applicability of planar nanostructures as efficient multiphoton sources through temporal-to-spatial demultiplexing and lays out a clear path way of how to scale up towards demonstrating quantum advantages with the quantum dot sources.
We study the dynamics of a single excitation coherently shared amongst an ensemble of atoms and coupled to a one-dimensional wave guide. The coupling between the matter and the light field gives rise to collective phenomena such as superradiant states with an enhanced initial decay rate, but also to the coherent exchange of the excitation between the atoms. We find that the competition between the two phenomena provides a characteristic dynamics for the decay of the excitations, and remarkably exhibits an algebraic behavior, instead of the expected standard exponential one, for a large number of atoms. The analysis is first performed for a chiral waveguide, where the problem can be solved analytically, and then is extended to the bidirectional waveguide.
Single particle-resolved fluorescence imaging is an enabling technology in cold-atom physics. However, so far, this technique was not available for nanophotonic atom-light interfaces. Here, we image single atoms that are trapped and optically interfaced using an optical nanofiber. Near-resonant light is scattered off the atoms and imaged while counteracting heating mechanisms via degenerate Raman cooling. We detect trapped atoms within 150 ms and record image sequences of given atoms. Building on our technique, we perform two experiments which are conditioned on the number and position of the nanofiber-trapped atoms. We measure the transmission of nanofiber-guided resonant light and verify its exponential scaling in the few-atom limit, in accordance with Beer-Lamberts law. Moreover, depending on the interatomic distance, we observe interference of the fields that two simultaneously trapped atoms emit into the nanofiber. The demonstrated technique enables post-selection and possible feedback schemes and thereby opens the road towards a new generation of experiments in quantum nanophotonics.
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