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Register a new userSpontaneous atomic crystallization via diffractive dephasing in optical cavities
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Added by
Adrian Costa-Boquete Mr
Publication date
2020
fields
Physics
and research's language is
English
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The design of an experiment on the spontaneous crystallization of a laser-cooled, but thermal atomic cloud into a hexagonally structured phase is discussed. Atomic interaction is mediated by the dipole potential of an optical lattice formed spontaneously in a multi-mode degenerate cavity from single-mode longitudinal pumping. The length scale of the structure is given by the diffractive dephasing between the spontaneous sidebands and the on-axis pump. A linear stability indicates that the transition can be observed in a cavity of moderate finesse compatible with having the cavity mirrors outside the vacuum cell. A new anti-reflected cell has been assembled for this purpose.
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Strong dipole-exchange interactions due to spontaneously produced contaminant states can trigger rapid dephasing in many-body Rydberg ensembles [E. Goldschmidt et al., PRL 116, 113001 (2016)]. Such broadening has serious implications for many proposals to coherently use Rydberg interactions, particularly Rydberg dressing proposals. The dephasing arises as a runaway process where the production of the first contaminant atoms facilitates the creation of more contaminant atoms. Here we study the time dependence of this process with stroboscopic approaches. Using a pump-probe technique, we create an excess pump Rydberg population and probe its effect with a different probe Rydberg transition. We observe a reduced resonant pumping rate and an enhancement of the excitation on both sides of the transition as atoms are added to the pump state. We also observe a timescale for population growth significantly shorter than predicted by homogeneous mean-field models, as expected from a clustered growth mechanism where high-order correlations dominate the dynamics. These results support earlier works and confirm that the time scale for the onset of dephasing is reduced by a factor which scales as the inverse of the atom number. In addition, we discuss several approaches to minimize these effects of spontaneous broadening, including stroboscopic techniques and operating at cryogenic temperatures. It is challenging to avoid the unwanted broadening effects, but under some conditions they can be mitigated.
The strong light-matter coupling attainable in optical cavities enables the generation of highly squeezed states of atomic ensembles. It was shown in [Phys. Rev. A 66, 022314 (2002)] how an effective one-axis twisting Hamiltonian can be realized in a cavity setup. Here, we extend this work and show how an effective two-axis twisting Hamiltonian can be realized in a similar cavity setup. We compare the two schemes in order to characterize their advantages. In the absence of decoherence, the two-axis Hamiltonian leads to more squeezing than the one-axis Hamiltonian. If limited by decoherence from spontaneous emission and cavity decay, we find roughly the same level of squeezing for the two schemes scaling as (NC)^(1/2) where C is the single atom cooperativity and N is the total number of atoms. When compared to an ideal squeezing operation, we find that for specific initial states, a dissipative version of the one-axis scheme attains higher fidelity than the unitary one-axis scheme or the two-axis scheme. However, the unitary one-axis and two-axis schemes perform better for general initial states.
Quantum light-matter interfaces, based upon ensembles of cold atoms or other quantum emitters, are a vital platform for diverse quantum technologies and the exploration of fundamental quantum phenomena. Most of our understanding and modeling of such systems are based upon macroscopic theories, wherein the atoms are treated as a smooth, quantum polarizable medium. Although it is known that such approaches ignore a number of microscopic details, such as the granularity of atoms, dipole-dipole interactions and multiple scattering of light, the consequences of such effects in practical settings are usually mixed with background macroscopic effects and difficult to quantify. In this work we demonstrate a time-domain method to measure microscopically-driven optical effects in a background-free fashion, by transiently suppressing the macroscopic dynamics. With the method, we reveal a microscopic dipolar dephasing mechanism that generally limits the lifetime of the optical spin-wave order in a random gas. Theoretically, we show the dephasing effect emerges from the strong resonant dipole interaction between close-by atomic pairs.
Atomic systems have long provided a useful material platform with unique quantum properties. The efficient light-matter interaction in atomic vapors has led to numerous seminal scientific achievements including accurate and precise metrology and quantum devices. In the last few decades, the field of thin optical elements with miniscule features has been extensively studied demonstrating an unprecedented ability to control photonic degrees of freedom, both linearly and non-linearly, with applications spanning from photography and spatial light modulators to cataract surgery implants. Hybridization of atoms with such thin devices may offer a new material system allowing traditional vapor cells with enhanced functionality. Here, we fabricate and demonstrate chip-scale, quantum diffractive optical elements which map atomic states to the spatial distribution of diffracted light. Two foundational diffractive elements, lamellar gratings and Fresnel lenses, are hybridized with atomic channels containing hot atomic vapors which demonstrate exceptionally strong frequency dependent behaviors. Providing the design tools for chip-scale atomic diffractive optical elements develops a path for a variety of compact thin quantum-optical elements.
We study the effects of the position of the passive and active cavities on the spontaneous parity-time (PT) symmetry breaking behavior in non-Hermitian coupled cavities array model. We analyze and discuss the energy eigenvalue spectrums and PT symmetry in the topologically trivial and nontrivial regimes under three different cases in detail, i.e., the passive and active cavities are located at, respectively, the two end positions, the second and penultimate positions, and each position in coupled cavities array. The odevity of the number of cavities is further considered to check the effects of the non-Hermitian terms applied on the PT symmetric and asymmetric systems. We find that the position of the passive and active cavities has remarkable impacts on the spontaneous PT symmetry breaking behavior, and in each case the system exhibits distinguishable and novel spontaneous PT symmetry breaking characteristic, respectively. The effects of the non-Hermitian terms on the $mathcal{PT}$ symmetric and asymmetric systems due to the odevity are comparatively different in the first case while qualitatively same in the second case.
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