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Register a new userTransporting long-lived quantum spin coherence in a photonic crystal fiber
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Confining particles in hollow-core photonic crystal fibers has opened up new prospects to scale up the distance and time over which particles can be made to interact with light. However, maintaining long-lived quantum spin coherence and/or transporting it over macroscopic distances in a waveguide remain challenging. Here, we demonstrate coherent guiding of ground-state superpositions of 85Rb atoms over a centimeter range and hundreds of milliseconds inside a hollow-core photonic crystal fiber. The decoherence is mainly due to dephasing from residual differential light shift (DLS) from the optical trap and the inhomogeneity of ambient magnetic field. Our experiment establishes an important step towards a versatile platform that can lead to applications in quantum information networks and matter wave circuit for quantum sensing.
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Coherent interactions between electromagnetic and matter waves lie at the heart of quantum science and technology. However, the diffraction nature of light has limited the scalability of many atom-light based quantum systems. Here, we use the optical fields in a hollow-core photonic crystal fiber to spatially split, reflect, and recombine a coherent superposition state of free-falling 85Rb atoms to realize an inertia-sensitive atom interferometer. The interferometer operates over a diffraction-free distance, and the contrasts and phase shifts at different distances agree within one standard error. The integration of phase coherent photonic and quantum systems here shows great promise to advance the capability of atom interferometers in the field of precision measurement and quantum sensing with miniature design of apparatus and high efficiency of laser power consumption.
We study the mutual interaction between two identical quantum dots coupled to the normal modes of two-site photonic crystal molecules in a planar waveguide geometry, i.e. photonic crystal dimers. We find that the radiative coupling between the two quantum emitters is maximized when they are in resonance with either the bonding or the antibonding modes of the coupled cavity system. Moreover, we find that such effective interdot coupling is sizable, in the meV range, and almost independent from the cavities distance, as long as a normal mode splitting exceeding the radiative linewidth can be established (strong cavity-cavity coupling condition). In realistic and high quality factor photonic crystal cavity devices, such distance can largely exceed the emission wavelength, which is promising for long distance entanglement generation between two qubits in an integrated nanophotonic platform. We show that these results are robust against position disorder of the two quantum emitters within their respective cavities.
This article offers an extensive survey of results obtained using hybrid photonic crystal fibers (PCFs) which constitute one of the most active research fields in contemporary fiber optics. The ability to integrate novel and functional materials in solid- and hollow-core PCFs through various post-processing methods has enabled new directions towards understanding fundamental linear and nonlinear phenomena as well as novel application aspects, within the fields of optoelectronics, material and laser science, remote sensing and spectroscopy. Here the recent progress in the field of hybrid PCFs is reviewed from scientific and technological perspectives, focusing on how different fluids, solids and gases can significantly extend the functionality of PCFs. In the first part of this review we discuss the most important efforts by research groups around the globe to develop tunable linear and nonlinear fiber-optic devices using PCFs infiltrated with various liquids, glasses, semiconductors and metals. The second part is concentrated on the most recent and state-of-the-art advances in the field of gas-filled hollow-core PCFs. Extreme ultrafast gas-based nonlinear optics towards light generation in the extreme wavelength regions of vacuum ultraviolet (VUV), pulse propagation and compression dynamics in both atomic and molecular gases, and novel soliton - plasma interactions are reviewed. A discussion of future prospects and directions is also included.
Atomic lattice clocks have spurred numerous ideas for tests of fundamental physics, detection of general relativistic effects, and studies of interacting many-body systems. On the other hand, molecular structure and dynamics offer rich energy scales that are at the heart of new protocols in precision measurement and quantum information science. Here we demonstrate a fundamentally distinct type of lattice clock that is based on vibrations in diatomic molecules, and present coherent Rabi oscillations between weakly and deeply bound molecules that persist for 10s of milliseconds. This control is made possible by a state-insensitive magic lattice trap that weakly couples to molecular vibronic resonances and enhances the coherence time between molecules and light by several orders of magnitude. The achieved quality factor $Q=8times10^{11}$ results from 30-Hz narrow resonances for a 25-THz clock transition in Sr$_2$. Our technique of extended coherent manipulation is applicable to long-term storage of quantum information in qubits based on ultracold polar molecules, while the vibrational clock enables precise probes of interatomic forces, tests of Newtonian gravitation at ultrashort range, and model-independent searches for electron-to-proton mass ratio variations.
The electron spin coherence in n-doped and undoped, self-assembled CdSe/Zn(S,Se) quantum dots has been studied by time-resolved pump-probe Kerr rotation. Long-lived spin coherence persisting up to 13 ns after spin orientation has been found in the n-doped quantum dots, outlasting significantly the lifetimes of charge neutral and negatively charged excitons of 350 - 530 ps. The electron spin dephasing time as long as 5.6 ns has been measured in a magnetic field of 0.25 T. Hyperfine interaction of resident electrons with a nuclear spin fluctuations is suggested as the main limiting factor for the dephasing time. The efficiency of this mechanism in II-VI and III-V quantum dots is analyzed.
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