Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userRobust stability of quantum interference realized by coexisting detuned and resonant STIRAPs
81
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
Inspired by a recent experiment [Phys. Rev. Letts. textbf{122}, 253201(2019)] that an unprecedented quantum interference was observed in the way of Stimulated Raman adiabatic passage (STIRAP) due to the coexisting resonant- and detuned-STIRAPs, we comprehensively study this effect for uncovering its robustness towards the external-field fluctuations of laser noise, imperfect resonance condition as well as the excited-state decaying. We verify that, an auxiliary dynamical phase accumulated in hold time caused by the quasi-dark state can sensitively manipulate the visibility and frequency of the interference fringe, representing a new hallmark to measure the hyperfine energy accurately. The robust stability of scheme comes from the intrinsic superiority embedded in STIRAP itself, which promises a remarkable preservation of the quantum interference quality in a practical implementation.
rate research
Read More
Magnetic control of reactive scattering is realized in an ultracold mixture of $^{23}$Na atoms and $^{23}$Na$^{6}$Li molecules via Feshbach resonances. In most molecular systems, particles form lossy collision complexes at short range with unity probability for chemical reaction or inelastic scattering leading to the so-called universal loss rate. In contrast, Na${+}$NaLi is shown to have ${<}4%$ loss probability at short range when spin polarization suppresses loss. By controlling the phase of the wavefunction via a Feshbach resonance, we modify the loss rate by more than a factor of hundred, from far below the universal limit to far above, demonstrated here for the fist time. The results are explained in analogy with an optical Fabry-Perot interferometer by constructive and destructive interference of reflections at short and long range. Our work demonstrates quantum control of chemistry by magnetic fields with the full dynamic range predicted by our models.
Stimulated Raman adiabatic passage (STIRAP) allows to efficiently transferring the populations between two discrete quantum states and has been used to prepare molecules in their rovibrational ground state. In realistic molecules, a well-resolved intermediate state is usually selected to implement the resonant STIRAP. Due to the complex molecular level structures, the detuned STIRAP always coexists with the resonant STIRAP and may cause unexpected interference phenomenon. However, it is generally accepted that the detuned STIRAP can be neglected if compared with the resonant STIRAP. Here we report on the first observation of interference between the resonant and detuned STIRAP in the adiabatic creation of $^{23}$Na$^{40}$K ground-state molecules. The interference is identified by observing that the number of Feshbach molecules after a round-trip STIRAP oscillates as a function of the hold time, with a visibility of about 90%. This occurs even if the intermediate excited states are well resolved, and the single-photon detuning of the detuned STIRAP is about one order of magnitude larger than the linewidth of the excited state and the Rabi frequencies of the STIRAP lasers. Moreover, the observed interference indicates that if more than one hyperfine level of the ground state is populated, the STIRAP prepares a coherent superposition state among them, but not an incoherent mixed state. Further, the purity of the hyperfine levels of the created ground state can be quantitatively determined by the visibility of the oscillation.
We theoretically investigate the process of coupling cold atoms into the core of a hollow-core photonic-crystal optical fiber using a blue-detuned Laguerre-Gaussian beam. In contrast to the use of a red-detuned Gaussian beam to couple the atoms, the blue-detuned hollow-beam can confine cold atoms to the darkest regions of the beam thereby minimizing shifts in the internal states and making the guide highly robust to heating effects. This single optical beam is used as both a funnel and guide to maximize the number of atoms into the fiber. In the proposed experiment, Rb atoms are loaded into a magneto-optical trap (MOT) above a vertically-oriented optical fiber. We observe a gravito-optical trapping effect for atoms with high orbital momentum around the trap axis, which prevents atoms from coupling to the fiber: these atoms lack the kinetic energy to escape the potential and are thus trapped in the laser funnel indefinitely. We find that by reducing the dipolar force to the point at which the trapping effect just vanishes, it is possible to optimize the coupling of atoms into the fiber. Our simulations predict that by using a low-power (2.5 mW) and far-detuned (300 GHz) Laguerre-Gaussian beam with a 20-{mu}m radius core hollow-fiber it is possible to couple 11% of the atoms from a MOT 9 mm away from the fiber. When MOT is positioned further away, coupling efficiencies over 50% can be achieved with larger core fibers.
Using the z-scan technique, we have measured the self-induced absorptive and refractive nonlinear behavior of hot atomic rubidium vapor within the Doppler profile of the D2 line. We observe large nonlinear amplitude and phase effects with only tens of microwatts of incident power. Our results are in good agreement with numerical calculations based on an analytic model of a Doppler- broadened two-level system.
Photon-mediated coupling between distant matter qubits may enable secure communication over long distances, the implementation of distributed quantum computing schemes, and the exploration of new regimes of many-body quantum dynamics. Nanophotonic devices coupled to solid-state quantum emitters represent a promising approach towards realization of these goals, as they combine strong light-matter interaction and high photon collection efficiencies. However, the scalability of these approaches is limited by the frequency mismatch between solid-state emitters and the instability of their optical transitions. Here we present a nano-electromechanical platform for stabilization and tuning of optical transitions of silicon-vacancy (SiV) color centers in diamond nanophotonic devices by dynamically controlling their strain environments. This strain-based tuning scheme has sufficient range and bandwidth to alleviate the spectral mismatch between individual SiV centers. Using strain, we ensure overlap between color center optical transitions and observe an entangled superradiant state by measuring correlations of photons collected from the diamond waveguide. This platform for tuning spectrally stable color centers in nanophotonic waveguides and resonators constitutes an important step towards a scalable quantum network.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
