Atomic dispensers for thermoplasmonic control of alkali vapor pressure in quantum optical applications
Kristina R. Rusimova, Dimitar G. Slavov, Fabienne Pradaux, Joel T. Collins, Sergey N Gordeev, David R. Carbery, W. J. Wadsworth, Peter J. Mosley, Ventsislav Kolev Valev
Alkali metal vapors enable access to single electron systems, suitable for demonstrating fundamental light-matter interactions and promising for quantum logic operations, storage and sensing. However, progress is hampered by the need for robust and repeatable control over the atomic vapor density and over the associated optical depth. Until now, a moderate improvement of the optical depth was attainable through bulk heating or laser desorption - both time-consuming techniques. Here, we use plasmonic nanoparticles to convert light into localized thermal energy and to achieve optical depths in warm vapors, corresponding to a ~16 times increase in vapor pressure in less than 20 ms, with possible reload times much shorter than an hour. Our results enable robust and compact light-matter devices, such as efficient quantum memories and photon-photon logic gates, in which strong optical nonlinearities are crucial.
Alkali metal vapors enable access to single electron systems, suitable for demonstrating fundamental light-matter interactions and promising for quantum logic operations, storage and sensing. However, progress is hampered by the need for robust and repeatable control over the atomic vapor density and over the associated optical depth. Until now, a moderate improvement of the optical depth was attainable through bulk heating or laser desorption - both time-consuming techniques. Here, we use plasmonic nanoparticles to convert light into localized thermal energy and to achieve optical depths in warm vapors, corresponding to a ~16 times increase in vapor pressure in less than 20 ms, with possible reload times much shorter than an hour. Our results enable robust and compact light-matter devices, such as efficient quantum memories and photon-photon logic gates, in which strong optical nonlinearities are crucial.
Integrating alkali atomic vapors with nanophotonic devices offers a scalable route to quantum technologies that leverage strong atom-photon interactions. While there have been many approaches to such integration, the general reliance on traditional glass vapor cells, distilled alkali metals, and epoxy sealing limits reproducibility and scalability. Moreover, mitigating adverse Rb-photonics interactions is essential, particularly as devices become more compact and the alkali source lies in close proximity to the photonic elements. Here, we demonstrate the successful operation of compact and fully integrated devices that combine silicon nitride photonic integrated circuits (PICs) with microfabricated borosilicate vapor cells and pill-type rubidium (Rb) dispensers through hermetic seals via anodic bonding. We show how successful operation hinges on optically activating the dispenser in a low-power pulsed mode, releasing controlled amounts of Rb vapor on demand while mitigating photonic degradation. Simultaneously, a counter-propagating desorption laser completely suppresses Rb-induced losses and enables waveguide-based atomic vapor spectroscopy. Using this approach, we demonstrate repeatable control of vapor density by tuning activation pulse length, duty cycle, and device temperature. These results establish a compact, manufacturable, and scalable vapor-PIC device, and set the stage for future demonstrations in cavity quantum electrodynamics, quantum nonlinear optics, and chip-scale atomic sensors.
Integrating alkali atomic vapors with nanophotonic devices offers a scalable route to quantum technologies that leverage strong atom–photon interactions. While there have been many approaches to such integration, the general reliance on traditional glass vapor cells, distilled alkali metals, and epoxy sealing limits reproducibility and scalability. Moreover, mitigating adverse Rb-photonics interactions is essential, particularly as devices become more compact and the alkali source lies in close proximity to the photonic elements. Here, we demonstrate the successful operation of compact and fully integrated devices that combine silicon nitride photonic integrated circuits (PICs) with microfabricated borosilicate vapor cells and pill-type rubidium (Rb) dispensers through hermetic seals via anodic bonding. We show how successful operation hinges on optically activating the dispenser in a low-power pulsed mode, releasing controlled amounts of Rb vapor on demand while mitigating photonic degradation. Simultaneously, a counter-propagating desorption laser completely suppresses Rb-induced losses and enables waveguide-based atomic vapor spectroscopy. Using this approach, we demonstrate repeatable control of vapor density by tuning activation pulse length, duty cycle, and device temperature. These results establish a compact, manufacturable, and scalable vapor–PIC device, and set the stage for future demonstrations in cavity quantum electrodynamics, quantum nonlinear optics, and chip-scale atomic sensors.
Alkali metal dispensers have become an indispensable tool in the production of atomic vapors for magnetometry, alkali vapor cell clocks, and laser cooling experiments. A primary advantage of these dispensers is that they contain alkali metal in an inert form that can be exposed to air without hazard. However, their high temperature of operation (>600 °C) is undesirable for many applications, as it shifts the atomic speed distribution to higher values and presents a radiative heat source that can raise the temperature of its surroundings. For this reason, dispensers are typically not used in line-of-sight applications, such as atomic beam generation. In this work, we present an integrated rubidium dispenser collimating device with a thickness of only 2 mm that produces a beam of atoms traveling primarily in the forward direction. We find that the collimator plate serves to both shield the dispenser's radiation and moderate the velocity of the atomic beam so that the measured longitudinal speed distribution is comparable to that of an ordinary alkali oven at only a slightly elevated temperature of 200 °C. To confirm our theory, we also constructed another compact apparatus consisting of a dispenser and a silicon collimator and the measurements support our conclusion. Our integrated dispenser collimator will particularly be useful in integrated photonics and cavity QED on-chip, where a localized, directed source of Rb vapor in small quantities is needed.
Over the past decades, alkali atoms have been the subject of intensive and diverse research, ranging from fundamental studies on ultra-cold atoms and Bose-Einstein condensates to technological applications. Since they possess only a single valance s-electron, the alkali atoms manifest a simple low-lying electronic structure compared to other atoms. Moreover, unlike conventional solid state systems their dispersion-free features make them an ideal candidate for sensing applications and referencing tasks. These two features have introduced alkali atoms as promising quantum emitters for the new paradigm of hybrid quantum optics and quantum electrodynamics. This new concept benefits from the existing integrated photonics technology for squeezing and confining the light in sub-wavelength scales to substantially enhance the light-atom interaction. The hybrid chip is envisioned to have light sources, waveguides, devices, and detectors to realize a complex quantum network down to a single photon level. In this talk I will discuss about our recent theoretical and experimental works on atomic vapor spectroscopy in the vicinity of the plasmonic and nanophotonic devices. I start from a density matrix-based formalism describing the evolution of Rb vapor atomic levels, excited with an incoherent pump and coupled to a plasmonic lattice. When designed properly, the lattice plasmon mode efficiently captures the spontaneously emitted photons from the excited Rb atoms and a coherent coupling between the lattice mode and the atomic levels would occur. I will elaborate on the effect of pumping rate and decoherence on the steady state of the hybrid system and the feasibility of achieving a lasing state. In the second part of the talk I will present the results of our experiments on Rb vapor coupled to such a plasmonic lattice. Starting from the pumping mechanism, I describe the collisional scheme we employed to transfer the excited Rb atoms from (_^5)P_(3/2) to(_^5)P_(1/2) , hence achieving a population inversion between P and S levels and an optical gain at 795 nm, eventually. I present the experimental results of this atomic vapor interaction with a plasmonic lattice resonating at 795 nm. The spectroscopy of Rb cloud modified with tightly squeezed and enhanced field of the lattice plasmons shows the clear signature of Fano resonances in the passive gas, followed by amplified spontaneous emission in the active gas and the lasing at higher pumping powers. The results of this study would pave the way toward hybrid atom-quantum photonic chips.
Quantum memories are a crucial technology for enabling large-scale quantum networks through synchronization of probabilistic operations. Such networks impose strict requirements on quantum memory, such as storage time, retrieval efficiency, bandwidth, and scalability. On- and off-resonant ladder protocols on warm atomic vapor platforms are promising candidates, combining efficient high-bandwidth operation with low-noise on-demand retrieval. However, their storage time is severely limited by motion-induced dephasing caused by the broad velocity distribution of atoms composing the vapor. In this paper, we demonstrate velocity selective optical pumping to overcome this decoherence mechanism. This will increase the achievable memory storage time of vapor memories. This technique can also be used for preparing arbitrarily shaped absorption profiles, for instance, preparing an atomic frequency comb absorption feature.
Low-light-level optical nonlinearities are of significant interest for performing operations such as single-photon switching and quantum non-demolition measurements on single-photons. To evoke strong nonlinearities from singlephotons, one can enhance the matter-photon interaction using strongly nonlinear materials such as alkali vapors in combination with an appropriate geometry such as a waveguide, which provides a long interaction length while maintaining a small light mode area. We demonstrate for the first time that such a system can be experimentally realized by loading rubidium vapor inside a hollow-core photonic band-gap fiber. Using the technique of light-induced atomic desorption in this geometry, we have generated optical depths greater than 1000. As a proof of principle, we demonstrate electromagnetically induced transparency (EIT) with control powers 1000 times lower than those used for hot vapor cells in a focused beam geometry. Working with such a high aspect ratio geometry requires us to identify and measure the various sources of decoherence via spectroscopy of desorbed atoms in the fiber. Using such techniques, we also estimate the temperature of the desorbing atoms inside the fiber. The desorption mechanism is studied, and we show that pulsed desorption beams of the right amplitude and duration can be used for generating precisely controlled optical depths. Finally, we investigate the use of various buffer gas techniques for increasing the effective transverse path of the atoms as they move across the fiber in order to reduce their ground state decoherence and map this effect as a function of buffer gas pressure.