No Arabic abstract
We show how a single linearly polarized control field can produce a sharply tunable group velocity of a weak probe field at resonance in a four-level atomic configuration of alkali vapors. The dispersion can be switched from normal to anomalous along with vanishing absorption, just by changing intensity of the resonant control field. In addition, by allowing different intensities of the different polarization components of the control field, the anomalous dispersion can be switched back to the normal. This thereby creates a valley of anomaly in group index variation and offers two sets of control field intensities, for which the system behaves like a vacuum. The explicit analytical expressions for the probe coherence are provided along with all physical explanations. We demonstrate our results in $J = 1/2 leftrightarrow J = 1/2$ transition for D_1 lines in alkali atoms, in which one can obtain a group index as large as $3.2times10^{8}$ and as negative as $-1.5times10^{5}$ using a control field with power as low as 0.017 mW/cm$^2$ and 9.56 mW/cm$^2$ .
Ultralow-power diode-laser radiation is employed to induce photodesorption of cesium from a partially transparent thin-film cesium adsorbate on a solid surface. Using resonant Raman spectroscopy, we demonstrate that this photodesorption process enables an accurate local optical control of the density of dimer molecules in alkali-metal vapors.
An electrically-controllable, solid-state, reversible device for sourcing and sinking alkali vapor is presented. When placed inside an alkali vapor cell, both an increase and decrease of the rubidium vapor density by a factor of two are demonstrated through laser absorption spectroscopy on 10 to 15 s time scales. The device requires low voltage (5 V), low power (<3.4 mW peak power), and low energy (<10.7 mJ per 10 s pulse). The absence of oxygen emission during operation is shown through residual gas analysis, indicating Rb is not lost through chemical reaction but rather by ion transport through the designed channel. This device is of interest for atomic physics experiments and, in particular, for portable cold-atom systems where dynamic control of alkali vapor density can enable advances in science and technology.
Quantum memories are a crucial technology for enabling large-scale quantum networks through synchronisation 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 vapour 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 comprising the vapour. In this paper, we demonstrate velocity selective optical pumping to overcome this decoherence mechanism. This will increase the achievable memory storage time of vapour memories. This technique can also be used for preparing arbitrarily shaped absorption profiles, for instance, preparing an atomic frequency comb absorption feature.
Precision sensing, and in particular high precision magnetometry, is a central goal of research into quantum technologies. For magnetometers, often trade-offs exist between sensitivity, spatial resolution, and frequency range. The precision, and thus the sensitivity of magnetometry, scales as $1/sqrt {T_2}$ with the phase coherence time, $T_2$, of the sensing system playing the role of a key determinant. Adapting a dynamical decoupling scheme that allows for extending $T_2$ by orders of magnitude and merging it with a magnetic sensing protocol, we achieve a measurement sensitivity even for high frequency fields close to the standard quantum limit. Using a single atomic ion as a sensor, we experimentally attain a sensitivity of $4.6$ pT $/sqrt{Hz}$ for an alternating-current magnetic field near 14 MHz. Based on the principle demonstrated here, this unprecedented sensitivity combined with spatial resolution in the nanometer range and tunability from direct-current to the gigahertz range could be used for magnetic imaging in as of yet inaccessible parameter regimes.
We describe the construction of a fast field cycling device capable of sweeping a 4-order-of-magnitude range of magnetic fields, from ~1mT to 7T, in under 700ms. Central to this system is a high-speed sample shuttling mechanism between a superconducting magnet and a magnetic shield, with the capability to access arbitrary fields in between with high resolution. Our instrument serves as a versatile platform to harness the inherent dichotomy of spin dynamics on offer at low and high fields - in particular, the low anisotropy, fast spin manipulation, and rapid entanglement growth at low field as well as the long spin lifetimes, spin specific control, and efficient inductive measurement possible at high fields. Exploiting these complementary capabilities in a single device open up applications in a host of problems in quantum control, sensing, and information storage, besides in nuclear hypepolarization, relaxometry and imaging. In particular, in this paper, we focus on the ability of the device to enable low-field hyperpolarization of 13C nuclei in diamond via optically pumped electronic spins associated with Nitrogen Vacancy (NV) defect centers.