Quantum technologies use entanglement to outperform classical technologies, and often employ strong cooling and isolation to protect entangled entities from decoherence by random interactions. Here we show that the opposite strategy - promoting rando
m interactions - can help generate and preserve entanglement. We use optical quantum non-demolition measurement to produce entanglement in a hot alkali vapor, in a regime dominated by random spin-exchange collisions. We use Bayesian statistics and spin-squeezing inequalities to show that at least $1.52(4)times 10^{13}$ of the $5.32(12) times 10^{13}$ participating atoms enter into singlet-type entangled states, which persist for tens of spin-thermalization times and span thousands of times the nearest-neighbor distance. The results show that high temperatures and strong random interactions need not destroy many-body quantum coherence, that collective measurement can produce very complex entangled states, and that the hot, strongly-interacting media now in use for extreme atomic sensing are well suited for sensing beyond the standard quantum limit.
We study causal waveform estimation (tracking) of time-varying signals in a paradigmatic atomic sensor, an alkali vapor monitored by Faraday rotation probing. We use Kalman filtering, which optimally tracks known linear Gaussian stochastic processes,
to estimate stochastic input signals that we generate by optical pumping. Comparing the known input to the estimates, we confirm the accuracy of the atomic statistical model and the reliability of the Kalman filter, allowing recovery of waveform details far briefer than the sensors intrinsic time resolution. With proper filter choice, we obtain similar benefits when tracking partially-known and non-Gaussian signal processes, as are found in most practical sensing applications. The method evades the trade-off between sensitivity and time resolution in coherent sensing.
We report long-term laser frequency stabilization using only the target laser and a pair of 5 m fiber interferometers, one as a frequency reference and the second as a sensitive thermometer to stabilize the frequency reference. When used to stabilize
a distributed feedback laser at 795 nm, the frequency Allan deviation at 1000 s drops from 5.6*10^{-8} to 6.9*10^{-10}. The performance equals that of an offset lock employing a second, atom-stabilized laser in the temperature control.
We demonstrate an optically pumped $^{87}$Rb magnetometer in a microfabricated vapor cell based on a zero-field dispersive resonance generated by optical modulation of the $^{87}$Rb ground state energy levels. The magnetometer is operated in the spin
-exchange relaxation-free regime where high magnetic field sensitivities can be achieved. This device can be useful in applications requiring array-based magnetometers where radio frequency magnetic fields can induce cross-talk among adjacent sensors or affect the source of the magnetic field being measured.
Optically hyperpolarized $^{129}$Xe gas has become a powerful contrast agent in nuclear magnetic resonance (NMR) spectroscopy and imaging, with applications ranging from studies of the human lung to the targeted detection of biomolecules. Equally att
ractive is its potential use to enhance the sensitivity of microfluidic NMR experiments, in which small sample volumes yield poor sensitivity. Unfortunately, most $^{129}$Xe polarization systems are large and non-portable. Here we present a microfabricated chip that optically polarizes $^{129}$Xe gas. We have achieved $^{129}$Xe polarizations greater than 0.5$%$ at flow rates of several microliters per second, compatible with typical microfluidic applications. We employ in situ optical magnetometry to sensitively detect and characterize the $^{129}$Xe polarization at magnetic fields of 1 $mu$T. We construct the device using standard microfabrication techniques, which will facilitate its integration with existing microfluidic platforms. This device may enable the implementation of highly sensitive $^{129}$Xe NMR in compact, low-cost, portable devices.
