SearcharxivSearch

arXiv · 2503.05677

Electric-field sensing with driven-dissipative time crystals in room-temperature Rydberg vapor

Abstract

Mode competition in nonequilibrium Rydberg gases enables the exploration of emergent many-body phases. This work leverages this emergent phase for electric field detection at room temperature. Sensitive frequency-resolved electric field measurements at very low-frequencies (VLF) are of central importance in a wide range of applications where deep-penetration is required in communications, navigation and imaging or surveying. The long wavelengths on order of 10-100 km (3-30 kHz) limit the efficiency, sensitivity, and bandwidth of compact classical detectors that are constrained by the Chu limit. Rydberg-atom electrometers are an attractive approach for microwave electric-field sensors but have reduced sensitivity at lower-frequencies. Very recent efforts to advance the standard Rydberg-atoms approach is based on DC electric-field (E-field) Stark shifting and have resulted in sensitivities between 67.9-2.2 uVcm-1Hz-1/2 (0.1-10 kHz) by fine optimization of the DC E-field. A major challenge in these approaches is the need for embedded electrodes or plates due to DC E-field Stark screening effect, which can perturb coupling of VLF signals when injected from external sources. In this article, it is demonstrated that state-of-art sensitivity (~1.6-2.3 uVcm-1Hz-1/2) can instead be achieved using limit-cycle oscillations in driven-dissipative Rydberg atoms by using a magnetic field (B-field) to develop mode-competition between nearby Rydberg states. The mode-competition between nearby Rydberg-states develop an effective transition centered at the oscillation frequency capable of supporting external VLF E-field coupling in the ~10-15kHz regime without the requirement for fine optimization of the B-field magnitude.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Darmindra Arumugam. 2025-03-07. Electric-field sensing with driven-dissipative time crystals in room-temperature Rydberg vapor. https://arxiv.org/abs/2503.05677

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Delay-engineered dynamical phases in a programmable non-Markovian spin oscillator

Non-Markovian dynamics offer a new route towards engineering non-equilibrium matter, where memory and feedback act as programmable resources for controlling order in time. Here we report the realization of a non-Markovian spin oscillator in a hot vapour $^{129}$Xe-Cs co-magnetometer with programmable feedback delay and gain. By tuning these parameters, we observe a hierarchy of dynamical phases, including time-crystalline response, nonlinear bifurcations, and frequency-comb formation. The measured spectra and phase boundaries are captured by linear stability analysis of delayed Bloch equations, revealing these phenomena as different manifestations of the same memory-induced instability structure. These results establish time-delayed feedback as a powerful strategy for controlling non-equilibrium phases, enabling quantum sensing, frequency referencing, and synchronization within a single spin-based platform.

physics.atom-ph

Non-stick vacuum wall collisions with a laser-coolable molecule

Molecular species that are suitable for direct laser cooling are typically considered lost or destroyed if they collide with an ambient temperature vacuum wall. Here, we study surface collisions with aluminum monofluoride (AlF), a laser-coolable molecule that survives this process with unusually high probability. We detect the outgoing AlF molecules from a single wall collision via Doppler-sensitive laser-induced fluorescence spectroscopy, using incoming supersonic (pulsed) and thermochemical (continuous) molecular beams. The angular, velocity and rovibrational level distributions of the outgoing molecules show near-complete thermalisation to the wall in a single collision event. We determine an upper limit to the surface residence time of about 5$~\mu$s, and by monitoring the decay in density of pulses of molecules loaded into a small storage volume, we deduce the surface sticking probability for different materials. For a siloxane-coated metallic surface, the sticking probability of AlF is about 0.015, allowing us to accumulate molecules from the thermochemical source into an ambient temperature storage vessel at densities near $10^{8}~$cm$^{-3}$. This provides a route to compact, portable traps for neutral molecules.

physics.atom-ph

Kinetic modeling of molecular beam formation in a cryogenic buffer-gas cell

Cryogenic buffer-gas cells are widely used to produce cold molecular beams, but the microscopic dynamics governing beam formation remain challenging to model. Here we present fully kinetic simulations of a cryogenic buffer-gas cell using the Direct Simulation Monte Carlo method implemented in the PICLas framework, treating the buffer gas and ablated molecules within a single unified model. We capture characteristic features of cryogenic buffer-gas sources, including plume cooling, directed transport toward the aperture, and the formation of a slow molecular beam, while also resolving energy transfer from the hot ablation plume to the helium buffer gas that is inaccessible to existing approaches relying on the background-gas approximation. Our results demonstrate that fully kinetic simulations can provide detailed insights into buffer-gas cell dynamics and open a route toward a systematic optimization of such sources.

physics.atom-ph