A dissipative time crystal is an emergent phase in driven-dissipative quantum many-body systems, characterized by sustained oscillations that break time-translation symmetry spontaneously. Here, we explore nonequilibrium phase transitions in a dissipative Rydberg system driven by a microwave (MW) field and demonstrate their critical sensitivity to high-precision MW sensing. Distinct dynamical regimes are identified, including monostable, bistable, and oscillatory phases under mean-field coupling. Unlike single-particle detection--where the beating signal decays linearly with MW field strength--the time crystalline phase exhibits high sensitivity to MW perturbations, with rapid, discontinuous frequency switching near the monostable-oscillatory boundary. The abrupt transition is rooted in spontaneous symmetry breaking in time and is fundamentally insensitive to the background noise. On this basis, a minimum detectable MW field strength on the order of 1nV/cm is achieved by leveraging this sensitivity. Our results establish a framework for controlling time crystalline phases with external fields and advance MW sensing through many-body effects.
A dissipative time crystal is an emergent phase in driven-dissipative quantum many-body systems, characterized by sustained oscillations that break time-translation symmetry spontaneously. Here, we explore nonequilibrium phase transitions in a dissipative Rydberg system driven by a microwave (MW) field and demonstrate their critical sensitivity to high-precision MW sensing. Distinct dynamical regimes are identified, including monostable, bistable, and oscillatory phases under mean-field coupling. Unlike single-particle detection--where the beating signal decays linearly with MW field strength--the time crystalline phase exhibits high sensitivity to MW perturbations, with rapid, discontinuous frequency switching near the monostable-oscillatory boundary. The abrupt transition is rooted in spontaneous symmetry breaking in time and is fundamentally insensitive to the background noise. On this basis, a minimum detectable MW field strength on the order of 1nV/cm is achieved by leveraging this sensitivity. Our results establish a framework for controlling time crystalline phases with external fields and advance MW sensing through many-body effects.
The pursuit of unprecedented sensitivity in quantum enhanced metrology has spurred interest in non-equilibrium quantum phases of matter and their symmetry breaking. In particular, criticality-enhanced metrology through time-translation symmetry breaking in many-body systems, a distinct paradigm compared to spatial symmetry breaking, is a field still in its infancy. Here, we have investigated the enhanced sensing at the boundary of a continuous time-crystal (CTC) phase in a driven Rydberg atomic gas. By mapping the full phase diagram, we identify the parameter-dependent phase boundary where the time-translation symmetry is broken. This allows us to use a single setup for measuring multiple parameters, in particular frequency and amplitude of a microwave field. By increasing the microwave field amplitude, we first observe a phase transition from a thermal phase to a CTC phase, followed by a second transition into a distinct CTC state, characterized by a different oscillation frequency. Furthermore, we reveal the precise relationship between the CTC phase boundary and the scanning rate, displaying enhanced precision beyond the Standard Quantum Limit. This work not only provides a promising paradigm rooted in the critical properties of time crystals, but also advances a method for multi-parameter sensing in non-equilibrium quantum phases.
Non-equilibrium Rydberg gases exhibit exotic many-body phases stabilized by the interplay of coherent interactions and dissipation. Strong Rydberg interactions drive sustained limit cycle oscillations, whose robustness, long-range temporal order, and spontaneous time-translation symmetry breaking establish a dissipative time crystal (DTC). Collective self-entrainment in driven ensembles leads to global synchronization and a dominant oscillation frequency. Here, injection locking of a Rydberg DTC is demonstrated using a radio-frequency (RF) electric field that gradually pulls the intrinsic oscillation toward the injected frequency. Above a critical threshold, full synchronization occurs, with the locking bandwidth scaling linearly with RF amplitude. This includes synchronization of higher-order harmonics, revealing entrainment of the system’s nonlinear temporal dynamics. The phenomenon parallels injection locking in classical nonlinear systems, but emerges here in a strongly interacting quantum medium. This approach establishes a new method for stabilizing and controlling time-crystalline temporal order, with applications in precision sensing, quantum metrology, and timekeeping. Non-equilibrium Rydberg gases exhibit unique many-body phases arising from the interplay of coherent interactions and dissipation, yet controlling their temporal order remains challenging. This work demonstrates injection locking of a Rydberg dissipative time crystal using a radio-frequency electric field, achieving full synchronization and revealing dynamical behavior relevant to precision sensing and quantum metrology.
Quantum many-body systems near phase transitions respond collectively to externally applied perturbations. We explore this phenomenon in a laser-driven dissipative Rydberg gas that is tuned to a bistable regime. Here two metastable phases coexist, which feature a low and high density of Rydberg atoms, respectively. The ensuing collective dynamics, which we monitor , is characterized by stochastic collective jumps between these two macroscopically distinct many-body phases. We show that the statistics of these jumps can be controlled using a dual-tone microwave field. In particular, we find that the distribution of jump times develops peaks corresponding to subharmonics of the relative microwave detuning. Our study demonstrates the control of collective statistical properties of dissipative quantum many-body systems without the necessity of fine-tuning or of ultracold temperatures. Such robust many-body phenomena may find technological applications in sensing. Published by the American Physical Society 2024
Non-equilibrium Rydberg gases exhibit exotic many-body phases stabilized by the interplay of coherent interactions and dissipation. Strong Rydberg interactions drive sustained limit cycle oscillations, whose robustness, long-range temporal order, and spontaneous time-translation symmetry breaking establish a dissipative time crystal (DTC). Collective self-entrainment in driven ensembles leads to global synchronization and a dominant oscillation frequency. Here, injection locking of a Rydberg DTC is demonstrated using a radio-frequency (RF) electric field that gradually pulls the intrinsic oscillation toward the injected frequency. Above a critical threshold, full synchronization occurs, with the locking bandwidth scaling linearly with RF amplitude. This includes synchronization of higher-order harmonics, revealing entrainment of the system's nonlinear temporal dynamics. The phenomenon parallels injection locking in classical nonlinear systems, but emerges here in a strongly interacting quantum medium. This approach establishes a new method for stabilizing and controlling time-crystalline temporal order, with applications in precision sensing, quantum metrology, and timekeeping.
Microwave power-to-frequency transduction is demonstrated using the emergent oscillation frequency of a magnetically initiated Rydberg dissipative time crystal (DTC). In a room-temperature 87Rb vapor, a ~14 G magnetic field establishes a self-sustained DTC near 21 kHz, while a near-resonant 8.325 GHz field coupling the 63D3/2 to 64P3/2 manifold continuously shifts the autonomous oscillation frequency. The resulting field-to-frequency transfer function is strongly nonlinear, with a total fundamental-frequency excursion of ~6.7 kHz and peak responsivity approaching 1 kHz/(mV/cm). The nonlinear transition is substantially steeper than a simple quadratic saturation response and is captured by a self-consistent mean-field picture in which microwave-driven Rydberg-population redistribution modifies the collective resonance condition. Higher DTC harmonics preserve the same normalized transfer function while exhibiting approximately linear growth of absolute responsivity with harmonic order. These results establish an intrinsic many-body atomic route to RF amplitude-to-frequency conversion, enabling continuous frequency-domain sensing through an emergent atomic frequency without an externally engineered RF feedback oscillator, repeated optical spectral scans, or resolved Autler Townes splitting.
Continuous time crystals (CTCs) are characterized by sustained oscillations that break the time-translation symmetry. Since the ruling out of equilibrium CTCs by no-go theorems, the emergence of such dynamical phases has been observed in various driven-dissipative quantum platforms. The current understanding of CTCs is mainly based on mean-field theories, which fail to address the problem of whether the continuous time-translation symmetry can be broken in noisy, spatially extended systems absent in all-to-all couplings. Here, we propose a CTC realized in a quantum contact model through self-organized bistability. The CTCs stem from the interplay between collective dissipation induced by the first-order absorbing phase transitions and slow constant driving provided by an incoherent pump. The stability of such oscillatory phases in finite dimensions under the action of intrinsic quantum fluctuations is scrutinized by the functional renormalization group method and numerical simulations. Occurring at the edge of many-body synchronization, the CTC phase exhibits an inherent period and amplitude with a coherence time linearly diverging with system size, thus also constituting a boundary time crystal. Our results serve as a solid route towards self-protected CTCs in strongly interacting open systems. Published by the American Physical Society 2024