Discrete Time Crystals in Noninteracting Dissipative Systems
Gourab Das, Saptarshi Saha, Rangeet Bhattacharyya
TL;DR
This work shows that a robust subharmonic response characteristic of discrete time crystals can emerge in a noninteracting open quantum system when dissipation is engineered to stabilize the dynamics. By pairing environment interaction for a duration $\tau$ with a brief $\theta$-pulse sequence, the authors derive analytical results for $\theta = \pi$ and $\theta = \pi + \delta$, revealing a $2T$-periodic response in the magnetization $M_z$ whose lifetime is set by the dissipative timescales $T_1$ and $T_2$ and is independent of system size. The experimental demonstration using Nuclear Magnetic Resonance in $\mathrm{D}_2\mathrm{O}$ confirms the EDTC phenomenon, showing rigidity under near-perfect pulses and controlled degradation under pulse errors, with the ability to mitigate errors by adjusting $\tau$. The findings establish environment-assisted DTC as a distinct dissipative mechanism for time-crystalline order in open quantum systems, broadening the scope beyond interacting or Floquet-prethermal regimes. Overall, the work highlights a practical route to stabilize DTC behavior via controlled dissipation, independent of initial conditions and system size, with potential implications for robust quantum dynamics in noisy environments.
Abstract
Many-body quantum systems, under suitable conditions, exhibit time-translation symmetry breaking and settle in a discrete time crystalline (DTC) phase -- an out-of-equilibrium quantum phase of matter. The defining feature of DTC is a robust subharmonic response. However, the DTC phase is fragile in the presence of environmental dissipation. Here, we propose and exemplify a DTC phase in a noninteracting system that owes its stability to environmental dissipation. The lifetime of this DTC is independent of initial conditions and the size of the system, though it depends on the frequency of the external driver. We experimentally demonstrate this realization of DTC using Nuclear Magnetic Resonance spectroscopy.
