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Discrete Time Crystal Phase as a Resource for Quantum Enhanced Sensing

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arxiv 2405.00328 v4 pith:RCJW5TLL submitted 2024-05-01 quant-ph cond-mat.str-el

classification quant-phcond-mat.str-el
keywords phasetimecrystaldiscretesystemcharacterizecouplingdriving
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Discrete time crystals are a special phase of matter in which time translational symmetry is broken through a periodic driving pulse. Here, we first propose and characterize an effective mechanism to generate a stable discrete time crystal phase in a disorder-free many-body system with indefinite persistent oscillations even in finite-size systems. Then we explore the sensing capability of this system to measure the spin exchange coupling. The results show strong quantum-enhanced sensitivity throughout the time crystal phase. As the spin exchange coupling varies, the system goes through a sharp phase transition and enters a non-time crystal phase in which the performance of the probe considerably decreases. We characterize this phase transition as a second-order type and determine its critical properties through a comprehensive finite-size scaling analysis. The performance is independent of the initial states and may even benefit from imperfections in the driving pulse. A simple set of projective measurements can capture the quantum-enhanced sensitivity.

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Cited by 2 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. The Floquet central spin model: A platform to realize eternal time crystals, entanglement steering, and multiparameter metrology

    quant-ph 2025-01 reject novelty 6.0 of 10

    Eternal discrete time crystals, including higher-order ones with periods of 12T or 24T, can be realized in the driven central spin model at specific interaction strengths, and these phases can generate Bell-cat states...

  2. Role of long-range interaction in critical quantum metrology

    quant-ph 2025-01 conditional novelty 6.0 of 10

    In a long-range Kitaev chain, the quantum Fisher information for estimating the chemical potential retains Heisenberg scaling with system size squared and is enhanced by reducing the interaction decay exponent.

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