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Jiangchuan You

Publications and source records attributed to Jiangchuan You.

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Zeno and Anti-Zeno Effects in Dark-State Dynamics Under Thermal Dephasing: A Numerical Study

The quantum Zeno and anti-Zeno effects describe how frequent measurements can either suppress or accelerate quantum dynamics. While extensively studied in various platforms, their manifestation in dark-state dynamics remains largely unexplored. Here we investigate the stability of dark states in a cavity quantum electrodynamics (QED) system consisting of two atoms coupled to a single-mode cavity, subject to thermal dephasing that models continuous quantum non-demolition monitoring. Using the Tavis--Cummings model within a Lindblad master equation framework, we perform numerical simulations to investigate how measurement-induced dephasing affects dark-state retention and stabilization time. Through systematic numerical scans, we identify distinct parameter regimes corresponding to Zeno and anti-Zeno behavior: at low dephasing intensities, increasing the measurement strength accelerates the loss of dark-state coherence (anti-Zeno regime), while at higher intensities, it slows down the dynamics and partially recovers dark-state weight (Zeno regime). The transition between these regimes is controlled by the dephasing rates, the cavity photon exchange, and the asymmetry in atom--field couplings. We show that even under strong dephasing, a finite dark-state component persists, demonstrating remarkable robustness. Our results provide insights into the interplay between measurement back-action and decoherence in open quantum systems, with implications for quantum control and information storage.

quant-ph

Simulating and investigating various dynamic aspects of the $\rm{H}_2\rm{O}$-related hydrogen bond model

A basic model of hydrogen bonds related to $\rm{H}_2\rm{O}$, which is adapted from the Jaynes--Cummings model, is suggested, and its different dynamic features are studied theoretically. In this model, the making and breaking of hydrogen bonds happen alongside the creation and destruction of phonons in the surrounding medium. A number of simplifying assumptions about the dynamics of the molecules involved are used. The rotating wave approximation is applied under consideration of the strong-coupling condition. Dissipative dynamics under the Markovian approximation is obtained through solving the quantum master equation -- Lindbladian. We obtain the probabilities of reaction channels involving hydrogen bonds based on the parameters of the external environment. Differences between unitary and dissipative evolutions are discussed. Consideration is given to the effects of all kinds of potential interactions and dissipation on evolution. Consideration is also given to the reverse processes (inflows) of dissipation. The results show that the magnitude changes of the interactions and dissipation have a slight effect on the formation of hydrogen bonds, but the variation of the inflows significantly affects the formation of hydrogen bonds. According to the findings, the dynamics of the $\rm{H}_2\rm{O}$-related hydrogen bond model can be controlled by selectively choosing system parameters. The results will be used as a basis to extend the research to more complex chemical and biological models in the future.

quant-ph