Quantum repeaters based on individual electron spins and nuclear-spin-ensemble memories in quantum dots

Inspired by recent developments in the control and manipulation of quantum dot nuclear spins, which allow for the transfer of an electron spin state to the surrounding nuclear-spin ensemble for storage, we propose a quantum repeater scheme that combines individual quantum dot electron spins and nuclear-spin ensembles, which serve as spin-photon interfaces and quantum memories respectively. We consider the use of low-strain quantum dots embedded in high-cooperativity optical microcavities. Quantum dot nuclear-spin ensembles allow for the long-term storage of entangled states, and heralded entanglement swapping is performed using cavity-assisted gates. We highlight the advances in quantum dot technologies required to realize our quantum repeater scheme which promises the establishment of high-fidelity entanglement over long distances with a distribution rate exceeding that of the direct transmission of photons.

Direct observation of chaotic resonances in optical microcavities

Optical microcavities play a significant role in the study of classical and quantum chaos. To date, most experimental explorations of their internal wave dynamics have focused on the properties of their inputs and outputs, without directly interrogating the dynamics and the associated mode patterns inside. As a result, this key information is rarely retrieved with certainty, which significantly restricts the verification and understanding of the actual chaotic motion. Here we demonstrate a simple and robust approach to directly and rapidly map the internal mode patterns in chaotic microcavities. By introducing a local index perturbation through a pump laser, we report a spectral response of optical microcavities that is proportional to the internal field distribution. With this technique, chaotic modes with staggered mode spacings can be distinguished. Consequently, a complete chaos assisted tunneling (CAT) and its time-reversed process are experimentally verified in the optical domain with unprecedented certainty.

Operando monitoring transition dynamics of responsive polymer using optofluidic microcavities

Optical microcavities have become an attractive platform for precision measurement with merits of ultrahigh sensitivity, miniature footprint and fast response. Despite the achievements of ultrasensitive detection, optical microcavities still face significant challenges in the measurement of biochemical and physical processes with complex dynamics, especially when multiple effects are present. Here we demonstrate operando monitoring of the transition dynamics of a phase-change material via a self-referencing optofluidic microcavity. We use a pair of cavity modes to precisely decouple the refractive index and temperature information of the analyte during the phase-transition process. Through real-time measurements, we reveal the detailed hysteresis behaviors of refractive index during the irreversible phase transitions between hydrophilic and hydrophobic states. We further extract the phase-transition threshold by analyzing the steady-state refractive index change at various power levels. Our technology could be further extended to other materials and provide great opportunities for exploring on-demand dynamic biochemical processes.

Selective Crystallization via Vibrational Strong Coupling

The coupling of (photo)chemical processes to optical cavity vacuum fields is an emerging method for modulating molecular and material properties. Recent reports have shown that strong coupling of the vibrational modes of solvents to cavity vacuum fields can influence the chemical reaction kinetics of dissolved solutes. This suggests that vibrational strong coupling might also effect other important solution-based processes, such as crystallization from solution. Here we test this hither-to unexplored notion, investigating pseudopolymorphism in the crystallization from water of ZIF metal-organic frameworks inside optical microcavities. We find that ZIF-8 crystals are selectively obtained from solution inside optical microcavities, where the OH stretching vibration of water is strongly coupled to cavity vacuum fields, whereas mixtures of ZIF-8 and ZIF-L are obtained otherwise. This work suggests that cavity vacuum fields might become a tool for materials synthesis, biasing molecular self-assembly and driving macroscopic material outcomes.