Yong Wan

High-precision optical phase stabilization in quantum networks is fundamentally constrained by the strict photon-flux and duty-cycle limits required to avoid disturbing fragile quantum states. This challenge becomes especially critical when coordinating multiple independent light sources for multi-step quantum protocols. Here, we develop an integrated phase-stabilization framework that incorporates a Bayesian phase estimator to optimally extract information from sparse single-photon detection events. This approach outperforms conventional maximum-likelihood estimation and achieves the shot-noise limit under minimal photon flux. The framework enables real-time correction of combined phase noise from both nodal lasers and transmission fibers, facilitating a two-step excitation protocol for heralded entanglement generation between separate trapped-ion nodes via single-photon interference. Operating with a detected photon rate of approximately 1 MHz and a duty cycle less than or equal to 6.5%, the system maintains interferometric visibility greater than 97% over fiber links of 10 km and 100 km. This phase control yields deterministic ion-ion entanglement with parity contrast exceeding 85% at both distances, enabling device-independent quantum key distribution. Moreover, the resulting memory-memory entanglement at 10 km survives beyond the average time required to establish it -- a fundamental requirement for quantum repeaters. This work establishes a robust and scalable foundation for practical long-distance quantum networks.

Quantum networks, integrating quantum communication, quantum metrology, and distributed quantum computing, could provide secure and efficient information transfer, high-resolution sensing, and an exponential speed-up in information processing. Deterministic entanglement distribution over long distances is a prerequisite for scalable quantum networks, enabling the utilization of device-independent quantum key distribution (DI-QKD) and quantum teleportation to achieve secure and efficient information transfer. However, the exponential photon loss in optical fibres prohibits efficient and deterministic entanglement distribution. Quantum repeaters, incorporating entanglement swapping and entanglement purification with quantum memories, offer the most promising means to overcome this limitation in fibre-based quantum networks. Despite numerous pioneering efforts toward realizing quantum repeaters, a critical bottleneck remains, as remote memory-memory entanglement suffers from decoherence more rapidly than it can be established and purified over long distances. We overcome this by developing long-lived trapped-ion memories, an efficient telecom interface, and a high-visibility single-photon entanglement protocol. This allows us to establish and maintain memory-memory entanglement over a 10 km fibre within the average entanglement establishment time for the same distance. As a direct application, we demonstrate metropolitan-scale DI-QKD, distilling 1,917 secret keys out of 4.05*10^5 Bell pairs over 10 km. We further report a positive key rate over 101 km in the asymptotic limit, extending the achievable distance by more than two orders of magnitude. Our work provides a critical building block for quantum repeaters and marks an important step toward scalable quantum networks.

Large-scale quantum computers will require quantum gate operations between widely separated qubits. A method for implementing such operations, known as quantum gate teleportation (QGT), requires only local operations, classical communication, and shared entanglement. We demonstrate QGT in a scalable architecture by deterministically teleporting a controlled-NOT (CNOT) gate between two qubits in spatially separated locations in an ion trap. The entanglement fidelity of our teleported CNOT is in the interval [0.845, 0.872] at the 95% confidence level. The implementation combines ion shuttling with individually-addressed single-qubit rotations and detections, same- and mixedspecies two-qubit gates, and real-time conditional operations, thereby demonstrating essential tools for scaling trapped-ion quantum computers combined in a single device.

Efficient preparation and detection of the motional state of trapped ions is important in many experiments ranging from quantum computation to precision spectroscopy. We investigate the stimulated Raman adiabatic passage (STIRAP) technique for the manipulation of motional states in a trapped ion system. The presented technique uses a Raman coupling between two hyperfine ground states in $^{25}$Mg$^+$, implemented with delayed pulses, which removes a single phonon independent of the initial motional state. We show that for a thermal state the STIRAP population transfer is more efficient than a stimulated Raman Rabi pulse on a motional sideband. In contrast to previous implementations, a large detuning of more than 200 times the natural linewidth of the transition is used. This approach renders STIRAP suitable for atoms in which resonant laser fields would populate fluorescing excited states and thus impede the STIRAP process. We use the technique to measure the wavefunction overlap of excited motional states with the motional ground state. This is an important application for photon recoil spectroscopy and other force sensing applications that utilize the high sensitivity of the motional state of trapped ions to external fields. Furthermore, a determination of the ground state population enables a simple measurement of the ion's temperature.

Laser spectroscopy of cold and trapped molecular ions is a powerful tool for fundamental physics, including the determination of fundamental constants, the laboratory test for their possible variation, and the search for a possible electric dipole moment of the electron. Optical clocks based on molecular ions sensitive to some of these effects are expected to achieve uncertainties approaching the $10^{-18}$ level. While the complexity of molecular structure facilitates these applications, the absence of cycling transitions poses a challenge for direct laser cooling, quantum state control, and detection. Previously employed state detection techniques based on photo-dissociation or chemical reactions are destructive and therefore inefficient. Here we experimentally demonstrate non-destructive state detection of a single trapped molecular ion through its strong Coulomb coupling to a well-controlled co-trapped atomic ion. An algorithm based on a state-dependent optical dipole force(ODF) changes the internal state of the atom conditioned on the internal state of the molecule. We show that individual states in the molecule can be distinguished by their coupling strength to the ODF and observe black-body radiation-induced quantum jumps between rotational states. Using the detuning dependence of the state detection signal, we implement a variant of quantum logic spectroscopy and improve upon a previous measurement of the $\mathrm{X}^1Σ^+(J=1)\rightarrow\mathrm{A}^1Σ^+(J=0)$ transition in MgH, finding a frequency of 1067.74752(53)THz. We estimate that non-destructive state detection with near 100% efficiency could take less than 10 ms. The technique we demonstrate is applicable to a wide range of molecular ions, enabling further applications in state-controlled quantum chemistry and spectroscopic investigations of molecules serving as probes for interstellar clouds.

We demonstrate an efficient high-precision optical spectroscopy technique for single trapped ions with non-closed transitions. In a double-shelving technique, the absorption of a single photon is first amplified to several phonons of a normal motional mode shared with a co-trapped cooling ion of a different species, before being further amplified to thousands of fluorescence photons emitted by the cooling ion using the standard electron shelving technique. We employ this extension of the photon recoil spectroscopy technique to perform the first high precision absolute frequency measurement of the $^{2}$D$_{3/2}$ $\rightarrow$ $^{2}$P$_{1/2}$ transition in $^{40}$Ca$^{+}$, resulting in a transition frequency of $f=346\, 000\, 234\, 867(96)$ kHz. Furthermore, we determine the isotope shift of this transition and the $^{2}$S$_{1/2}$ $\rightarrow$ $^{2}$P$_{1/2}$ transition for $^{42}$Ca$^{+}$, $^{44}$Ca$^{+}$ and $^{48}$Ca$^{+}$ ions relative to $^{40}$Ca$^{+}$ with an accuracy below 100 kHz. Improved field and mass shift constants of these transitions as well as changes in mean square nuclear charge radii are extracted from this high resolution data.

Precision spectroscopy of atomic and molecular ions offers a window to new physics, but is typically limited to species with a cycling transition for laser cooling and detection. Quantum logic spectroscopy has overcome this limitation for species with long-lived excited states. Here, we extend quantum logic spectroscopy to fast, dipole-allowed transitions and apply it to perform an absolute frequency measurement. We detect the absorption of photons by the spectroscopically investigated ion through the photon recoil imparted on a co-trapped ion of a different species, on which we can perform efficient quantum logic detection techniques. This amplifies the recoil signal from a few absorbed photons to thousands of fluorescence photons. We resolve the line center of a dipole-allowed transition in 40Ca+ to 1/300 of its observed linewidth, rendering this measurement one of the most accurate of a broad transition. The simplicity and versatility of this approach enables spectroscopy of many previously inaccessible species.

Protocols used in quantum information and precision spectroscopy rely on efficient internal quantum state discrimination. With a single ion in a linear Paul trap, we implement a novel detection method which utilizes correlations between two detection events with an intermediate spin-flip. The technique is experimentally characterized as more robust against fluctuations in detection laser power compared to conventionally implemented methods. Furthermore, systematic detection errors which limit the Rabi oscillation contrast in conventional methods are overcome.

We present a single solid-state laser system to cool, coherently manipulate and detect $^{25}$Mg$^+$ ions. Coherent manipulation is accomplished by coupling two hyperfine ground state levels using a pair of far-detuned Raman laser beams. Resonant light for Doppler cooling and detection is derived from the same laser source by means of an electro-optic modulator, generating a sideband which is resonant with the atomic transition. We demonstrate ground-state cooling of one of the vibrational modes of the ion in the trap using resolved-sideband cooling. The cooling performance is studied and discussed by observing the temporal evolution of Raman-stimulated sideband transitions. The setup is a major simplification over existing state-of-the-art systems, typically involving up to three separate laser sources.