In recent years, the growing scale of programmable neutral-atom arrays has led to an increasing demand for higher-power Rydberg excitation light. Although pulsed amplifiers deliver higher peak power than continuous-wave lasers, their use for efficient coherent Rydberg excitation of single atoms in arrays has been limited by challenges such as pulse distortion, synchronization with excitation sequences, and spectral linewidth broadening. Here, we address these issues using a fiber-based master-oscillator power-amplifier system. We demonstrate efficient coherent Rydberg excitation of single atoms in a rubidium atom array, achieving performance comparable to continuous-wave methods. This study provides a potentially new technical pathway toward future large-scale quantum simulation and computation with Rydberg atom arrays.
In recent years, the growing scale of programmable neutral-atom arrays has led to an increasing demand for higher-power Rydberg excitation light. Although pulsed amplifiers deliver higher peak power than continuous-wave lasers, their use for efficient coherent Rydberg excitation of single atoms in arrays has been limited by challenges such as pulse distortion, synchronization with excitation sequences, and spectral linewidth broadening. Here, we address these issues using a fiber-based master-oscillator power-amplifier system. We demonstrate efficient coherent Rydberg excitation of single atoms in a rubidium atom array, achieving performance comparable to continuous-wave methods. This study provides a potentially new technical pathway toward future large-scale quantum simulation and computation with Rydberg atom arrays.
The development of highly customized technical devices is a decisive feature of technically complex setups, as frequently observed in quantum experiments. This paper describes the development and realization of an Yb-doped all-fiber amplifier system designed for such a special application, more specifically, an on-demand single-photon source based on four-wave mixing with rubidium Rydberg atoms. The laser is capable of generating bandwidth-limited configurable nanosecond pulses up to peak powers of >100 W and with pulse repetition frequencies (PRF) between 50 Hz and 1 MHz at selectable wavelengths (1008-1024 nm). Especially the amplification of the 1010 nm reference seed at the lower edge of the amplification range for Yb-based fibers is challenging and tends to produce amplified spontaneous emission (ASE) at higher wavelengths. To achieve high ASE suppression, particularly at low pulse repetition frequencies, two acousto-optical modulators (AOM) are utilized both for pulse picking and for temporal filtering. The synchronization between pulse repetition frequency and AOM driver signal allows pulse amplitude fluctuations to be kept below 1%, while ASE is suppressed by at least 85 dB (PRF = 1 MHz) and 65 dB (PRF = 1 kHz).
Atoms in Rydberg states are an important building block for emerging quantum technologies. While excitation to Rydberg orbitals is typically achieved in more than tens of nanoseconds, the physical limit is in fact much faster, at the ten picoseconds level. Here, we tackle such ultrafast Rydberg excitation of a rubidium atom by designing a dedicated pulsed laser system generating 480 nm pulses of 10 ps duration. In particular, we improved upon our previous design by using an injection-seeded optical parametric amplifier (OPA) to obtain a stable pulsed energy, decreasing the fluctuation from 30 to 6%. We then succeeded in ultrafast excitation of Rydberg atoms with excitation probability of ∼90%, not limited anymore by energy fluctuation but rather by the atomic state preparation, addressable in future works. This achievement broadens the range of applications of Rydberg atoms.
Single photon source is a non-classical light field with anti-bunching effect, which has a potential applications in the research of fundamental physics problems, quantum precision measurement, quantum communication, quantum computing, etc. The strong interaction between highly excited Rydberg atoms presents an excitation blockade effect. In a dense Rydberg atomic ensemble, the excitation of more than one Rydberg atom within a blockade volume is suppressed, where the interactions of Rydberg atoms shift the atomic states out of resonance with an excitation laser. We consider here the generation of single photon source by using a four-wave mixing scheme in a room-temperature atomic vapor cell. In a homemade micrometer-sized atomic vapor cell, one-dimensional size is smaller than the radius of Rydberg blockade and the other two-dimensional size is limited by the size of focused laser beam. The blockade radius is on the order of a few micrometers, depending on the Rydberg atom states. An excitation blockade effect can be used to realize single photon source in thermal cesium vapor microcells. The micron cesium-cell is used to spatially localize atomic groups, which results in the atomic decoherence time on the order of microseconds or even nanoseconds. This requires a high-power pulsed laser to prepare the Rydberg atomic state at a nanosecond scale. Four-photon excitation schemes with narrow linewidth lasers are also used experimentally. The cesium-Rydberg state can usually be excited by the lasers with optical wavelengths 852 and 509 nm, respectively. The laser system is well-stabilized so that the detuning is small compared with the spontaneous linewidth of Rydberg state, while the laser power and temporal mode need to be specified for ns-time coherence in thermal cesium vapor microcells. The 852 nm laser can be achieved by modulating the continuous laser beam with the help of an electro-optic intensity modulator (EOIM). While this remains a technical challenge for 509 nm laser with ns-laser pulse. There is no EOIM to generate the ns-laser pulse with high power. We demonstrate a novel generation method of 509 nm laser system. In our experiments, a 1018 nm fiber laser is used to produce a continuous laser with a typical linewidth of ～8 kHz and power of 10 mW. The nanosecond pulse is generated with the help of an electro-optic intensity modulator (EOIM) by modifying the continuous laser beam. The peak power of modulated optical pulse is amplified to 4600 W by using a homemade fiber amplifier. The output beam of 1018 nm is then injected into a periodically poled lithium-niobate (PPLN) to generate the second harmonics laser of 509 nm. The typical peak power of 509 nm reaches 173 W by optimizing PPLN phase matching parameters. The pulse repetition frequency of the 509 nm laser can be continuously tuned in a range of 300 kHz–100 MHz, and the pulse width can be continuously tuned in a range of 1–100 ns. Peak power fluctuation of the pulses is about 1.3%. The power 509 nm laser with optimized pulse parameters can be used to excite the cesium atom with GHz bandwidth. Meanwhile the two seed source lasers is well established experimentally, which allows alternating pulses with a different wavelength. This is an essential capability for realizing a single photon source through four-wave mixing.
Nowadays the long-range dipole-dipole interaction between highly-excited Rydberg atoms at micrometer distance become promising way to establish the atom-atom quantum entanglement and to implement the two-qubit logic gate. For alkali metal atoms, single-photon excitation from the ground state to the desired Rydberg state demands powerful narrow-linewidth ultra-violet (UV) laser, which is very challenging. Maybe just because of this, the studies of single-photon Rydberg excitation of alkali metal atoms are rare. Alternatively people have employed the two-photon or three-photon Rydberg excitation scheme. However, comparing with the single-photon Rydberg excitation, the two-photon or three-photon scheme has following drawbacks: atomic decoherence due to the photon scattering from the lower and upper transitions, and light shift of the involved ground state and Rydberg state due to the lower and upper transition laser beams. Thanks to the efficient laser frequency conversion technology with PPXX material and the well-developed commercial fiber laser as well as fiber amplifier, we have implemented a tunable 318.6-nm UV laser system based on the cavity-enhanced second-harmonic generation following the single-pass sum-frequency generation of 1560.5-nm and 1076.9-nm fiber-amplified lasers. More than 2-Watt output of the 318.6-nm UV laser has been achieved with a typical linewidth of smaller than 10 kHz. Employing the UV laser system we have demonstrated a single-photon Rydberg excitation spectroscopy of cesium (Cs) atoms. Partial Cs atoms can be directly excited from 6S_1/2 ground state to nP_3/2 (n = 70 - 100) Rydberg states, and Rydberg excitation spectra are obtained with transmission enhancement of a probe beam locked to Cs 6S_1/2 (F = 4) - 6P_3/2 (F’ = 5) cycling transition because partial population on the ground state (F = 4) are transferred to Rydberg state. The quantum defect for Cs nP_3/2 (n = 70 -100) Rydberg states is determined experimentally. Further more, the demodulated single-photon Rydberg excitation spectrum is employed to stabilize the UV laser to specific Cs Rydberg transition to improve the laser frequency stability. References: [1] Opt. Express 25 (2017) p.22510; [2] J. Opt. 19 (2017) 045501; [3] J. Opt. Soc. Am. B 33 (2016) p.2020; [4] Opt. Commun. 370 (2016) p.150. Funding: the National Natural Science Foundation of China (61475091).
We present the development of a high-power ultraviolet laser system operating at a wavelength of 325 nm for Rydberg excitation from the 3P2 state of ytterbium. Utilizing a two-stage frequency doubling scheme, we achieved an output power exceeding 800 mW. The system effectively suppresses frequency noise in the MHz range, which is critical for achieving high Rydberg excitation fidelity, through the use of a filtering cavity. Using this system, we demonstrated coherent excitation of the (6s71s)3S1 Rydberg state with a Rabi frequency of 2.13(3) MHz. Combined with our successful manipulations on the 1S0−3P2 transition, this work represents a foundational step toward achieving high-fidelity Rydberg excitation, enabling advancements in quantum simulation and computing with neutral atom arrays.
Abstract Neutral atom arrays are particularly promising for large-scale quantum computing because it is possible to prepare large-scale qubit arrays. An unsolved issue is how to selectively excite one qubit deep in a 3D atomic array to Rydberg states. In this work, we show two methods for this purpose. The first method relies on a well-known result: in a dipole transition between two quantum states driven by two off-resonant fields of equal strength but opposite detunings ±Δ, the transition is characterized by two counter-rotating Rabi frequencies Ω e ± i Δ t (or ± Ω e ± i Δ t if the two fields have a π -phase difference). This pair of detuned fields lead to a time-dependent Rabi frequency 2 Ω cos ( Δ t ) (or 2 i Ω sin ( Δ t ) ), so that a full transition between the two levels is recovered. We show that when the two detuned fields are sent in different directions, one atom in a 3D optical lattice can be selectively addressed for Rydberg excitation, and when its state is restored, the state of any nontarget atoms irradiated in the light path is also restored. Moreover, we find that the Rydberg excitation by this method can significantly suppress the fundamental blockade error of a Rydberg gate, paving the way for a high-fidelity entangling gate with a commonly used quasi-rectangular pulse that is easily obtained by pulse pickers. Along the way, we find a second method for single-site Rydberg addressing in 3D, where a selected target atom can be excited to the Rydberg state while preserving the state of any nontarget atom due to a spin-echo sequence. The capability to selectively address a target atom in 3D atomic arrays for Rydberg excitation makes it possible to design a large-scale neutral-atom information processor based on the Rydberg blockade.