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C. W. Chou

Publications and source records attributed to C. W. Chou.

At least 19 recordsLinked to original sources

Lifetime-Limited Interrogation of Two Independent ${}^{27}\textrm{Al}^{+}$ Clocks Using Correlation Spectroscopy

Laser decoherence limits the stability of optical clocks by broadening the observable resonance linewidths and adding noise during the dead time between clock probes. Correlation spectroscopy avoids these limitations by measuring correlated atomic transitions between two ensembles, which provides a frequency difference measurement independent of laser noise. Here, we apply this technique to perform stability measurements between two independent clocks based on the $^1S_0\leftrightarrow{}^3P_0$ transition in $^{27}$Al$^+$. By stabilizing the dominant sources of differential phase noise between the two clocks, we observe coherence between them during synchronous Ramsey interrogations as long as 8 s at a frequency of $1.12\times10^{15}$ Hz. The observed contrast in the correlation spectroscopy signal is consistent with the 20.6 s $^3P_0$ state lifetime and supports a measurement instability of $(1.8\pm0.5)\times 10^{-16}/\sqrt{τ/\textrm{s}}$ for averaging periods longer than the probe duration when deadtime is negligible.

physics.atom-ph

Systematic uncertainty due to background-gas collisions in trapped-ion optical clocks

We describe a framework for calculating the frequency shift and uncertainty of trapped-ion optical atomic clocks caused by background-gas collisions, and apply this framework to an $^{27}$Al$^+$ clock to enable a total fractional systematic uncertainty below $10^{-18}$. For this clock, with 38(19) nPa of room temperature H$_2$ background gas, we find that collisional heating generates a non-thermal distribution of motional states with a mean time-dilation shift of order $10^{-16}$ at the end of a 150 ms probe, which is not detected by sideband thermometry energy measurements. However, the contribution of collisional heating to the spectroscopy signal is highly suppressed and we calculate the BGC shift to be $-0.6(2.4)\times 10^{-19}$, where the shift is due to collisional heating time-dilation and the uncertainty is dominated by the worst case $\pm π/2$ bound used for collisional phase shift of the $^{27}$Al$^+$ superposition state. We experimentally validate the framework and determine the background-gas pressure in situ using measurements of the rate of collisions that cause reordering of mixed-species ion pairs.

physics.atom-ph

Measurements of $^{27}$Al$^{+}$ and $^{25}$Mg$^{+}$ magnetic constants for improved ion clock accuracy

We have measured the quadratic Zeeman coefficient for the ${^{1}S_{0} \leftrightarrow {^{3}P_{0}}}$ optical clock transition in $^{27}$Al$^{+}$, $C_{2}=-71.944(24)$~MHz/T$^{2}$, and the unperturbed hyperfine splitting of the $^{25}$Mg$^{+}$ $^{2}S_{1/2}$ ground electronic state, $ΔW / h = 1~788~762~752.85(13)$~Hz, with improved uncertainties. Both constants are relevant to the evaluation of the $^{27}$Al$^{+}$ quantum-logic clock systematic uncertainty. The measurement of $C_{2}$ is in agreement with a previous measurement and a new calculation at the $1~σ$ level. The measurement of $ΔW$ is in good agreement with a recent measurement and differs from a previously published result by approximately $2σ$. With the improved value for $ΔW$, we deduce an improved value for the nuclear-to-electronic g-factor ratio $g_{I}/g_{J} = 9.299 ~308 ~313(60) \times 10^{-5}$ and the nuclear g-factor for the $^{25}$Mg nucleus $g_{I} = 1.861 ~957 ~82(28) \times 10^{-4}$. Using the values of $C_{2}$ and $ΔW$ presented here, we derive a quadratic Zeeman shift of the $^{27}$Al$^{+}$ quantum-logic clock of $Δν/ ν= -(9241.8 \pm 3.7) \times 10^{-19}$, for a bias magnetic field of $B \approx 0.12$~mT.

physics.atom-ph

An $^{27}$Al$^{+}$ quantum-logic clock with systematic uncertainty below $10^{-18}$

We describe an optical atomic clock based on quantum-logic spectroscopy of the $^1$S$_0$ $\leftrightarrow$ $^3$P$_0$ transition in $^{27}$Al$^{+}$ with a systematic uncertainty of ${9.4 \times 10^{-19}}$ and a frequency stability of ${1.2\times10^{-15}/\sqrtτ}$. A $^{25}$Mg$^{+}$ ion is simultaneously trapped with the $^{27}$Al$^{+}$ ion and used for sympathetic cooling and state readout. Improvements in a new trap have led to reduced secular motion heating, compared to previous $^{27}$Al$^{+}$ clocks, enabling clock operation with ion secular motion near the three-dimensional ground state. Operating the clock with a lower trap drive frequency has reduced excess micromotion compared to previous $^{27}$Al$^{+}$ clocks. Both of these improvements have led to a reduced time-dilation shift uncertainty. Other systematic uncertainties including those due to blackbody radiation and the second-order Zeeman effect have also been reduced.

physics.atom-ph

Sympathetic ground state cooling and time-dilation shifts in an $^{27}\text{Al}^+$ optical clock

We report on Raman sideband cooling of ${^{25}\text{Mg}^+}$ to sympathetically cool the secular modes of motion in a $^{25}\text{Mg}^+$-$^{27}\!\text{Al}^+$ two-ion pair to near the three-dimensional (3D) ground state. The evolution of the Fock-state distribution during the cooling process is studied using a rate-equation simulation, and various heating sources that limit the efficiency of 3D sideband cooling in our system are discussed. We characterize the residual energy and heating rates of all of the secular modes of motion and estimate a secular motion time-dilation shift of ${-(1.9 \pm 0.1)\times 10^{-18}}$ for an ${^{27}\text{Al}^+}$ clock at a typical clock probe duration of $150$ ms. This is a 50-fold reduction in the secular motion time-dilation shift uncertainty in comparison with previous ${^{27}\text{Al}^+}$ clocks.

physics.atom-ph

Two-Atom Rydberg Blockade using Direct 6S to nP Excitation

We explore a single-photon approach to Rydberg state excitation and Rydberg blockade. Using detailed theoretical models, we show the feasibility of direct excitation, predict the effect of background electric fields, and calculate the required interatomic distance to observe Rydberg blockade. We then measure and control the electric field environment to enable coherent control of Rydberg states. With this coherent control, we demonstrate Rydberg blockade of two atoms separated by 6.6(3) μm. When compared with the more common two-photon excitation method, this single-photon approach is advantageous because it eliminates channels for decoherence through photon scattering and AC Stark shifts from the intermediate state while moderately increasing Doppler sensitivity.

physics.atom-ph

Trapped-Ion State Detection through Coherent Motion

We demonstrate a general method for state detection of trapped ions that can be applied to a large class of atomic and molecular species. We couple a "spectroscopy" ion (Al+) to a "control" ion (Mg+) in the same trap and perform state detection through off-resonant laser excitation of the spectroscopy ion that induces coherent motion. The motional amplitude, dependent on the spectroscopy ion state, is measured either by time-resolved photon counting, or by resolved sideband excitations on the control ion. The first method provides a simplified way to distinguish "clock" states in Al+, which avoids ground state cooling and sideband transitions. The second method reduces spontaneous emission and optical pumping on the spectroscopy ion, which we demonstrate by nondestructively distinguishing Zeeman sublevels in the 1S0 ground state of Al+.

quant-ph

Quantum coherence between two atoms beyond Q=10^15

We place two atoms in quantum superposition states and observe coherent phase evolution for 3.4x10^15 cycles. Correlation signals from the two atoms yield information about their relative phase even after the probe radiation has decohered. This technique was applied to a frequency comparison of two Al+ ions, where a fractional uncertainty of 3.7+1.0-0.8x10^-16/\sqrt{τ/s} was observed. Two measures of the Q-factor are reported: The Q-factor derived from quantum coherence is 3.4+2.4-1.1x10^16, and the spectroscopic Q-factor for a Ramsey time of 3 s is 6.7x10^15. As part of this experiment, we demonstrate a method to detect the individual quantum states of two Al+ ions in a Mg+-Al+-Al+ linear ion chain without spatially resolving the ions.

quant-ph

Preparation of Dicke States in an Ion Chain

We have investigated theoretically and experimentally a method for preparing Dicke states in trapped atomic ions. We consider a linear chain of $N$ ion qubits that is prepared in a particular Fock state of motion, $|m>$. The $m$ phonons are removed by applying a laser pulse globally to the $N$ qubits, and converting the motional excitation to $m$ flipped spins. The global nature of this pulse ensures that the $m$ flipped spins are shared by all the target ions in a state that is a close approximation to the Dicke state $\D{N}{m}$. We calculate numerically the fidelity limits of the protocol and find small deviations from the ideal state for $m = 1$ and $m = 2$. We have demonstrated the basic features of this protocol by preparing the state $\D{2}{1}$ in two $^{25}$Mg$^+$ target ions trapped simultaneously with an $^{27}$Al$^+$ ancillary ion.

quant-ph

Heralded Entanglement between Atomic Ensembles: Preparation, Decoherence, and Scaling

Heralded entanglement between collective excitations in two atomic ensembles is probabilistically generated, stored, and converted to single photon fields. By way of the concurrence, quantitative characterizations are reported for the scaling behavior of entanglement with excitation probability and for the temporal dynamics of various correlations resulting in the decay of entanglement. A lower bound of the concurrence for the collective atomic state of 0.9\pm 0.3 is inferred. The decay of entanglement as a function of storage time is also observed, and related to the local dynamics.

quant-ph

Towards experimental entanglement connection with atomic ensembles in the single excitation regime

We present a protocol for performing entanglement connection between pairs of atomic ensembles in the single excitation regime. Two pairs are prepared in an asynchronous fashion and then connected via a Bell measurement. The resulting state of the two remaining ensembles is mapped to photonic modes and a reduced density matrix is then reconstructed. Our observations confirm for the first time the creation of coherence between atomic systems that never interacted, a first step towards entanglement connection, a critical requirement for quantum networking and long distance quantum communications.

quant-ph

Conditional control of the quantum states of remote atomic memories for quantum networking

Quantum networks hold the promise for revolutionary advances in information processing with quantum resources distributed over remote locations via quantum-repeater architectures. Quantum networks are composed of nodes for storing and processing quantum states, and of channels for transmitting states between them. The scalability of such networks relies critically on the ability to perform conditional operations on states stored in separated quantum memories. Here we report the first implementation of such conditional control of two atomic memories, located in distinct apparatuses, which results in a 28-fold increase of the probability of simultaneously obtaining a pair of single photons, relative to the case without conditional control. As a first application, we demonstrate a high degree of indistinguishability for remotely generated single photons by the observation of destructive interference of their wavepackets. Our results demonstrate experimentally a basic principle for enabling scalable quantum networks, with applications as well to linear optics quantum computation.

quant-ph

Direct measurement of decoherence for entanglement between a photon and stored atomic excitation

Violations of a Bell inequality are reported for an experiment where one of two entangled qubits is stored in a collective atomic memory for a user-defined time delay. The atomic qubit is found to preserve the violation of a Bell inequality for storage times up to 21 microseconds, 700 times longer than the duration of the excitation pulse that creates the entanglement. To address the question of the security of entanglement-based cryptography implemented with this system, an investigation of the Bell violation as a function of the cross-correlation between the generated nonclassical fields is reported, with saturation of the violation close to the maximum value allowed by quantum mechanics.

quant-ph

Measurement-Induced Entanglement for Excitation Stored in Remote Atomic Ensembles

A critical requirement for diverse applications in Quantum Information Science is the capability to disseminate quantum resources over complex quantum networks. For example, the coherent distribution of entangled quantum states together with quantum memory to store these states can enable scalable architectures for quantum computation, communication, and metrology. As a significant step toward such possibilities, here we report observations of entanglement between two atomic ensembles located in distinct apparatuses on different tables. Quantum interference in the detection of a photon emitted by one of the samples projects the otherwise independent ensembles into an entangled state with one joint excitation stored remotely in 10^5 atoms at each site. After a programmable delay, we confirm entanglement by mapping the state of the atoms to optical fields and by measuring mutual coherences and photon statistics for these fields. We thereby determine a quantitative lower bound for the entanglement of the joint state of the ensembles. Our observations provide a new capability for the distribution and storage of entangled quantum states, including for scalable quantum communication networks .

quant-ph

Control of decoherence in the generation of photon pairs from atomic ensembles

We report an investigation to establish the physical mechanisms responsible for decoherence in the generation of photon pairs from atomic ensembles, via the protocol of Duan et. al for long distance quantum communication [Nature (London) 414, 413 (2001)] and present the experimental techniques necessary to properly control the process. We develop a theory to model in detail the decoherence process in experiments with magneto-optical traps. The inhomogeneous broadening of the ground state by the trap magnetic field is identified as the principal mechanism for decoherence. In conjunction with our theoretical analysis, we report a series of measurements to characterize and control the coherence time in our experimental setup. We use copropagating stimulated Raman spectroscopy to access directly the ground state energy distribution of the ensemble. These spectroscopic measurements allow us to switch off the trap magnetic field in a controlled way, optimizing the repetition rate for single-photon measurements. With the magnetic field off, we then measure nonclassical correlations for pairs of photons generated by the ensemble as a function of the storage time of the single collective atomic excitation. We report coherence times longer than 10 microseconds, corresponding to an increase of two orders of magnitude compared to previous results in cold ensembles. The coherence time is now two orders of magnitude longer than the duration of the excitation pulses. The comparison between these experimental results and the theory shows good agreement. Finally, we employ our theory to devise ways to improve the experiment by optical pumping to specific initial states.

quant-ph

Temporal Dynamics of Photon Pairs Generated by an Atomic Ensemble

The time dependence of nonclassical correlations is investigated for two fields (1,2) generated by an ensemble of cold Cesium atoms via the protocol of Duan et al. [Nature Vol. 414, p. 413 (2001)]. The correlation function R(t1,t2) for the ratio of cross to auto-correlations for the (1,2) fields at times (t1,t2) is found to have a maximum value Rmax=292(+-)57, which significantly violates the Cauchy-Schwarz inequality R<=1 for classical fields. Decoherence of quantum correlations is observed over 175 ns, and is described by our model, as is a new scheme to mitigate this effect.

quant-ph

Single-Photon Generation from Stored Excitation in an Atomic Ensemble

Single photons are generated from an ensemble of cold Cs atoms via the protocol of Duan et al. [Nature \textbf{414}, 413 (2001)]. Conditioned upon an initial detection from field 1 at 852 nm, a photon in field 2 at 894 nm is produced in a controlled fashion from excitation stored within the atomic ensemble. The single-quantum character of the field 2 is demonstrated by the violation of a Cauchy-Schwarz inequality, namely $w(1_{2},1_{2}|1_{1})=0.24\pm 0.05\ngeq 1$, where $w(1_{2},1_{2}|1_{1})$ describes detection of two events $(1_{2},1_{2})$ conditioned upon an initial detection $1_{1}$, with $w\to 0$ for single photons.

quant-ph