C. W. Chou

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.

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.

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+.

We have constructed an optical clock with a fractional frequency inaccuracy of 8.6e-18, based on quantum logic spectroscopy of an Al+ ion. A simultaneously trapped Mg+ ion serves to sympathetically laser-cool the Al+ ion and detect its quantum state. The frequency of the 1S0->3P0 clock transition is compared to that of a previously constructed Al+ optical clock with a statistical measurement uncertainty of 7.0e-18. The two clocks exhibit a relative stability of 2.8e-15/ sqrt(tau), and a fractional frequency difference of -1.8e-17, consistent with the accuracy limit of the older clock.

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.