C. Sanner

Coherent suppression of tensor frequency shifts through magnetic field rotation

R. Lange [1], N. Huntemann [1], C. Sanner [1], H. Shao [1], B. Lipphardt [1], Chr. Tamm [1], E. Peik [1]

Abstract

We introduce a scheme to coherently suppress second-rank tensor frequency shifts in atomic clocks, relying on the continuous rotation of an external magnetic field during the free atomic state evolution in a Ramsey sequence. The method retrieves the unperturbed frequency within a single interrogation cycle and is readily applicable to various atomic clock systems. For the frequency shift due to the electric quadrupole interaction, we experimentally demonstrate suppression by more than two orders of magnitude for the ${}^2S_{1/2} \to {}^2D_{3/2}$ transition of a single trapped ${}^{171}\text{Yb}^+$ ion. The scheme provides particular advantages in the case of the ${}^{171}\text{Yb}^+$ ${}^2S_{1/2} \to {}^2F_{7/2}$ electric octupole (E3) transition. For an improved estimate of the residual quadrupole shift for this transition, we measure the excited state electric quadrupole moments $Θ({}^2D_{3/2}) = 1.95(1)~ea_0^2$ and $Θ({}^2F_{7/2}) = -0.0297(5)~ea_0^2$ with $e$ the elementary charge and $a_0$ the Bohr radius, improving the measurement uncertainties by one order of magnitude.

Single-Ion Atomic Clock with $3\times10^{-18}$ Systematic Uncertainty

N. Huntemann [1], C. Sanner [1], B. Lipphardt [1], Chr. Tamm [1], E. Peik [1]

Abstract

We experimentally investigate an optical frequency standard based on the $^2S_{1/2} (F=0)\to {}^2F_{7/2} (F=3)$ electric octupole (\textit{E}3) transition of a single trapped $^{171}$Yb$^+$ ion. For the spectroscopy of this strongly forbidden transition, we utilize a Ramsey-type excitation scheme that provides immunity to probe-induced frequency shifts. The cancellation of these shifts is controlled by interleaved single-pulse Rabi spectroscopy which reduces the related relative frequency uncertainty to $1.1\times 10^{-18}$. To determine the frequency shift due to thermal radiation emitted by the ion's environment, we measure the static scalar differential polarizability of the \textit{E}3 transition as $0.888(16)\times 10^{-40}$ J m$^2$/V$^2$ and a dynamic correction $η(300~\text{K})=-0.0015(7)$. This reduces the uncertainty due to thermal radiation to $1.8\times 10^{-18}$. The residual motion of the ion yields the largest contribution $(2.1\times 10^{-18})$ to the total systematic relative uncertainty of the clock of $3.2\times 10^{-18}$.