arXiv subjects

T. Nordmann

Publications and source records attributed to T. Nordmann.

6 recordsLinked to original sources

arXiv2025

High-accuracy multi-ion spectroscopy with mixed-species Coulomb crystals

Multi-ion optical clocks offer the possibility of overcoming the low signal-to-noise ratio of single-ion clocks, while still providing low systematic uncertainties. We present simultaneous spectroscopy of up to four ${}^{115}$In${}^+$ clock ions in a linear Coulomb crystal, sympathetically cooled with ${}^{172}$Yb${}^+$ ions. In first clock comparisons, we see agreement below $1\times10^{-17}$ with results obtained using a single In${}^+$ ion, for which we have evaluated the systematic uncertainty to be $2.5\times10^{-18}$. Operation with four clock ions reduces the instability from $1.6\times10^{-15}/\sqrt{t/(1\;\mathrm{s})}$ to $9.2\times10^{-16}/\sqrt{t/(1\;\mathrm{s})}$. We derive a model for decay-related dead time during state preparation, which matches the observed scaling of instability with clock ion number $N$, and indicates that $1/\sqrt{N}$ scaling can be achieved with the addition of a repump laser.

physics.atom-ph↗

arXiv2024

$^{115}$In$^+$-$^{172}$Yb$^+$ Coulomb crystal clock with $2.5\times10^{-18}$ systematic uncertainty

We present a scalable mixed-species Coulomb crystal clock based on the $^1S_0$ $\leftrightarrow$ $^3P_0$ transition in $^{115}$In$^+$. $^{172}$Yb$^+$ ions are co-trapped and used for sympathetic cooling. Reproducible interrogation conditions for mixed-species Coulomb crystals are ensured by a conditional preparation sequence with permutation control. We demonstrate clock operation with a 1In$^+$-3Yb$^+$ crystal, achieving a relative systematic uncertainty of $2.5\times10^{-18}$ and a relative frequency instability of $1.6\times10^{-15}/\sqrt{\tau/1\;\mathrm{s}}$. We report on absolute frequency measurements with an uncertainty of $1.3\times10^{-16}$ and optical frequency comparisons with clocks based on $^{171}$Yb$^+$ (E3) and $^{87}$Sr. With a fractional uncertainty of $4.4\times10^{-18}$, the former is - to our knowledge - the most accurate frequency ratio value reported to date. For the $^{115}$In$^+$/$^{87}$Sr ratio, we improve upon the best previous measurement by more than an order of magnitude. We also demonstrate operation with four $^{115}$In$^+$ clock ions, which reduces the instability to $9.2\times10^{-16}/\sqrt{\tau/1\;\mathrm{s}}$.

physics.atom-ph↗

arXiv2023

Bichromatic UV detection system for atomically-resolved imaging of ions

We present a compact and bichromatic imaging system, located outside of the vacuum chamber of a trapped ion apparatus, that collects the fluorescence of 230.6 nm and 369.5 nm photons simultaneously on a shared EMCCD camera. The system contains two lens doublets, consisting of a sphere and an asphere. It provides a numerical aperture of 0.45 and 0.40 at 230.6 nm and 369.5 nm, respectively, and enables spatially resolved state detection with a large field of view of 300 $μ$m for long $^{115}$In$^+$/$^{172}$Yb$^+$ Coulomb crystals. Instead of diffraction limited imaging for one wavelength, the focus in this system is on simultaneous single-ion resolved imaging of both species over a large field with special attention to the deep UV wavelength (230.6 nm) and the low scattering rate of In$^+$ ions. The introduced concept is applicable to other dual-species applications.

physics.atom-ph↗

arXiv2023

Sub-kelvin temperature management in ion traps for optical clocks

The uncertainty of the ac Stark shift due to thermal radiation represents a major contribution to the systematic uncertainty budget of state-of-the-art optical atomic clocks. In the case of optical clocks based on trapped ions, the thermal behavior of the rf-driven ion trap must be precisely known. This determination is even more difficult when scalable linear ion traps are used. Such traps enable a more advanced control of multiple ions and have become a platform for new applications in quantum metrology, simulation and computation. Nevertheless, their complex structure makes it more difficult to precisely determine its temperature in operation and thus the related systematic uncertainty. We present here scalable linear ion traps for optical clocks, which exhibit very low temperature rise under operation. We use a finite-element model refined with experimental measurements to determine the thermal distribution in the ion trap and the temperature at the position of the ions. The trap temperature is investigated at different rf-drive frequencies and amplitudes with an infrared camera and integrated temperature sensors. We show that for typical trapping parameters for $\mathrm{In}^{+}$, $\mathrm{Al}^{+}$, $\mathrm{Lu}^{+}$, $\mathrm{Ca}^{+}$, $\mathrm{Sr}^{+}$ or $\mathrm{Yb}^{+}$ ions, the temperature rise at the position of the ions resulting from rf heating of the trap stays below 700 mK and can be controlled with an uncertainty on the order of a few 100 mK maximum.

physics.atom-ph↗

arXiv2018

Controlling systematic frequency uncertainties at the $10^{-19}$ level in linear Coulomb crystals

Trapped ions are ideally suited for precision spectroscopy, as is evident from the remarkably low systematic uncertainties of single-ion clocks. The major weakness of these clocks is the long averaging time, necessitated by the low signal of a single atom. An increased number of ions can overcome this limitation and allow for the implementation of novel clock schemes. However, this presents the challenge to maintain the excellent control over systematic shifts of a single particle in spatially extended and strongly coupled many-body systems. We measure and deduce systematic frequency uncertainties related to spectroscopy with ion chains in a newly developed rf trap array designed for precision spectroscopy on simultaneously trapped ion ensembles. For the example of an In${}^+$ clock, sympathetically cooled with Yb${}^+$ ions, we show in our system that the expected systematic frequency uncertainties related to multi-ion operation can be below $1\times10^{-19}$. Our results pave the way to advanced spectroscopy schemes such as entangled clock spectroscopy and cascaded clock operation.

physics.atom-ph↗

arXiv2018

Probing Time Dilation in Coulomb Crystals in a high-precision Ion Trap

Trapped-ion optical clocks are capable of achieving systematic fractional frequency uncertainties of $10^{-18}$ and possibly below. However, the stability of current ion clocks is fundamentally limited by the weak signal of single-ion interrogation. We present an operational, scalable platform for extending clock spectroscopy to arrays of Coulomb crystals consisting of several tens of ions, while allowing systematic shifts as low as $10^{-19}$. Using a newly developed technique, we observe 3D excess micromotion amplitudes inside a Coulomb crystal with atomic spatial resolution and sub-nanometer amplitude uncertainties. We show that in ion Coulomb crystals of 400$μ$m and 2mm length, time dilation shifts of In${}^+$ ions due to micromotion can be close to $1\times10^{-19}$ and below $10^{-18}$, respectively. In previous ion traps, excess micromotion would have dominated the uncertainty budget for spectroscopy of even a few ions. By minimizing its contribution and providing a means to quantify it, this work opens up the path to precision spectroscopy in many-body ion systems, enabling entanglement-enhanced ion clocks and providing a well-controlled, strongly coupled quantum system.

physics.atom-ph↗