Tim F. Wohlers-Reichel

We characterise an efficient optically-heated neutral atom source for ion trapping. We observe loading rates of up to $24(3)\,\mathrm{s}^{-1}$ with heating powers below $85\,\mathrm{mW}$, and demonstrate loading of a single ion in under $30\,\mathrm{s}$ with $41.4(4)\,\mathrm{mW}$ of optical power in a room-temperature ion trap system with an ionisation probability of $1.50(5)\times10^{-5}$. We calibrate a thermal model for the source's internal temperature by imaging the fluorescence of a collimated flux of neutral calcium that effuses from the oven at various optical heating powers. We show that the thermal performance of this oven is mainly limited by radiative losses. We explore the effect of second-stage photo-ionisation laser power on the loading rate, and identify a path beyond the loading rates reported in this study. We predict that this source is also well-suited to a wide range of metals used in ion-trapping.

Spectroscopy is one of the most accurate probes of the molecular world. However, predicting molecular spectra accurately is computationally difficult because of the presence of entanglement between electronic and nuclear degrees of freedom. Although quantum computers promise to reduce this computational cost, existing quantum approaches rely on combining signals from individual eigenstates, an approach that is difficult to scale because the number of eigenstates grows exponentially with molecule size. Here, we introduce a method for scalable analog quantum simulation of molecular spectroscopy, by performing simulations in the time domain. Our approach can treat more complicated molecular models than previous ones, requires fewer approximations, and can be extended to open quantum systems with minimal overhead. We present a direct mapping of the underlying problem of time-domain simulation of molecular spectra to the degrees of freedom and control fields available in a trapped-ion quantum simulator. We experimentally demonstrate our algorithm on a trapped-ion device, exploiting both intrinsic electronic and motional degrees of freedom, showing excellent quantitative agreement for a single-mode vibronic photoelectron spectrum of SO$_2$.