Controlling $^{229}$Th isomeric state population in a VUV transparent crystal

TL;DR

This study demonstrates controlled population and depopulation of the $^{229}$Th isomeric state in a VUV transparent crystal, paving the way for solid-state nuclear clocks with potential applications in fundamental physics and precision timekeeping.

Contribution

The paper introduces a method for resonant X-ray pumping and controlled quenching of the $^{229}$Th isomer in a crystal, enabling on-demand population control crucial for nuclear clock development.

Findings

Measured isomer decay half-life of 447 ± 25 seconds.

Demonstrated a new X-ray quenching effect reducing half-life by at least a factor of 50.

Showed negligible non-radiative decay processes, supporting narrow linewidths for the transition.

Abstract

The radioisotope Th-229 is renowned for its extraordinarily low-energy, long-lived nuclear first-excited state. This isomeric state can be excited by VUV lasers and the transition from the ground state has been proposed as a reference transition for ultra-precise nuclear clocks. Such nuclear clocks will find multiple applications, ranging from fundamental physics studies to practical implementations. Recent investigations extracted valuable constraints on the nuclear transition energy and lifetime, populating the isomer in stochastic nuclear decay of U-233 or Ac-229. However, to assess the feasibility and performance of the (solid-state) nuclear clock concept, time-controlled excitation and depopulation of the $^{229}$Th isomer together with time-resolved monitoring of the radiative decay are imperative. Here we report the population of the $^{229}$Th isomeric state through resonant X-ray pumping and detection of the radiative decay in a VUV transparent $^{229}$Th-doped CaF$_2$ crystal. The decay half-life is measured to $447\pm 25$ s, with a transition wavelength of $148.18 \pm 0.42$ nm and a radiative decay fraction consistent with unity. Furthermore, we report a new ``X-ray quenching'' effect which allows to de-populate the isomer on demand and effectively reduce the half-life by at least a factor 50. Such controlled quenching can be used to significantly speed up the interrogation cycle in future nuclear clock schemes. Our results show that full control over the $^{229}$Th nuclear isomer population can be achieved in a crystal environment. In particular, non-radiative decay processes that might lead to a broadening of the isomer transition linewidth are negligible, paving the way for the development of a compact and robust solid-state nuclear clock. Further studies are needed to reveal the underlying physical mechanism of the X-ray quenching effect.