arXiv subjects

R. Elwell

Publications and source records attributed to R. Elwell.

7 recordsLinked to original sources

arXiv2026

Colloquium: Nuclear clocks

The Th-229 nuclear isomeric state has the lowest energy of all known nuclear excited states, placing it within the reach of current table-top laser technology. This extraordinary property has made this nuclear isomer an attractive candidate for a nuclear optical clock of incredibly high precision and accuracy, both as isolated trapped Th-229 ions and embedded into solid-state platforms. Activity around Th-229 has surged in recent years, driven by breakthroughs in its direct laser excitation. The underlying nuclear physics that gives rise to this unique isomer will be elucidated, as well as the nearly half-century of efforts that led to its direct excitation. The design and systematics of a Th-229 nuclear clock will be discussed, both in ion traps and in the solid-state. These systematics, such as frequency shifts and quenching channels, can be leveraged both to probe the local chemical environment, and as a control knob during clock operation. Finally, the nuclear clock's high sensitivity to the variations of fundamental constants will be discussed.

physics.atom-ph↗

arXiv2024

Photo-Induced Quenching of the 229Th Isomer in a Solid-State Host

The population dynamics of the 229Th isomeric state is studied in a solid-state host under laser illumination. A photoquenching process is observed, where off-resonant vacuum-ultraviolet (VUV) radiation leads to relaxation of the isomeric state. The cross-section for this photoquenching process is measured and a model for the decay process, where photoexcitation of electronic states within the material bandgap opens an internal conversion decay channel, is presented and appears to reproduce the measured cross-section.

physics.atom-ph↗

arXiv2024

Theory of internal conversion of the thorium-229 nuclear isomer in solid-state hosts

Laser excitation of thorium-229 nuclei in doped wide bandgap crystals has been demonstrated recently, opening the possibility of developing ultrastable solid-state clocks and sensitive searches for new physics. We develop a quantitative theory of the internal conversion of isomeric thorium-229 in solid-state hosts. The internal conversion of the isomer proceeds by resonantly exciting a valence band electron to a defect state, accompanied by multi-phonon emission. We demonstrate that, if the process is energetically allowed, it generally quenches the isomer on timescales much faster than the isomer's radiative lifetime, despite thorium being in the +4 charge state in the valence band.

physics.atom-ph↗

arXiv2024

229Th-doped nonlinear optical crystals for compact solid-state clocks

The recent laser excitation of the 229Th isomeric transition in a solid-state host opens the door for a portable solid-state nuclear optical clock. However, at present the vacuum-ultraviolet laser systems required for clock operation are not conducive to a fieldable form factor. Here, we propose a possible solution to this problem by using 229Th-doped nonlinear optical crystals, which would allow clock operation without a vacuum-ultraviolet laser system and without the need of maintaining the crystal under vacuum.

physics.optics↗

arXiv2024

$^{229}\mathrm{ThF}_4$ thin films for solid-state nuclear clocks

After nearly fifty years of searching, the vacuum ultraviolet $^{229}$Th nuclear isomeric transition has recently been directly laser excited [1,2] and measured with high spectroscopic precision [3]. Nuclear clocks based on this transition are expected to be more robust [4,5] than and may outperform [6,7] current optical atomic clocks. They also promise sensitive tests for new physics beyond the standard model [5,8,9]. In light of these important advances and applications, a dramatic increase in the need for $^{229}$Th spectroscopy targets in a variety of platforms is anticipated. However, the growth and handling of high-concentration $^{229}$Th-doped crystals [5] used in previous measurements [1-3,10] are challenging due to the scarcity and radioactivity of the $^{229}$Th material. Here, we demonstrate a potentially scalable solution to these problems by demonstrating laser excitation of the nuclear transition in $^{229}$ThF$_4$ thin films grown with a physical vapor deposition process, consuming only micrograms of $^{229}$Th material. The $^{229}$ThF$_4$ thin films are intrinsically compatible with photonics platforms and nanofabrication tools for integration with laser sources and detectors, paving the way for an integrated and field-deployable solid-state nuclear clock with radioactivity up to three orders of magnitude smaller than typical \thor-doped crystals [1-3,10]. The high nuclear emitter density in $^{229}$ThF$_4$ also potentially enables quantum optics studies in a new regime. Finally, we describe the operation and present the estimation of the performance of a nuclear clock based on a defect-free ThF$_4$ crystal.

physics.atom-ph↗

arXiv2024

Radiative Decay of the $^{229m}$Th Nuclear Clock Isomer in Different Host Materials

A comparative vacuum ultraviolet spectroscopy study conducted at ISOLDE-CERN of the radiative decay of the $^{229m}$Th nuclear clock isomer embedded in different host materials is reported. The ratio of the number of radiative decay photons and the number of $^{229m}$Th embedded are determined for single crystalline CaF$_2$, MgF$_2$, LiSrAlF$_6$, AlN, and amorphous SiO$_2$. For the latter two materials, no radiative decay signal was observed and an upper limit of the ratio is reported. The radiative decay wavelength was determined in LiSrAlF$_6$ and CaF$_2$, reducing its uncertainty by a factor of 2.5 relative to our previous measurement. This value is in agreement with the recently reported improved values from laser excitation.

nucl-ex↗

arXiv2024

Laser excitation of the $^{229}$Th nuclear isomeric transition in a solid-state host

LiSrAlF$_6$ crystals doped with $^{229}$Th are used in a laser-based search for the nuclear isomeric transition. Two spectroscopic features near the nuclear transition energy are observed. The first is a broad excitation feature that produces red-shifted fluorescence that decays with a timescale of a few seconds. The second is a narrow, laser-linewidth-limited spectral feature at $148.38219(4)_{\textrm{stat}}(20)_{\textrm{sys}}$ nm ($2020407.3(5)_{\textrm{stat}}(30)_{\textrm{sys}}$ GHz) that decays with a lifetime of $568(13)_{\textrm{stat}}(20)_{\textrm{sys}}$ s. This feature is assigned to the excitation of the $^{229}$Th nuclear isomeric state, whose energy is found to be $8.355733(2)_{\textrm{stat}}(10)_{\textrm{sys}}$ eV in $^{229}$Th:\thor:LiSrAlF$_6$.

physics.atom-ph↗