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K. Beeks

Publications and source records attributed to K. Beeks.

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Exploring $\alpha$- and $\beta$-decay-induced quenching of the $^{229}$Th nuclear-clock isomer in solid-state hosts

The radiative decay dynamics of an ensemble of $^{229\mathrm{m}}$Th nuclei embedded in CaF$_2$ and MgF$_2$ is investigated. The isomer is populated through $\beta$ decay of $^{229}$Ac following ion implantation, and its radiative decay is detected using vacuum-ultraviolet spectroscopy and measured as a function of time. This allows to identify and quantify the quenching of the radiative-decay signal induced by $\alpha$ or $\beta$ radiation. The quenching probability density is determined in different CaF$_2$ crystals and in a MgF$_2$ crystal, revealing differences up to two orders of magnitude between the investigated samples and a strong dependence on the host material and defect densities. The results support a microscopic mechanism mediated by charge carriers in which electronic excitations created by the decay radiation are captured near Th defects, thereby favoring non-radiative decay channels.

nucl-ex

A thorium-229 optical nuclear clock with feedback loop

The laser-accessible nuclear transition in the thorium-229 isotope has been identified as a promising candidate for the realization of an optical nuclear clock. Such a nuclear clock might rival or outperform current optical clocks based on electron-shell transitions in atoms or ions, is expected to be more robust against external perturbations, and provides enhanced sensitivity in clock-based tests of fundamental principles of physics. Here, we implement a thorium-229 nuclear clock by stabilizing a continuous-wave laser to the 148 nm nuclear transition with rapid feedback based on continuous absorption spectroscopy. The thorium-229 nuclei are embedded into a millimeter-sized, room temperature calcium fluoride crystal. A subharmonic of the 148 nm radiation is continuously compared to a Yb+ single-ion clock. The nuclear clock shows a simple shot-noise limited scaling of the fractional frequency instability of $3\cdot 10^{-12} \sqrt{\tau/\text{s}}$ where $\tau$ is the averaging time, approaching $10^{-15}$ instabilities over 1 day of continuous operation. Improvements of the instability by several orders of magnitude can be projected for future solid-state nuclear clocks. We use the nuclear clock to constrain models of ultralight dark matter by searching for periodic fluctuations and slow drifts in the nuclear transition energy, on time scales between 20 s and 1 day. Drawing benefit from the enhanced sensitivity of the thorium-229 transition, these constraints compete with the best atomic clocks concerning dark matter coupling to photons and go beyond previous measurements regarding coupling to the strong force and quarks.

physics.atom-ph

Continuous-wave laser absorption spectroscopy of the Thorium-229 nucleus

A low-energy nuclear transition in the isotope thorium-229 has been excited in thorium-doped crystals with laser light. This opens the perspective towards a highly stable and robust solid-state optical nuclear clock. The required laser radiation at 148 nm wavelength has so far been produced using pulsed laser systems where only a small fraction of the incident photons has been resonant with the narrow nuclear transition. Here we show that the nuclear resonance can be excited with a continuous-wave narrow-bandwidth laser source with a power of less than 1 nW, and that the resonance signal can be detected in absorption rather than in fluorescence. This eliminates the slow nuclear fluorescence decay from the detection process and offers a considerable advantage for clock operation through fast signal acquisition. The VUV laser source is based on three sequential frequency doublings, starting from a diode laser at 1187 nm that is well suited for linewidth narrowing and for frequency comparisons with optical atomic clocks. We use absorption spectroscopy for the quantitative characterization of two different Th-centers in calcium fluoride crystal and measure the isomeric shift between them. One of the centers shows a very small static electric crystal field gradient 0.1 V/$\r{A}^2$, to be compared to gradients in the range of 100 V/$\r{A}^2$ observed earlier. This indicates a center with high symmetry of the ions surrounding the Th nucleus, promising nuclear resonance lines that are nearly independent of the lattice spacing.

physics.atom-ph

Laser-Induced Quenching of the Th-229 Nuclear Clock Isomer in Calcium Fluoride

The 10-minute radiative lifetime of the first excited $^{229}$Th$^{4+}$ nuclear state in ionic crystals provides narrow spectroscopic linewidths, enabling the realization of a solid-state nuclear clock. Due to the 4+ noble gas configuration, electronic readout or state initialization schemes known from atomic clocks are inaccessible. This elongates the interrogation cycle, which will deteriorate the clock performance. To address this limitation we demonstrate laser-induced quenching (LIQ) as a method of depumping the $^{229}$Th isomer population in CaF$_2$. We provide experimental evidence for LIQ at different wavelengths (148 - 420 nm) and temperatures (100 - 350 K), achieving a threefold reduction in the isomer lifetime with 20 mW of laser power.

physics.atom-ph

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