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Compounds of polyatomic anions are investigated theoretically as hosts for thorium in nuclear clock devices. 

Laser cooling of large, complex molecules is a long-standing goal, instrumental for enabling new quantum technology and precision measurements. A primary consideration for the feasibility of laser cooling, which determines the efficiency and technical requirements of the process, is the number of excited-state decay pathways leading to vibrational excitations. Therefore, the assessment of the laser-cooling potential of a molecule begins with estimate of the vibrational branching ratios of the first few electronic excited states theoretically to find the optimum cooling scheme. Such calculations, typically done within the Born-Oppenheimer and harmonic approximations, have suggested that one leading candidate for large, polyatomic molecule laser cooling, alkaline earth phenoxides, can most efficiently be laser cooled via the third electronically excited ( $\tilde{C}$) state. Here, we report the first detailed spectroscopic characterization of the $\tilde{C}$state in CaOPh and SrOPh. We find that nonadiabatic couplings between the $\tilde{A}, \tilde{B}$, and $\tilde{C}$states lead to substantial mixing, giving rise to vibronic states that enable additional decay pathways. Based on the intensity ratio of these extra decay channels, we estimate a nonadiabatic coupling strength of $\sim 0.1{\mathrm{cm}}^{-1}$. While this coupling strength is small, the large density of vibrational states available at photonic energy scales in a polyatomic molecule leads to significant mixing. Only the lowest excited state $\tilde{A}$is exempt from this coupling because it is highly separated from the ground state. Thus, this result is expected to be general for large molecules and implies that only the lowest electronic excited state should be considered when judging the suitability of a molecule for laser cooling. 

The population dynamics of the ${}^{229}\mathrm{Th}$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 band gap opens an internal conversion decay channel, is presented and appears to reproduce the measured cross-section. By engineering defects into ${}^{229}\mathrm{Th}$-doped solid-state hosts, this previously unrecognized photoquenching process may be used to reduce the clock transition readout time and thereby increase the stability of the nuclear clock. Published by the American Physical Society2025