RESUMEN
The (229)thorium isotope presents an extremely low-energy isomer state of the nucleus which is expected around 7.8 eV, in the vacuum ultraviolet (VUV) regime. This unique system may bridge between atomic and nuclear physics, enabling coherent manipulation and precision spectroscopy of nuclear quantum states using laser light. It has been proposed to implant (229)thorium into VUV transparent crystal matrices to facilitate laser spectroscopy and possibly realize a solid-state nuclear clock. In this work, we validate the feasibility of this approach by computer modelling of thorium doping into calcium fluoride single crystals. Using atomistic modelling and full electronic structure calculations, we find a persistent large band gap and no additional electronic levels emerging in the middle of the gap due to the presence of the dopant, which should allow direct optical interrogation of the nuclear transition.Based on the electronic structure, we estimate the thorium nuclear quantum levels within the solid-state environment. Precision laser spectroscopy of these levels will allow the study of a broad range of crystal field effects, transferring Mössbauer spectroscopy into the optical regime.
Asunto(s)
Fluoruro de Calcio/análisis , Fluoruro de Calcio/química , Rayos Láser , Modelos Químicos , Física Nuclear/instrumentación , Análisis Espectral/instrumentación , Torio/análisis , Torio/química , Simulación por ComputadorRESUMEN
Understanding relaxation processes is an important unsolved problem in many areas of physics. A key challenge is the scarcity of experimental tools for the characterization of complex transient states. We used measurements of full quantum mechanical probability distributions of matter-wave interference to study the relaxation dynamics of a coherently split one-dimensional Bose gas and obtained comprehensive information about the dynamical states of the system. After an initial rapid evolution, the full distributions reveal the approach toward a thermal-like steady state characterized by an effective temperature that is independent from the initial equilibrium temperature of the system before the splitting process. We conjecture that this state can be described through a generalized Gibbs ensemble and associate it with prethermalization.