SearcharxivSearch

arXiv · 2009.05211

Measuring the hyperfine splittings and deriving the hyperfine-interaction constants of Cesium 7D 5/2 excited state

Abstract

The measurement of Cesium (Cs) 7D5/2 excited state's hyperfine splitting intervals and hyperfine-interaction constants has been experimentally investigated based on ladder-type (852 nm + 698 nm) three-level Cs system (6S1/2 - 6P3/2 - 7D5/2) with room-temperature Cs atomic vapor cell. By scanning the 698-nm coupling laser's frequency, the Doppler-free high-resolution electromagnetically-induced transparency (EIT) assisted double-resonance optical pumping (DROP) spectra have been demonstrated via transmission enhancement of the locked 852-nm probe laser. The EIT-assisted DROP spectra are employed to study the hyperfine splitting intervals for the Cs 7D5/2 excited state with a room-temperature cesium atomic vapor cell, and the radio-frequency modulation sideband of a waveguide-type electro-optic phase modulator(EOPM) is introduced for frequency calibration to improve the accuracy of frequency interval measurement. The existence of EIT makes the DROP spectral linewidth much narrower, and it is very helpful to improve the spectroscopic resolution significantly. Benefiting from the higher signal-to-noise ratio (SNR) and much better resolution of the EIT-assisted DROP spectra, the hyperfine splitting intervals between the hyperfine folds of (F" = 6), (F" = 5), and (F" = 4) of cesium 7D5/2 state (HFS6"-5" = -10.60(0.17) MHz and HFS5"-4" = -8.54(0.15) MHz) have been measured, and therefore the magnetic-dipole hyperfine-interaction constant (A = -1.70(0.03) MHz) and the electric-quadrupole hyperfine-interaction constant (B = -0.77(0.58) MHz) have been derived for the Cs 7D5/2 state. These constants have important reference value for the improvement of precise measurement and determination of basic physical constants.

Explore related subjects

Keep this discovery

BibTeXRIS

Zerong Wang, Xiaokai Hou, Jiandong Bai, Junmin Wang. 2020-09-11. Measuring the hyperfine splittings and deriving the hyperfine-interaction constants of Cesium 7D 5/2 excited state. https://arxiv.org/abs/2009.05211

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Delay-engineered dynamical phases in a programmable non-Markovian spin oscillator

Non-Markovian dynamics offer a new route towards engineering non-equilibrium matter, where memory and feedback act as programmable resources for controlling order in time. Here we report the realization of a non-Markovian spin oscillator in a hot vapour $^{129}$Xe-Cs co-magnetometer with programmable feedback delay and gain. By tuning these parameters, we observe a hierarchy of dynamical phases, including time-crystalline response, nonlinear bifurcations, and frequency-comb formation. The measured spectra and phase boundaries are captured by linear stability analysis of delayed Bloch equations, revealing these phenomena as different manifestations of the same memory-induced instability structure. These results establish time-delayed feedback as a powerful strategy for controlling non-equilibrium phases, enabling quantum sensing, frequency referencing, and synchronization within a single spin-based platform.

physics.atom-ph

Non-stick vacuum wall collisions with a laser-coolable molecule

Molecular species that are suitable for direct laser cooling are typically considered lost or destroyed if they collide with an ambient temperature vacuum wall. Here, we study surface collisions with aluminum monofluoride (AlF), a laser-coolable molecule that survives this process with unusually high probability. We detect the outgoing AlF molecules from a single wall collision via Doppler-sensitive laser-induced fluorescence spectroscopy, using incoming supersonic (pulsed) and thermochemical (continuous) molecular beams. The angular, velocity and rovibrational level distributions of the outgoing molecules show near-complete thermalisation to the wall in a single collision event. We determine an upper limit to the surface residence time of about 5$~\mu$s, and by monitoring the decay in density of pulses of molecules loaded into a small storage volume, we deduce the surface sticking probability for different materials. For a siloxane-coated metallic surface, the sticking probability of AlF is about 0.015, allowing us to accumulate molecules from the thermochemical source into an ambient temperature storage vessel at densities near $10^{8}~$cm$^{-3}$. This provides a route to compact, portable traps for neutral molecules.

physics.atom-ph

Kinetic modeling of molecular beam formation in a cryogenic buffer-gas cell

Cryogenic buffer-gas cells are widely used to produce cold molecular beams, but the microscopic dynamics governing beam formation remain challenging to model. Here we present fully kinetic simulations of a cryogenic buffer-gas cell using the Direct Simulation Monte Carlo method implemented in the PICLas framework, treating the buffer gas and ablated molecules within a single unified model. We capture characteristic features of cryogenic buffer-gas sources, including plume cooling, directed transport toward the aperture, and the formation of a slow molecular beam, while also resolving energy transfer from the hot ablation plume to the helium buffer gas that is inaccessible to existing approaches relying on the background-gas approximation. Our results demonstrate that fully kinetic simulations can provide detailed insights into buffer-gas cell dynamics and open a route toward a systematic optimization of such sources.

physics.atom-ph