SearcharxivSearch

arXiv · 1404.6622

Tuning a magnetic Feshbach resonance with spatially modulated laser light

Abstract

We theoretically investigate the control of a magnetic Feshbach resonance using a bound-to-bound molecular transition driven by spatially modulated laser light. Due to the spatially periodic coupling between the ground and excited molecular states, there exists a band structure of bound states, which can uniquely be characterized by some extra bumps in radio-frequency spectroscopy. With the increasing of coupling strength, the series of bound states will cross zero energy and directly result in a number of scattering resonances, whose position and width can be conveniently tuned by the coupling strength of the laser light and the applied magnetic field (i.e., the detuning of the ground molecular state). In the presence of the modulated laser light, universal two-body bound states near zero-energy threshold still exist. However, compared with the case without modulation, the regime for such universal states is usually small. An unified formula which embodies the influence of the modulated coupling on the resonance width is given. The spatially modulated coupling also implies a local spatially varying interaction between atoms. Our work proposes a practical way of optically controlling interatomic interactions with high spatial resolution and negligible atomic loss.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Yi-Cai Zhang, Wu-Ming Liu, Hui Hu. 2014-11-21. Tuning a magnetic Feshbach resonance with spatially modulated laser light. https://doi.org/10.1103/physreva.90.052722

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