Quantum-State-Sensitive Detection of Alkali Dimers on Helium Nanodroplets by Laser-Induced Coulomb Explosion
arXiv:2111.12540 · doi:10.1103/PhysRevLett.128.093201
Abstract
Rubidium dimers residing on the surface of He nanodroplets are doubly ionized by an intense fs laser pulse leading to fragmentation into a pair of ions. We show that the kinetic energy of the fragment ions can be used to identify dimers formed in either the X ground state or in the lowest-lying triplet state, a . From the experiment, we estimate the abundance ratio of dimers in the a and X states as a function of the mean droplet size and find values between 4:1 and 5:1. Our technique applies generally to dimers and trimers of alkali atoms, here also demonstrated for , , and , and will enable fs time-resolved measurements of their rotational and vibrational dynamics, possibly with atomic structural resolution.
5 pages, 4 figures
References in corpus (5)
- Calculations of static dipole polarizabilities of alkali dimers. Prospects for alignment of ultracold molecules
- Photoionizaton of Pure and Doped Helium Nanodroplets
- Control and femtosecond time-resolved imaging of torsion in a chiral molecule
- Wave packet dynamics of potassium dimers attached to helium nanodroplets
- Desorption Dynamics of Rb_2 Molecules off the Surface of Helium Nanodroplets
Cited by in corpus (4)
- Laser-induced Coulomb Explosion Imaging of Alkali Dimers on Helium Nanodroplets
- Nonadiabatic Laser-Induced Alignment Dynamics of Molecules on a Surface
- Time-resolved Coulomb explosion imaging of vibrational wave packets in alkali dimers on helium nanodroplets
- Magnetic deflection of high-spin sodium dimers formed on helium nanodroplets