Effect of an applied magnetic field on 84Sr n1D2 ultralong-range Rydberg dimers

The data sets are tabulated and, within each file, columns are labelled to describe the corresponding physical variables (please see the manuscript for exact definitions of the variables.) Fig.3 : Molecular potential as a function interatomic distance R together with the wavefunctions of the selected vibrational states.

Fig.4 : (a) Photoassociation spectrum (b) expectation value of rotational quantum number and standard variation, (c-g) wavefunctions of selected molecular eigenstates (in the absence of magnetic field) Fig.5 : (a,b) Photoassociation spectra (c,d) expectation values of rotational quantum number and standard variations (in the limit of strong magnetic field, M=1,2) Fig.6 : Spherical harmonics for l=2 with variaous m Fig.7 : Wavefunctions of selected molecular eigenstates from Fig.5 Fig.8 : (a,b) Photoassociation spectra (c) expectation values of rotational quantum number and standard variations (in the limit of strong magnetic field, M=0) Fig.9 : Wavefunctions of selected molecular eigenstates from Fig.8 Fig.10 : Molecular eigenenergies as a function of magnetic field Fig.11 : Photoassociation spectra at B=0.2G Fig.12 : Photoassociation spectra at B=1G Fig.13 : Photoassociation spectra at B=2G Fig.14 : Photoassociation spectra at B=6G Fig.15 : Wavefunctions of selected molecular eigenstates from Fig.14