The efficient production of very-high-
n, $n\ensuremath{\sim}300$, quasi-one-dimensional (quasi-1D) strontium Rydberg atoms through three-photon excitation of extreme Stark states in the presence of a weak dc field is demonstrated using a crossed laser-atom beam geometry. Strongly polarized quasi-1D states with large permanent dipole moments $\ensuremath{\sim}1.2{n}^{2}$ a.u. can be created in the beam at densities ($\ensuremath{\sim}{10}^{6}$ cm${}^{\ensuremath{-}3}$) where dipole blockade effects should become important. A further advantage of three-photon excitation is that the product
F states are sensitive to the presence of external fields, allowing stray fields to be reduced to very small values. The experimental data are analyzed using quantum calculations based on a two-active-electron model together with classical trajectory Monte Carlo simulations. These allow determination of the atomic dipole moments and confirm that stray fields can be reduced to $\ensuremath{\le}25\phantom{\rule{4pt}{0ex}}\ensuremath{\mu}$V cm${}^{\ensuremath{-}1}$.
The production of very-high-
n ($n\ensuremath{\sim}300$--500) strontium Rydberg atoms is explored using a crossed-laser-atom-beam geometry.
n1S0 and
n1D2 states are created by two-photon excitation via the
5s5p 1P1 intermediate state using radiation with wavelengths of $\ensuremath{\sim}$461 and $\ensuremath{\sim}$413 nm. Rydberg atom densities as high as $\ensuremath{\sim}3\ifmmode\times\else\texttimes\fi{}{10}^{5}$ cm${}^{\ensuremath{-}3}$ have been achieved, sufficient that Rydberg-Rydberg interactions can become important. The isotope shifts in the Rydberg series limits are determined by tuning the 461-nm light to preferentially excite the different strontium isotopes. Photoexcitation in the presence of an applied electric field is examined. The initially quadratic Stark shift of the
n1P1 and
n1D2 states becomes near-linear at higher fields and the possible use of
n1D2 states to create strongly polarized, quasi-one-dimensional electronic states in strontium is discussed. The data are analyzed with the aid of a two-active-electron (TAE) approximation. The two-electron Hamiltonian, within which the Sr
2+ core is represented by a semi-empirical potential, is numerically diagonalized allowing the calculation of the energies of high-
n Rydberg states and their photoexcitation probabilities.