A numerical method is presented to treat atoms in strong time-dependent electric fields. The method is applied to calculate ionization probabilities of H Rydberg atoms in strong monochromatic and bichromatic microwave fields. Recent experimental data on the microwave ionization of H Rydberg atoms are well reproduced. Ionization probabilities for microwave field parameters not yet covered experimentally are predicted. We propose to use the setup of existing two-frequency waveguide experiments to reveal the structure of the quasi-energy spectrum of microwave-driven Rydberg atoms. In analogy to dressed-state spectroscopy of atoms in strong laser fields, the quasi-energies of a periodically driven quantum system are mapped out by sweeping the frequency of a second (weak) additional rf probe field.
Excitation/ionization probabilities have been measured as a function of microwave electric amplitude F at three different microwave frequencies {omega}/2{pi} = 26.43, 30.36, 36.02 GHz for a wide range of initial no states of hydrogen Rydberg atoms. Using classically scaled variables n{sub 0}{sup 3}{omega}, n{sub 0}{sup 4}F, we discuss the scaling properties of these data. In particular, we note the scaling properties of nonclassical stability observed near n{sub 0}{sup 3}{omega} = 1.3. Our data support the assertion that this stability is due to the presence of a {open_quote}scarred{close_quote} wavefunction.
We have studied the ionization of Na ns and nd Rydberg atoms by \ensuremath{\sim}1-\ensuremath{\mu}s pulses of 10-MHz, 670-MHz, 2-GHz, and 4-GHz fields, bridging the gap between the previous measurements of ionization by \ensuremath{\sim}1-\ensuremath{\mu}s rise-time pulses and 8- and 15-GHz microwave fields. We have also studied the ionization of Li ns and nd Rydberg atoms by 4-, 8-, and 15-GHz fields, which, due to the smaller Li quantum defects, represents the high-frequency limit of nonhydrogenic microwave ionization. The Na measurements show that ionization at 10 MHz occurs without change in n at fields of 1/16
n4 and 1/9
n4. At 670 MHz \ensuremath{\Vert}m\ensuremath{\Vert}=0, 1, and 2 states are all ionized at fields between 1/3
n5 and 1/9
n4, indicating that transitions to higher-n states are occurring. As the frequency is raised further, to 2 and 4 GHz, the \ensuremath{\Vert}m\ensuremath{\Vert}=0 and 1 states exhibit an increasingly sharp threshold for ionization at E=1/3
n5, but the \ensuremath{\Vert}m\ensuremath{\Vert}=2 states are unlikely to ionize at this field, with ionization occurring mostly at higher fields, 1/3
n5E1/9
n4, approaching the 15-GHz behavior of ionization at E=1/9
n4. At 4 GHz, Li n=20 \ensuremath{\Vert}m\ensuremath{\Vert}=0 and 1 states ionize at E=1/3
n5, but at n\ensuremath{\simeq}45, \ensuremath{\Vert}m\ensuremath{\Vert}=1 states ionize at E=1/9
n4, and the \ensuremath{\Vert}m\ensuremath{\Vert}=0 states ionize at E>1/3
n5. The \ensuremath{\Vert}m\ensuremath{\Vert}=2 states appear to ionize at E=1/9
n4. As the frequency is raised to 8 and then to 15 GHz, the transition of \ensuremath{\Vert}m\ensuremath{\Vert}=0 and 1 states to ionization at E=1/9
n4 occurs at lower n. When a small static field is applied, the Li ionization threshold fields drop from 1/9
n4 to fields somewhat above 1/3
n5. Together the Na and Li measurements show that microwave ionization depends on a rate-limiting step, which is a resonant multiphoton transition.
We study experimentally and theoretically the detailed field-amplitude dependence of the multiphoton ionization and excitation probability of highly excited
n0 3S helium atoms in a 9.924-GHz linearly polarized microwave electric field. For ionization, with principal quantum numbers in the range
n0=25--32, we use a quasistatic analysis that employs integration of the time-dependent Schr\"odinger equation using basis states of the static field Hamiltonian. The calculated results are used to interpret the observed ionization threshold structure. For excitation, the results of
n0 3S\ensuremath{\rightarrow}
n0 3L, L>2 excitation experiments are explained quantitatively and precisely using a theory of multiphoton resonances. We present maps of quasienergy levels that allow the study of the dynamics of the field-switching transients. These transient effects are analyzed along the lines of standard atomic collision theory and are shown to determine the shape of the observed resonances.
The coherent interaction between ensembles of helium Rydberg atoms and microwave fields in the vicinity of a solid-state coplanar waveguide is reported. Rydberg-Rydberg transitions, at frequencies between 25 and 38 GHz, have been studied for states with principal quantum numbers in the range 30-35 by selective electric-field ionization. An experimental apparatus cooled to 100 K was used to reduce effects of blackbody radiation. Inhomogeneous, stray electric fields emanating from the surface of the waveguide have been characterized in frequency- and time-resolved measurements and coherence times of the Rydberg atoms on the order of 250 ns have been determined. These results represent a key element in the development of an experimental architecture to interface Rydberg atoms with solid-state devices.
Ionization of Rydberg atoms by short, half-cycle electrical pulses is investigated experimentally in the intermediate-pulse duration regime where the ionization threshold fields are determined both by the slew rate of the ionizing pulse and its duration. Electrical pulses with durations ranging from 140 ps to 9 ns and amplitudes up to are applied to rubidium and lithium atoms prepared in high Rydberg states by laser excitation (n ranges from 42 to 82). The amplitude of the 140 ps pulse required for ionization of the Rb and Li Rydberg population is found to be a factor of two higher than the expected amplitude based on diabatic field ionization and recent theoretical calculations by Reinhold et al (1993 26 L659). Using the longer pulses we studied the transition from the diabatic/adabatic ionization towards ionization in the impulse-kick regime.