Isolated-core excitations in strong electric fields. I. Theory
F. Robicheaux
Department of Physics, Auburn University, Auburn, Alabama 36849
Received 14 January 2000; published 17 August 2000
A basic theory is presented for the photoexcitation of a core state of a Rydberg atom in any type of static
field; in this situation, the core state is excited by the photon while the Rydberg electron is essentially a
spectator. This simple picture is made interesting through the interaction of the Rydberg electron with the core
which can cause a change in the Rydberg electron’s state and can cause the Rydberg electron to autoionize.
The method is computationally efficient and has been used for alkaline-earth atoms in a static electric field. An
approximation to the formalism is presented that illustrates a mechanism controlling the isolated core excita-
tion in a static electric field; this approximation may serve as a paradigm for extending the interpretation of
isolated core spectra to other types of fields.
PACS numbers: 32.60.+i, 32.80.Dz, 32.80.Rm
I. INTRODUCTION
There are many tools that have been used to probe corre-
lation in many electron atoms. The study of photoabsorption
spectra is especially useful since the high resolution of the
laser allows precise determination of the energies and widths
of the states while the strength of transitions contains infor-
mation about the composition of the state. Most photoab-
sorption studies use compact initial states which thus probe
final-state correlation as manifested near the nucleus. By
contrast, the technique known as isolated core excitation uti-
lizes a highly excited initial state 1–8. With this technique,
the atom is initially prepared such that one electron is excited
to a Rydberg state with the remaining electrons left in the
ground state of the positive ion. A second laser is then
scanned over optically allowed transitions of the positive ion.
A large ionization signal is observed at the frequencies of
optically allowed transitions in the core; ionization is also
observed at other frequencies because both the core and the
Rydberg electron can simultaneously make transitions due to
the electron-core interaction.
The isolated core excitation directly probes the interaction
of the Rydberg electron with the core electrons. In the exci-
tation process, the core changes character which thus
changes the potential for the Rydberg electron. The strength
of the excitation to the final state depends almost solely on
the projection of the initial Rydberg wave function onto the
final Rydberg wave function. If the potential for the Rydberg
electron is unchanged, then only one final state is excited. As
the change in the potential increases, then the character of
the final states change and increasingly many final states can
be excited. The electron-core interaction is also manifested
through the autoionization widths of the final states. Often,
the resonance widths can be measured quite simply using
isolated core excitations because there is very little direct
excitation to the open channels. Thus, there is little interfer-
ence between the direct ionization path and the indirect ion-
ization path through the resonance states; the photoabsorp-
tion cross section near a resonance is often a simple
Lorentzian.
In the past, most isolated core experiments and all isolated
core calculations were for atoms unperturbed by static fields.
Two previous studies presented experimental results for iso-
lated core excitations by a cw laser for Mg in a static electric
field 6 and by a pulsed laser for Mg in a static electric field
7. It is important to extend the study of isolated core exci-
tations to atoms in strong, static fields. Photoionization by
isolated core excitations is the time reverse of dielectronic
recombination DR. In DR, an electron scatters from an ion,
excites the ion so that it is captured into a doubly excited
resonance state, and is stabilized when the core electrons
emit a photon. It is known that static electric fields for ex-
ample, the microfields that exist in plasmas can affect the
recombination rate due to the l mixing of the autoionizing
Rydberg states 9,10. Early measurements 11 and calcula-
tions 12 showed the effect of electric fields on a Rydberg
series. However, it has not yet been possible to perform de-
tailed comparisons between experimental and calculated re-
combination cross sections for individual resonances in a
static electric field; this is because the resolution in electron
scattering experiments is not high enough to resolve the Ry-
dberg states that are most strongly affected. The isolated core
excitations can be studied with high resolution since the limi-
tation is from the resolution of a laser. Thus, detailed com-
parison can be performed at the individual resonance level.
Finally, it is also worth studying isolated core excitations
in static electric fields as an interesting example of channel
interactions and correlations between different degrees of
freedom. The Hamiltonian for the nonrelativistic treatment
of a hydrogen atom in a static electric field separates in para-
bolic coordinates. However, the Hamiltonian does not sepa-
rate for any other atom in a static electric field. For a Ryd-
berg state with an excited ion core, the electron-electron
interactions can cause the Rydberg electron to scatter be-
tween different channels in parabolic coordinates while
keeping its total energy fixed; also, this interaction can cause
an exchange of energy between the Rydberg electron and the
ion which may lead to the ejection of an electron from the
atom. The competition and interplay between these two types
of correlation can give interesting features in the spectra. In
the isolated core excitation, the initial state is already a Ry-
dberg state and can be chosen to be a state that is essentially
an uncoupled state in parabolic coordinates or a state that is
essentially an angular momentum eigenstate; this leads to a
PHYSICAL REVIEW A, VOLUME 62, 033406
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