A variational calculation is presented of energy levels for the nonrelativistic Hamiltonian of the metastable antiprotonic helium atom
p3,4He+. This calculation is based on a molecular expansion of the wave function. We estimate the precision of the results to be about ${10}^{\ensuremath{-}7}$ a.u.
A very accurate variational expansion is suggested for calculation of nonrelativistic energies of the metastable antiprotonic helium atoms
He+p. This expansion reflects the dual atomic-molecular nature of the system. Convergence of the results as a function of the increasing sets of basis functions shows an accuracy better than ${10}^{\ensuremath{-}10}\mathrm{a}.\mathrm{u}.,$ two orders of magnitude better than in our previous calculations.
Metastable states of antiprotonic helium
pHe+ whose energies lie in the range of the
2S and
2P excited states of He are discussed and their energies are calculated using the hyperspherical method within the "symmetric top" approximation. These states can be populated via collisions of antiprotons with excited He atoms. They represent another group of the potentially observable metastable states of
pHe+, which are characterized by the total angular momentum $L\ensuremath{\sim}70$, in contrast to the recently discovered metastable states having $L\ensuremath{\sim}35$.
The exotic helium atom, consisting of a helium nucleus
He2+, an electron ${\mathit{e}}^{\mathrm{\ensuremath{-}}}$, and a massive, negatively charged particle ${\mathit{X}}^{\mathrm{\ensuremath{-}}}$, such as an antiproton (p\ifmmode\bar\else\textasciimacron\fi{}) or a kaon (${\mathit{K}}^{\mathrm{\ensuremath{-}}}$), is studied theoretically. This exotic atom is more like a polar molecule with two nuclei
He2+ and ${\mathit{X}}^{\mathrm{\ensuremath{-}}}$, if ${\mathit{e}}^{\mathrm{\ensuremath{-}}}$ is in a low-lying orbital and ${\mathit{X}}^{\mathrm{\ensuremath{-}}}$ is in a highly excited orbital. Such states are generally formed in the capture of ${\mathit{X}}^{\mathrm{\ensuremath{-}}}$ by helium. The Born-Oppenheimer (BO) separation of the ${\mathit{e}}^{\mathrm{\ensuremath{-}}}$ motion and the
He2+-${\mathit{X}}^{\mathrm{\ensuremath{-}}}$ motion is a good approximation for these states, and affords a transparent, unified perspective of exotic helium with different ${\mathit{X}}^{\mathrm{\ensuremath{-}}}$ and different isotopes of
He2+. A propensity rule that favors small transition energies (except for the smallest one) is found for radiative emission by low vibrational and high rotational levels. This rule resembles the selection rule for infrared emission by the usual diatomic polar molecules, and contradicts the conventional expectation that radiative transitions in exotic atoms favor larger transition energies. The radiative lifetimes \ensuremath{\tau} of highly excited states formed immediately after the capture of ${\mathit{X}}^{\mathrm{\ensuremath{-}}}$ are of the order of \ensuremath{\mu}sec for
4He2+-p\ifmmode\bar\else\textasciimacron\fi{}-${\mathit{e}}^{\mathrm{\ensuremath{-}}}$ and
3He2+-p\ifmmode\bar\else\textasciimacron\fi{}-${\mathit{e}}^{\mathrm{\ensuremath{-}}}$, and those for
4He2+-${\mathit{K}}^{\mathrm{\ensuremath{-}}}$-${\mathit{e}}^{\mathrm{\ensuremath{-}}}$ are about half the values for the antiprotonic helium.The effect of the electronic charge polarization by ${\mathit{X}}^{\mathrm{\ensuremath{-}}}$ on \ensuremath{\tau} is explained quantitatively in a simple picture in terms of the molecular dipole moment. Low vibrational, high rotational states are described as circular or near-circular states in the atomic picture. They are stable against Auger decay, which the nonadiabatic perturbation on the BO states induces. An infinite series of bound \ensuremath{\Sigma} electronic states of exotic helium negative ions (
He2+-${\mathit{X}}^{\mathrm{\ensuremath{-}}}$-${\mathit{e}}^{\mathrm{\ensuremath{-}}}$)-${\mathit{e}}^{\mathrm{\ensuremath{-}}}$ exists for any
He2+-${\mathit{X}}^{\mathrm{\ensuremath{-}}}$ distances R beyond 0.819 a.u. in the BO approximation. An infinite \ensuremath{\Pi} series exists for R>3.811 a.u., and an infinite \ensuremath{\Delta} series for R>9.532 a.u.
The cross sections and rates for quenching of thermalized antiprotonic helium atoms in binary collisions with ordinary helium atoms are calculated in perturbation theory and in the coupled-channel formalism at the temperature and the number density of the helium gas,
T=6K and $N={10}^{21}\phantom{\rule{0.3em}{0ex}}{\text{cm}}^{\ensuremath{-}3}$, respectively. It is shown that quenching is unlikely to be relevant for the metastable states of the antiprotonic helium atom with $32\ensuremath{\leqslant}n\ensuremath{\leqslant}40$. Comparison with experiment shows a good quantitative agreement for the
(n,l)=(39,35) state of antiprotonic helium and a large disagreement for the
(37,34) state. As a byproduct of this work, the existence of a series of bound states of the
He−−p4He+ dimer is demonstrated numerically for $n\ensuremath{\geqslant}38$.