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Helium and Other Two Electron Systems

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Atoms, Molecules and Optical Physics 1

Part of the book series: Graduate Texts in Physics ((GTP))

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Abstract

After a general introduction and a survey of the experimental observations (Sect. 7.1) the quantum mechanical basis for treating multi-electron systems is reviewed in Sect. 7.2. The reader should know about these tools or get used to them by reading this section. Section 7.3 expands this theme by introducing electron exchange and the characteristic excited state configurations. Fine structure interaction in He and He like ions are addressed in Sect. 7.4 – a consolidation of our knowledge acquired in Chap. 6 which will turn out to be essential also for later chapters. In Sect. 7.5 the most important selection rules for E1 transitions in multi-electron system are treated. This directly leads to “double excitation” in Sect. 7.6. It is of importance far beyond atomic physics: resonances of states imbedded into a continuum are found in all fields of physics. The ensuing interference structures, known as Fano resonances and their origin are described in a practical, easy to access approach. Finally, in Sect. 7.7 the alkaline earth atoms and the Hg atom are treated: they are related to He in an analogous manner as alkali atoms are related to the H atom.

So far our discussions were restricted to atomic systems with effectively one active electron in an attractive Coulomb or screened Coulomb field. For the majority of atoms this simple model cannot be maintained, since the electrons repel each other pairwise and have to obey the Pauli principle. The helium atom (He) is the simplest and purest example for introducing the key problems which one encounters in true multi-electron systems, as well as the methods for describing and understanding them.

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Notes

  1. 1.

    The difference is due to the necessary kinematic corrections with \(\bar{m}_{\mathrm{e}}/m_{\mathrm{e}}\) for finite mass and further corrections such as the Lamb shift.

  2. 2.

    If no ambiguities can arise, we abbreviate here and in the following r j and s j as well as q j by j.

  3. 3.

    We mention, however, a very remarkable property of this description of singlet states: the wave function (state) is not separable, i.e. we cannot write it as a simple direct product of states from the two separated electrons. One calls such states “entangled”, see also Appendix E.3.

  4. 4.

    Note that the signals shown are not generated by differentiation as often done in spectroscopy for better assignment of line centres – the genuine line shapes are shown here.

  5. 5.

    Two asterisks, short for double excitation.

  6. 6.

    For fitting a measured signal the original formula has to be slightly generalized, e.g. to

    $$ S(\epsilon)=\dfrac{C}{q^{2}+1}\dfrac{ ( q+\epsilon) ^{2}}{1+\epsilon^{2}}+ \biggl( A^{2}- \dfrac{C}{q^{2}+1} \biggr) , $$
    (7.69)

    accounting for the background signal A 2 and the strength C of the resonance.

  7. 7.

    One may derive from (7.74) with some algebra the modified Fano formula (7.69) with

    $$ C=AB\sqrt{4+\dfrac{4B}{A}\sin\delta+ \biggl( \dfrac{B}{A} \biggr) ^{2}}\quad\mbox{and}\quad q=-\dfrac{C/(AB)+B/A+2\sin\delta}{2\cos\delta}\quad\mbox{for }\cos\delta\neq0 $$

    q=0 for δ=π/2 and q→∞ for δ=−π/2; C and thus q are in principle double valued.

References

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Authors and Affiliations

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Acronyms and Terminology

a.u.:

‘atomic units’, see Sect. 2.6.2.

CI:

‘Configuration interaction’, mixing of states with different electronic configurations in atomic and molecular structure calculations, using linear superpositon of Slater determinants (see Sect. 10.2.3).

E1:

‘Electric dipole’, transitions induced by the interaction of an electric dipole with the electric field component of electromagnetic radiation.

FS:

‘Fine structure’, splitting of atomic and molecular energy levels due to spin orbit interaction and other relativistic effects (Chap. 6).

IR:

‘Infrared’, spectral range of electromagnetic radiation. Wavelengths between \(760\operatorname{nm}\) and \(1\operatorname{mm}\) according to ISO 21348 (2007).

NIST:

‘National institute of standards and technology’, located at Gaithersburg (MD) and Boulder (CO), USA. http://www.nist.gov/index.html.

SI:

‘Système international d’unités’, international system of units (m, kg, s, A, K, mol, cd), for details see the website of the Bureau International des Poids et Mésure http://www.bipm.org/en/si/ or NIST http://physics.nist.gov/cuu/Units/index.html.

UV:

‘Ultraviolet’, spectral range of electromagnetic radiation. Wavelengths between \(100\operatorname{nm}\) and \(400\operatorname{nm}\) according to ISO 21348 (2007).

VIS:

‘Visible’, spectral range of electromagnetic radiation. Wavelengths between \(380\operatorname{nm}\) and \(760\operatorname{nm}\) according to ISO 21348 (2007).

VUV:

‘Vacuum ultraviolet’, spectral range of electromagnetic radiation. Part of the UV spectral range. Wavelengths between \(10\operatorname{nm}\) and \(200\operatorname{nm}\) according to ISO 21348 (2007).

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Hertel, I.V., Schulz, CP. (2015). Helium and Other Two Electron Systems. In: Atoms, Molecules and Optical Physics 1. Graduate Texts in Physics. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-54322-7_7

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