Physics:Hole formalism

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Hole formalism in quantum chemistry states that for many electronic properties, one may consider systems with e or (n-e), the number of unoccupied sites or "holes", to be equivalent.[1] The number of microstates (N) of a system corresponds to the total number of distinct arrangements for a number e of electrons to be placed in a number n of possible orbital positions: [math]\displaystyle{ N = \binom{n}{e} = \frac{n!}{e!(n-e)!} }[/math]

In hole formalism, the commutative property of multiplication applies, meaning that in the above equation, [math]\displaystyle{ e! \times (n-e)! = (n-e)! \times e! }[/math]

Example

For a set of p orbitals, n = 6 since there are two vacant positions in each of the three orbitals (px, py, pz). Therefore, for P2 (e = 2 and n = 6): [math]\displaystyle{ N = \binom{6}{2} = \frac{6!}{2!(6-2)!} = \frac{6 \times 5 \times 4 \times 3 \times 2 \times 1}{(2 \times 1) \times (4 \times 3 \times 2 \times 1)} = 15 }[/math]

Based on the hole formalism, microstates of P4 (e = 4 and n = 6) are: [math]\displaystyle{ N = \binom{6}{4} = \frac{6!}{4!(6-4)!} = 15 }[/math]

Here it is seen that P4 (2 holes) and P2 (4 holes) give equivalent values of N. The same is true for all p, d, f, ... systems such as d1/d9 or f2/f12.

This is characterised by the symmetry of k-combinations in general, that is: [math]\displaystyle{ \binom{n}{e} = \binom{n}{n - e} }[/math] For all positive integers n, e where ne.

See also

References

  1. K Veera Reddy (1998). Symmetry And Spectroscopy Of Molecules. New Age International. ISBN 8122411428.