Hund's rules
In atomic physics and quantum chemistry, Hund's rules refers to a set of rules that German physicist Friedrich Hund formulated around 1925, which are used to determine the term symbol that corresponds to the ground state of a multi-electron atom.
It can be shown that for full orbitals and suborbitals both the residual electrostatic energy (repulsion between electrons) and the spin–orbit interaction can only shift all the energy levels together.
Thus when determining the ordering of energy levels in general only the outer valence electrons must be considered.
Due to the Pauli exclusion principle, two electrons cannot share the same set of quantum numbers within the same system; therefore, there is room for only two electrons in each spatial orbital.
Hund's first rule states that the lowest energy atomic state is the one that maximizes the total spin quantum number for the electrons in the open subshell.
The orbitals of the subshell are each occupied singly with electrons of parallel spin before double occupation occurs.
(This is occasionally called the "bus seat rule" since it is analogous to the behaviour of bus passengers who tend to occupy all double seats singly before double occupation occurs.)
Two different physical explanations have been given[5] for the increased stability of high multiplicity states.
In the early days of quantum mechanics, it was proposed that electrons in different orbitals are further apart, so that electron–electron repulsion energy is reduced.
However, accurate quantum-mechanical calculations (starting in the 1970s) have shown that the reason is that the electrons in singly occupied orbitals are less effectively screened or shielded from the nucleus, so that such orbitals contract and electron–nucleus attraction energy becomes greater in magnitude (or decreases algebraically).
The electron configuration of Si is 1s2 2s2 2p6 3s2 3p2 (see spectroscopic notation).
The diagram shows the state of this term with ML = 1 and MS = 1.
This rule deals with reducing the repulsion between electrons.
In the latter case the repulsive force increases, which separates electrons.
For silicon there is only one triplet term, so the second rule is not required.
The lightest atom that requires the second rule to determine the ground state term is titanium (Ti, Z = 22) with electron configuration 1s2 2s2 2p6 3s2 3p6 3d2 4s2.
In this case the open shell is 3d2 and the allowed terms include three singlets (1S, 1D, and 1G) and two triplets (3P and 3F).
(Here the symbols S, P, D, F, and G indicate that the total orbital angular momentum quantum number has values 0, 1, 2, 3 and 4, respectively, analogous to the nomenclature for naming atomic orbitals.)
are the components of the total orbital angular momentum L and total spin S along the z-axis chosen as the direction of an external magnetic field.)
This rule considers the energy shifts due to spin–orbit coupling.
In the case where the spin–orbit coupling is weak compared to the residual electrostatic interaction,
This term gives the dependence of the ground state energy on the magnitude of
lowest energy term of Si consists of three levels,
Hund's rules work best for the determination of the ground state of an atom or molecule.
They are also fairly reliable (with occasional failures) for the determination of the lowest state of a given excited electronic configuration.
Thus, in the helium atom, Hund's first rule correctly predicts that the 1s2s triplet state (3S) is lower than the 1s2s singlet (1S).
Similarly for organic molecules, the same rule predicts that the first triplet state (denoted by T1 in photochemistry) is lower than the first excited singlet state (S1), which is generally correct.
However Hund's rules should not be used to order states other than the lowest for a given configuration.
[5] For example, the titanium atom ground state configuration is ...3d2 for which a naïve application of Hund's rules would suggest the ordering 3F < 3P < 1G < 1D < 1S.
