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Fock matrix

 

Fock matrix

In the Hartree–Fock method of quantum mechanics, the Fock matrix is a matrix approximating the single-electron energy operator of a given quantum system in a given set of basis vectors.[1]

It is most often formed in computational chemistry when attempting to solve the Roothaan equations for an atomic or molecular system. The Fock matrix is actually an approximation to the true Hamiltonian operator of the quantum system. It includes the effects of electron-electron repulsion only in an average way. Importantly, because the Fock operator is a one-electron operator, it does not include the electron correlation energy.

The Fock matrix is defined by the Fock operator. For the restricted case which assumes closed-shell orbitals and single-determinantal wavefunctions, the Fock operator for the i-th electron is given by:[2]

\hat F(i) = \hat h(i)+\sum_{ j=1 }^{n/2}[2 \hat J_j(i)-\hat K_j(i)]

where:

\hat F(i) is the Fock operator for the i-th electron in the system,
{\hat h}(i) is the one-electron hamiltonian for the i-th electron,
n is the number of electrons and \frac{n}{2} is the number of occupied orbitals in the closed-shell system,
\hat J_j(i) is the Coulomb operator, defining the repulsive force between the j-th and i-th electrons in the system,
\hat K_j(i) is the exchange operator, defining the quantum effect produced by exchanging two electrons.

The Coulomb operator is multiplied by two since there are two electrons in each occupied orbital. The exchange operator is not multiplied by two since it has a non-zero result only for electrons which have the same spin as the i-th electron.

For systems with unpaired electrons there are many choices of Fock matrices.

See also

References

  1. ^ Callaway, J. (1974). Quantum Theory of the Solid State. New York: Academic Press.  
  2. ^ Levine, I.N. (1991) Quantum Chemistry (4th ed., Prentice-Hall), p.403


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