Why exchange-correlation effects reduces the energy?

In summary, the exchange-correlation effect in a two-electron system with same spins reduces the energy of the system by decreasing the Coulomb repulsion between the electrons. This effect is due to the antisymmetric nature of the wavefunction, which causes the average distance between same-spin electrons to be greater. In a N-electron system, the same effect can be seen by adding an "exchange-correlation hole + extra electron" to the system, which results in a greater interaction energy compared to the interaction energy of the electron with "N other electrons + one hole." This is because the hole has a positive charge, leading to extra attraction between the electrons.
  • #1
hokhani
483
8
Consider a two-electron system in which both of electrons have the same spins. They like to repel each other and so it seems that the energy of the system will increase compared with the situation in which two-electron system is composed of opposite spins that they can settle in the same place.
On the other hand we read that exchange-correlation effect is due to electrons with the same spins and reduce the energy of the system. I can't understand why this effect reduce the energy!
 
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  • #2
The splitting of energy into exchange and correlation is kind of artificial.
In Hartree theory the electronic wavefunction is represented as a simple product of molecular orbitals. Going to the single determinantal Hartree-Fock wavefunction yields the exchange correction. The difference between the true energy and the Hartree-Fock energy is the correlation energy.

In the sense of a variational approximation, the wavefunction becomes more and more complex when going from Hartree to Hartree-Fock to the true wavefunction. So the energy at least of the ground state can only get lower.

The Hartree ansatz violates the Pauli principle inasfar as atoms with the same spin can be at the same place. If the electrons were neutral this would not be a big problem and lead only to relatively small errors in the kinetic energy. However as electrons are charged, this also overestimates strongly the Coulombic repulsion between the electrons.
Going to Hartree-Fock thus reduces the Coulomb repulsion between electrons with parallel spins which comes out to large in the Hartee approximation.
 
  • #3
Thanks Mr/Mis DrDu, I got convinced. But for an electron in a N-electron system we regard this effect equivalent to adding "exchange-correlation hole + extra electron" to the system. Why for a N-electron system;
Interaction energy of an electron with N-1 other electrons > Interaction energy of that electron with "N other electrons+one hole"?
 
  • #4
Because a hole by definition has a positive charge and thus you get extra attraction?
 
  • #5
Well, if you don't believe it, calculate it yourself with the Heitler London wavefunctions!

This is done in Ashcroft + Mermin, if you want a reference.

The point is that the total many electron wavefunction must be antisymmetric with respect to interchange of the two electrons. If the two spins are the same, then the spatial part must carry the antisymmetry. This implies that two-electron wavefunction vanishes if we try to put the electrons close together. This has nothing to do with the interactions between the electrons - it's just the nature of the wavefunction. In the end, this implies the average distance between two electrons with the same spin is greater, so they feel less Coulomb repulsion. As far as I know, the kinetic energy of the singlet and triplet wavefunctions is actually the same in the Heitler London picture.
 

1. Why do we need to account for exchange-correlation effects in energy calculations?

Exchange-correlation effects refer to the interactions between electrons in a system, and they play a crucial role in determining the energy of a system. Ignoring these effects can lead to inaccurate results, as they can significantly contribute to the overall energy of a system.

2. How do exchange-correlation effects affect the energy of a system?

Exchange-correlation effects can both increase and decrease the energy of a system. They can increase the energy by causing repulsion between like-charged electrons, or decrease the energy by promoting bonding between electrons of opposite spin.

3. Can exchange-correlation effects be accurately calculated?

While there are various methods for approximating exchange-correlation effects, it is challenging to accurately calculate them due to their complex nature. Therefore, most calculations rely on approximations and empirical models.

4. How do exchange-correlation effects differ between different materials?

The strength and nature of exchange-correlation effects can vary greatly between different materials. This is due to differences in the electronic structure and bonding between atoms in different materials, which can affect the interactions between electrons.

5. Can exchange-correlation effects be neglected in certain systems?

In some cases, such as in simple systems with a small number of electrons, exchange-correlation effects may have a negligible impact on the overall energy. However, it is generally recommended to account for these effects in energy calculations to ensure accuracy.

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