[Pw_forum] Why the energies are different when two molecules are calculated together and separate?
Nichols A. Romero
naromero at gmail.com
Wed Apr 12 20:06:57 CEST 2006
Xunlei,
I am not surprised that your two calculations:
E(CO2) and E(H) separate supercells
versus
E(CO2+H) same supercell
give different energies, even if they are well separated in a *huge* empty box.
My former adviser, Richard Martin, tells me this is *famous* DFT problem.
See,
C. Almbladh and U. von Barth, "Exact results for the charge and spin
densities, exchange-correlation potentials, and density-functional
eigenvalues," Phys. Rev. B 31:3231, 1985.
The *fundamental* problem is not with the basis set. "The general gist
is that the exact functional must be discontinuous at integer
occupations. This shows the problems with any functional that does
not have discontinuities - like LDA and GGA!", my former adviser. So,
I think if you have an asymptotically corrected functional, and I
don't know of any publicly available code that have this available,
you wouldn't have this problem.
I tried a similar test in SIESTA not too long ago. And even with an
LCAO basis set, you will see charge transfer in the combined systems
that is well separated in a *huge* empty box. It will be a *very*
small charge transfer but its there! Because of this small charge
transfer, there will be an energy difference between the two
calculations.
Bests,
On 4/12/06, Lucas Fernandez Seivane <quevedin at gmail.com> wrote:
> I believe that this is more or less the case that Prof. Marzari states
> as 1). It may due to an effect well known related to localized basis
> (LCAO, gaussians) which has to do with the number of wavefunctions in
> each one of your simulations: the Basis Set Superposition Error.
> Quoting from http://iqc.udg.es/~perico/bbopt.html:
> "The theoretical study of molecular interactions under the
> supermolecular approach with finite basis sets centered at the atomic
> positions originates the so-called Basis Set Superposition Error
> (BSSE) Within the LCAO-MO approach, each fragment can be expanded to
> some extent in the basis set of the partner. Thus, BSSE is the
> unphysical effect due to the improvement of the quantum mechanical
> description of the fragments within the supermolecule. It has been
> recognised for long time that this effect results in an increase of
> the interaction energy."
>
> Some ideas for dealing with it are seen for instance in
> http://arxiv.org/PS_cache/physics/pdf/9908/9908022.pdf or in
> http://dx.doi.org/10.1103/PhysRevB.72.075431
>
> On 4/12/06, Nicola Marzari <marzari at mit.edu> wrote:
> >
> >
> > My guess is that if you make your cell larger and larger the difference
> > will, very slowly, disappear.
> >
> > You have two sources of error
> >
> > 1) the "covalent" interaction between CO2 and H. You do not see this
> > in Gaussian because of the shortcomings of the basis set there -
> > there are no states able to represent the weak overlap of wavefunctions
> > midway between the molecule and the atom.
> >
> > 2) the dipole of the system, that interacts with itself periodically
> > repeated. See e.g. Makov Payne PRB 1995, or cond-mat/0602599 and Refs.
> > [14] in it.
> >
> > Let us know if 1) or 2) are to blame.
> >
> > nicola
> >
> >
> >
> > Xunlei Ding wrote:
> >
> > > Dear all,
> > > In a supercell (15A^3), I calculated the energies of one CO2 molecule,
> > > and a H atom, separately.
> > > I got the energies E(CO2) and E(H). Then I calculated the system
> > > contained both CO2 and H in the same supercell, and get the energy
> > > E(CO2+H).
> > > It is surprising to me that E(CO2+H) is lower than E(CO2)+E(H) by about
> > > more than 0.1eV.
> > > All calculations are used PBE functional and with Gamma point.
> > > I have put the H atom from CO2 at different places and the distances are
> > > tested for 6A and 9A. The cutoff are tested for 24Ry and 32Ry. The
> > > supercell are tested for 15A^3 and 20A^3. All these tests give the
> > > similar results and the energies differences are still more than 0.1eV.
> > >
> > > Then with Gaussian03, both with PBC (period boundary conditions) and
> > > without PBC (just free molecules), the results show that E(CO2+H) is
> > > very close to E(CO2)+E(H).
> > >
> > > It is found that the HOMO of H atom is also the HOMO of the system
> > > H+CO2, but in PWSCF results, HOMO of (H+CO2) is lower than that in H
> > > atom by ahout 0.1eV, while in Gaussian03 calculation, the HOMO is almost
> > > the same in H+CO2 and H . This is the reason why the total energy of
> > > H+CO2 is lower than E(H) + E(CO2).
> > >
> > > I want to know the reason for this energy difference.
> > >
> > > Thank you!
> > >
> > > Yours sincerely,
> > > Ding
> > >
> > >
> > >
> > > _______________________________________________
> > > Pw_forum mailing list
> > > Pw_forum at pwscf.org
> > > http://www.democritos.it/mailman/listinfo/pw_forum
> >
> > --
> > ---------------------------------------------------------------------
> > Prof Nicola Marzari Department of Materials Science and Engineering
> > 13-5066 MIT 77 Massachusetts Avenue Cambridge MA 02139-4307 USA
> > tel 617.4522758 fax 2586534 marzari at mit.edu http://quasiamore.mit.edu
> > _______________________________________________
> > Pw_forum mailing list
> > Pw_forum at pwscf.org
> > http://www.democritos.it/mailman/listinfo/pw_forum
> >
> _______________________________________________
> Pw_forum mailing list
> Pw_forum at pwscf.org
> http://www.democritos.it/mailman/listinfo/pw_forum
>
--
Nichols A. Romero, Ph.D.
1613 Denise Dr. Apt. D
Forest Hill, MD 21050
443-567-8328 (C)
410-306-0709 (O)
More information about the users
mailing list