pyscfad.dft.rks.RKS.get_veff

RKS.get_veff(mol=None, dm=None, dm_last=0, vhf_last=0, hermi=1)

Hartree-Fock potential matrix for the given density matrix

Args:

mol : an instance of Mole

dmndarray or list of ndarrays

A density matrix or a list of density matrices

Kwargs:

dm_lastndarray or a list of ndarrays or 0

The density matrix baseline. If not 0, this function computes the increment of HF potential w.r.t. the reference HF potential matrix.

vhf_lastndarray or a list of ndarrays or 0

The reference HF potential matrix.

hermiint

Whether J, K matrix is hermitian

0 : no hermitian or symmetric

1 : hermitian

2 : anti-hermitian

vhfopt :

A class which holds precomputed quantities to optimize the computation of J, K matrices

Returns:

matrix Vhf = 2*J - K. Vhf can be a list matrices, corresponding to the input density matrices.

Examples:

>>> import numpy
>>> from pyscf import gto, scf
>>> from pyscf.scf import _vhf
>>> mol = gto.M(atom='H 0 0 0; H 0 0 1.1')
>>> dm0 = numpy.random.random((mol.nao_nr(),mol.nao_nr()))
>>> vhf0 = scf.hf.get_veff(mol, dm0, hermi=0)
>>> dm1 = numpy.random.random((mol.nao_nr(),mol.nao_nr()))
>>> vhf1 = scf.hf.get_veff(mol, dm1, hermi=0)
>>> vhf2 = scf.hf.get_veff(mol, dm1, dm_last=dm0, vhf_last=vhf0, hermi=0)
>>> numpy.allclose(vhf1, vhf2)
True