def lanczos_minmax(F,S=None,**kwargs):
"Estimate the min/max evals of F using a few iters of Lanczos"
doS = S is not None
niter = kwargs.get('niter',8)
N = F.shape[0]
niter = min(N,niter)
x = zeros(N,'d')
x[0] = 1
q = x
avals = []
bvals = []
if doS:
r = matrixmultiply(S,q)
else:
r = q
beta = sqrt(matrixmultiply(q,r))
wold = zeros(N,'d')
for i in xrange(niter):
w = r/beta
v = q/beta
r = matrixmultiply(F,v)
r = r - wold*beta
alpha = matrixmultiply(v,r)
avals.append(alpha)
r = r-w*alpha
if doS:
q = solve(S,r)
else:
q = r
beta = sqrt(matrixmultiply(q,r))
bvals.append(beta)
wold = w
E,V = eigh(tridiagmat(avals,bvals))
return min(E),max(E)
def lanczos_minmax(F, S=None, **kwargs):
"Estimate the min/max evals of F using a few iters of Lanczos"
doS = S is not None
niter = kwargs.get('niter', settings.DMPLanczosMinmaxIters)
N = F.shape[0]
niter = min(N, niter)
x = zeros(N, 'd')
x[0] = 1
q = x
avals = []
bvals = []
if doS:
r = matrixmultiply(S, q)
else:
r = q
beta = sqrt(matrixmultiply(q, r))
wold = zeros(N, 'd')
for i in xrange(niter):
w = r / beta
v = q / beta
r = matrixmultiply(F, v)
r = r - wold * beta
alpha = matrixmultiply(v, r)
avals.append(alpha)
r = r - w * alpha
if doS:
q = solve(S, r)
else:
q = r
beta = sqrt(matrixmultiply(q, r))
bvals.append(beta)
wold = w
E, V = eigh(tridiagmat(avals, bvals))
return min(E), max(E)
def getF(self, F, D):
n, m = F.shape
err = matrixmultiply(F, matrixmultiply(D, self.S)) - matrixmultiply(self.S, matrixmultiply(D, F))
err = ravel(err)
maxerr = max(abs(err))
self.maxerr = maxerr
if maxerr < self.errcutoff and not self.started:
if VERBOSE:
print "Starting DIIS: Max Err = ", maxerr
self.started = 1
if not self.started:
# Do simple averaging until DIIS starts
if self.Fold != None:
Freturn = 0.5 * F + 0.5 * self.Fold
self.Fold = F
else:
self.Fold = F
Freturn = F
return Freturn
self.Fs.append(F)
self.Errs.append(err)
nit = len(self.Errs)
a = zeros((nit + 1, nit + 1), "d")
b = zeros(nit + 1, "d")
for i in range(nit):
for j in range(nit):
a[i, j] = dot(self.Errs[i], self.Errs[j])
for i in range(nit):
a[nit, i] = a[i, nit] = -1.0
b[i] = 0
# mtx2file(a,'A%d.dat' % nit)
a[nit, nit] = 0
b[nit] = -1.0
# The try loop makes this a bit more stable.
# Thanks to John Kendrick!
try:
c = solve(a, b)
except:
self.Fold = F
return F
F = zeros((n, m), "d")
for i in range(nit):
F += c[i] * self.Fs[i]
return F
def getF(self, F, D):
n, m = F.shape
err = matrixmultiply(F,matrixmultiply(D,self.S)) -\
matrixmultiply(self.S,matrixmultiply(D,F))
err = ravel(err)
maxerr = max(abs(err))
self.maxerr = maxerr
if maxerr < self.errcutoff and not self.started:
if VERBOSE: print "Starting DIIS: Max Err = ", maxerr
self.started = 1
if not self.started:
# Do simple averaging until DIIS starts
if self.Fold != None:
Freturn = 0.5 * F + 0.5 * self.Fold
self.Fold = F
else:
self.Fold = F
Freturn = F
return Freturn
self.Fs.append(F)
self.Errs.append(err)
nit = len(self.Errs)
a = zeros((nit + 1, nit + 1), 'd')
b = zeros(nit + 1, 'd')
for i in xrange(nit):
for j in xrange(nit):
a[i, j] = dot(self.Errs[i], self.Errs[j])
for i in xrange(nit):
a[nit, i] = a[i, nit] = -1.0
b[i] = 0
#mtx2file(a,'A%d.dat' % nit)
a[nit, nit] = 0
b[nit] = -1.0
# The try loop makes this a bit more stable.
# Thanks to John Kendrick!
try:
c = solve(a, b)
except:
self.Fold = F
return F
F = zeros((n, m), 'd')
for i in xrange(nit):
F += c[i] * self.Fs[i]
return F
def getF(self, F, D):
n, m = F.shape
err = matrixmultiply(F, matrixmultiply(D, self.S)) - matrixmultiply(self.S, matrixmultiply(D, F))
err = ravel(err)
maxerr = max(abs(err))
if maxerr < self.errcutoff and not self.started:
if VERBOSE:
print "Starting DIIS: Max Err = ", maxerr
self.started = 1
if not self.started:
# Do simple averaging until DIIS starts
if self.Fold:
Freturn = 0.5 * F + 0.5 * self.Fold
else:
Freturn = F
self.Fold = F
return Freturn
elif not self.errold:
Freturn = 0.5 * F + 0.5 * self.Fold
self.errold = err
return Freturn
a = zeros((3, 3), "d")
b = zeros(3, "d")
a[0, 0] = dot(self.errold, self.errold)
a[1, 0] = dot(self.errold, err)
a[0, 1] = a[1, 0]
a[1, 1] = dot(err, err)
a[:, 2] = -1
a[2, :] = -1
a[2, 2] = 0
b[2] = -1
c = solve(a, b)
# Handle a few special cases:
alpha = c[1]
print alpha, c
# if alpha < 0: alpha = 0
# if alpha > 1: alpha = 1
F = (1 - alpha) * self.Fold + alpha * F
self.errold = err
self.Fold = F
return F
def getF(self, F, D):
n, m = F.shape
err = matrixmultiply(F,matrixmultiply(D,self.S)) -\
matrixmultiply(self.S,matrixmultiply(D,F))
err = ravel(err)
maxerr = max(abs(err))
if maxerr < self.errcutoff and not self.started:
if VERBOSE: print "Starting DIIS: Max Err = ", maxerr
self.started = 1
if not self.started:
# Do simple averaging until DIIS starts
if self.Fold:
Freturn = 0.5 * F + 0.5 * self.Fold
else:
Freturn = F
self.Fold = F
return Freturn
elif not self.errold:
Freturn = 0.5 * F + 0.5 * self.Fold
self.errold = err
return Freturn
a = zeros((3, 3), 'd')
b = zeros(3, 'd')
a[0, 0] = dot(self.errold, self.errold)
a[1, 0] = dot(self.errold, err)
a[0, 1] = a[1, 0]
a[1, 1] = dot(err, err)
a[:, 2] = -1
a[2, :] = -1
a[2, 2] = 0
b[2] = -1
c = solve(a, b)
# Handle a few special cases:
alpha = c[1]
print alpha, c
#if alpha < 0: alpha = 0
#if alpha > 1: alpha = 1
F = (1 - alpha) * self.Fold + alpha * F
self.errold = err
self.Fold = F
return F
def oep_uhf_an(atoms,orbsa,orbsb,**opts):
"""oep_hf - Form the optimized effective potential for HF exchange.
Implementation of Wu and Yang's Approximate Newton Scheme
from J. Theor. Comp. Chem. 2, 627 (2003).
oep_uhf(atoms,orbs,**opts)
atoms A Molecule object containing a list of the atoms
orbs A matrix of guess orbitals
Options
-------
bfs None The basis functions to use for the wfn
pbfs None The basis functions to use for the pot
basis_data None The basis data to use to construct bfs
integrals None The one- and two-electron integrals to use
If not None, S,h,Ints
"""
maxiter = opts.get('maxiter',100)
tol = opts.get('tol',1e-5)
ETemp = opts.get('ETemp',False)
bfs = opts.get('bfs',None)
if not bfs:
basis = opts.get('basis',None)
bfs = getbasis(atoms,basis)
# The basis set for the potential can be set different from
# that used for the wave function
pbfs = opts.get('pbfs',None)
if not pbfs: pbfs = bfs
npbf = len(pbfs)
integrals = opts.get('integrals',None)
if integrals:
S,h,Ints = integrals
else:
S,h,Ints = getints(bfs,atoms)
nel = atoms.get_nel()
nclosed,nopen = atoms.get_closedopen()
nalpha,nbeta = nclosed+nopen,nclosed
Enuke = atoms.get_enuke()
# Form the OEP using Yang/Wu, PRL 89 143002 (2002)
nbf = len(bfs)
norb = nbf
ba = zeros(npbf,'d')
bb = zeros(npbf,'d')
# Form and store all of the three-center integrals
# we're going to need.
# These are <ibf|gbf|jbf> (where 'bf' indicates basis func,
# as opposed to MO)
# N^3 storage -- obviously you don't want to do this for
# very large systems
Gij = []
for g in range(npbf):
gmat = zeros((nbf,nbf),'d')
Gij.append(gmat)
gbf = pbfs[g]
for i in range(nbf):
ibf = bfs[i]
for j in range(i+1):
jbf = bfs[j]
gij = three_center(ibf,gbf,jbf)
gmat[i,j] = gij
gmat[j,i] = gij
# Compute the Fermi-Amaldi potential based on the LDA density.
# We're going to form this matrix from the Coulombic matrix that
# arises from the input orbitals. D0 and J0 refer to the density
# matrix and corresponding Coulomb matrix
D0 = mkdens(orbsa,0,nalpha)+mkdens(orbsb,0,nbeta)
J0 = getJ(Ints,D0)
Vfa = ((nel-1.)/nel)*J0
H0 = h + Vfa
eold = 0
for iter in range(maxiter):
Hoepa = get_Hoep(ba,H0,Gij)
Hoepb = get_Hoep(ba,H0,Gij)
orbea,orbsa = geigh(Hoepa,S)
orbeb,orbsb = geigh(Hoepb,S)
if ETemp:
efermia = get_efermi(2*nalpha,orbea,ETemp)
occsa = get_fermi_occs(efermia,orbea,ETemp)
Da = mkdens_occs(orbsa,occsa)
efermib = get_efermi(2*nbeta,orbeb,ETemp)
occsb = get_fermi_occs(efermib,orbeb,ETemp)
Db = mkdens_occs(orbsb,occsb)
entropy = 0.5*(get_entropy(occsa,ETemp)+get_entropy(occsb,ETemp))
else:
Da = mkdens(orbsa,0,nalpha)
Db = mkdens(orbsb,0,nbeta)
J = getJ(Ints,Da) + getJ(Ints,Db)
Ka = getK(Ints,Da)
Kb = getK(Ints,Db)
energy = (trace2(2*h+J-Ka,Da)+trace2(2*h+J-Kb,Db))/2\
+Enuke
if ETemp: energy += entropy
if abs(energy-eold) < tol:
break
else:
eold = energy
logging.debug("OEP AN Opt: %d %f" % (iter,energy))
# Do alpha and beta separately
# Alphas
dV_ao = J-Ka-Vfa
dV = matrixmultiply(orbsa,matrixmultiply(dV_ao,transpose(orbsa)))
X = zeros((nbf,nbf),'d')
c = zeros(nbf,'d')
for k in range(nbf):
Gk = matrixmultiply(orbsa,matrixmultiply(Gij[k],
transpose(orbsa)))
for i in range(nalpha):
for a in range(nalpha,norb):
c[k] += dV[i,a]*Gk[i,a]/(orbea[i]-orbea[a])
for l in range(nbf):
Gl = matrixmultiply(orbsa,matrixmultiply(Gij[l],
transpose(orbsa)))
for i in range(nalpha):
for a in range(nalpha,norb):
X[k,l] += Gk[i,a]*Gl[i,a]/(orbea[i]-orbea[a])
# This should actually be a pseudoinverse...
ba = solve(X,c)
# Betas
dV_ao = J-Kb-Vfa
dV = matrixmultiply(orbsb,matrixmultiply(dV_ao,transpose(orbsb)))
X = zeros((nbf,nbf),'d')
c = zeros(nbf,'d')
for k in range(nbf):
Gk = matrixmultiply(orbsb,matrixmultiply(Gij[k],
transpose(orbsb)))
for i in range(nbeta):
for a in range(nbeta,norb):
c[k] += dV[i,a]*Gk[i,a]/(orbeb[i]-orbeb[a])
for l in range(nbf):
Gl = matrixmultiply(orbsb,matrixmultiply(Gij[l],
transpose(orbsb)))
for i in range(nbeta):
for a in range(nbeta,norb):
X[k,l] += Gk[i,a]*Gl[i,a]/(orbeb[i]-orbeb[a])
# This should actually be a pseudoinverse...
bb = solve(X,c)
logging.info("Final OEP energy = %f" % energy)
return energy,(orbea,orbeb),(orbsa,orbsb)
def oep_hf_an(atoms,orbs,**opts):
"""oep_hf - Form the optimized effective potential for HF exchange.
Implementation of Wu and Yang's Approximate Newton Scheme
from J. Theor. Comp. Chem. 2, 627 (2003).
oep_hf(atoms,orbs,**opts)
atoms A Molecule object containing a list of the atoms
orbs A matrix of guess orbitals
Options
-------
bfs None The basis functions to use for the wfn
pbfs None The basis functions to use for the pot
basis_data None The basis data to use to construct bfs
integrals None The one- and two-electron integrals to use
If not None, S,h,Ints
"""
maxiter = opts.get('maxiter',100)
tol = opts.get('tol',1e-5)
bfs = opts.get('bfs',None)
if not bfs:
basis = opts.get('basis',None)
bfs = getbasis(atoms,basis)
# The basis set for the potential can be set different from
# that used for the wave function
pbfs = opts.get('pbfs',None)
if not pbfs: pbfs = bfs
npbf = len(pbfs)
integrals = opts.get('integrals',None)
if integrals:
S,h,Ints = integrals
else:
S,h,Ints = getints(bfs,atoms)
nel = atoms.get_nel()
nocc,nopen = atoms.get_closedopen()
Enuke = atoms.get_enuke()
# Form the OEP using Yang/Wu, PRL 89 143002 (2002)
nbf = len(bfs)
norb = nbf
bp = zeros(nbf,'d')
bvec = opts.get('bvec',None)
if bvec:
assert len(bvec) == npbf
b = array(bvec)
else:
b = zeros(npbf,'d')
# Form and store all of the three-center integrals
# we're going to need.
# These are <ibf|gbf|jbf> (where 'bf' indicates basis func,
# as opposed to MO)
# N^3 storage -- obviously you don't want to do this for
# very large systems
Gij = []
for g in range(npbf):
gmat = zeros((nbf,nbf),'d')
Gij.append(gmat)
gbf = pbfs[g]
for i in range(nbf):
ibf = bfs[i]
for j in range(i+1):
jbf = bfs[j]
gij = three_center(ibf,gbf,jbf)
gmat[i,j] = gij
gmat[j,i] = gij
# Compute the Fermi-Amaldi potential based on the LDA density.
# We're going to form this matrix from the Coulombic matrix that
# arises from the input orbitals. D0 and J0 refer to the density
# matrix and corresponding Coulomb matrix
D0 = mkdens(orbs,0,nocc)
J0 = getJ(Ints,D0)
Vfa = (2*(nel-1.)/nel)*J0
H0 = h + Vfa
b = zeros(nbf,'d')
eold = 0
for iter in range(maxiter):
Hoep = get_Hoep(b,H0,Gij)
orbe,orbs = geigh(Hoep,S)
D = mkdens(orbs,0,nocc)
Vhf = get2JmK(Ints,D)
energy = trace2(2*h+Vhf,D)+Enuke
if abs(energy-eold) < tol:
break
else:
eold = energy
logging.debug("OEP AN Opt: %d %f" % (iter,energy))
dV_ao = Vhf-Vfa
dV = matrixmultiply(transpose(orbs),matrixmultiply(dV_ao,orbs))
X = zeros((nbf,nbf),'d')
c = zeros(nbf,'d')
Gkt = zeros((nbf,nbf),'d')
for k in range(nbf):
# This didn't work; in fact, it made things worse:
Gk = matrixmultiply(transpose(orbs),matrixmultiply(Gij[k],orbs))
for i in range(nocc):
for a in range(nocc,norb):
c[k] += dV[i,a]*Gk[i,a]/(orbe[i]-orbe[a])
for l in range(nbf):
Gl = matrixmultiply(transpose(orbs),matrixmultiply(Gij[l],orbs))
for i in range(nocc):
for a in range(nocc,norb):
X[k,l] += Gk[i,a]*Gl[i,a]/(orbe[i]-orbe[a])
# This should actually be a pseudoinverse...
b = solve(X,c)
logging.info("Final OEP energy = %f" % energy)
return energy,orbe,orbs
def oep_uhf_an(atoms, orbsa, orbsb, **opts):
"""oep_hf - Form the optimized effective potential for HF exchange.
Implementation of Wu and Yang's Approximate Newton Scheme
from J. Theor. Comp. Chem. 2, 627 (2003).
oep_uhf(atoms,orbs,**opts)
atoms A Molecule object containing a list of the atoms
orbs A matrix of guess orbitals
Options
-------
bfs None The basis functions to use for the wfn
pbfs None The basis functions to use for the pot
basis_data None The basis data to use to construct bfs
integrals None The one- and two-electron integrals to use
If not None, S,h,Ints
"""
maxiter = opts.get('maxiter', 100)
tol = opts.get('tol', 1e-5)
ETemp = opts.get('ETemp', False)
bfs = opts.get('bfs', None)
if not bfs:
basis = opts.get('basis', None)
bfs = getbasis(atoms, basis)
# The basis set for the potential can be set different from
# that used for the wave function
pbfs = opts.get('pbfs', None)
if not pbfs: pbfs = bfs
npbf = len(pbfs)
integrals = opts.get('integrals', None)
if integrals:
S, h, Ints = integrals
else:
S, h, Ints = getints(bfs, atoms)
nel = atoms.get_nel()
nclosed, nopen = atoms.get_closedopen()
nalpha, nbeta = nclosed + nopen, nclosed
Enuke = atoms.get_enuke()
# Form the OEP using Yang/Wu, PRL 89 143002 (2002)
nbf = len(bfs)
norb = nbf
ba = zeros(npbf, 'd')
bb = zeros(npbf, 'd')
# Form and store all of the three-center integrals
# we're going to need.
# These are <ibf|gbf|jbf> (where 'bf' indicates basis func,
# as opposed to MO)
# N^3 storage -- obviously you don't want to do this for
# very large systems
Gij = []
for g in xrange(npbf):
gmat = zeros((nbf, nbf), 'd')
Gij.append(gmat)
gbf = pbfs[g]
for i in xrange(nbf):
ibf = bfs[i]
for j in xrange(i + 1):
jbf = bfs[j]
gij = three_center(ibf, gbf, jbf)
gmat[i, j] = gij
gmat[j, i] = gij
# Compute the Fermi-Amaldi potential based on the LDA density.
# We're going to form this matrix from the Coulombic matrix that
# arises from the input orbitals. D0 and J0 refer to the density
# matrix and corresponding Coulomb matrix
D0 = mkdens(orbsa, 0, nalpha) + mkdens(orbsb, 0, nbeta)
J0 = getJ(Ints, D0)
Vfa = ((nel - 1.) / nel) * J0
H0 = h + Vfa
eold = 0
for iter in xrange(maxiter):
Hoepa = get_Hoep(ba, H0, Gij)
Hoepb = get_Hoep(ba, H0, Gij)
orbea, orbsa = geigh(Hoepa, S)
orbeb, orbsb = geigh(Hoepb, S)
if ETemp:
efermia = get_efermi(2 * nalpha, orbea, ETemp)
occsa = get_fermi_occs(efermia, orbea, ETemp)
Da = mkdens_occs(orbsa, occsa)
efermib = get_efermi(2 * nbeta, orbeb, ETemp)
occsb = get_fermi_occs(efermib, orbeb, ETemp)
Db = mkdens_occs(orbsb, occsb)
entropy = 0.5 * (get_entropy(occsa, ETemp) +
get_entropy(occsb, ETemp))
else:
Da = mkdens(orbsa, 0, nalpha)
Db = mkdens(orbsb, 0, nbeta)
J = getJ(Ints, Da) + getJ(Ints, Db)
Ka = getK(Ints, Da)
Kb = getK(Ints, Db)
energy = (trace2(2*h+J-Ka,Da)+trace2(2*h+J-Kb,Db))/2\
+Enuke
if ETemp: energy += entropy
if abs(energy - eold) < tol:
break
else:
eold = energy
logging.debug("OEP AN Opt: %d %f" % (iter, energy))
# Do alpha and beta separately
# Alphas
dV_ao = J - Ka - Vfa
dV = matrixmultiply(orbsa, matrixmultiply(dV_ao, transpose(orbsa)))
X = zeros((nbf, nbf), 'd')
c = zeros(nbf, 'd')
for k in xrange(nbf):
Gk = matrixmultiply(orbsa, matrixmultiply(Gij[k],
transpose(orbsa)))
for i in xrange(nalpha):
for a in xrange(nalpha, norb):
c[k] += dV[i, a] * Gk[i, a] / (orbea[i] - orbea[a])
for l in xrange(nbf):
Gl = matrixmultiply(orbsa,
matrixmultiply(Gij[l], transpose(orbsa)))
for i in xrange(nalpha):
for a in xrange(nalpha, norb):
X[k, l] += Gk[i, a] * Gl[i, a] / (orbea[i] - orbea[a])
# This should actually be a pseudoinverse...
ba = solve(X, c)
# Betas
dV_ao = J - Kb - Vfa
dV = matrixmultiply(orbsb, matrixmultiply(dV_ao, transpose(orbsb)))
X = zeros((nbf, nbf), 'd')
c = zeros(nbf, 'd')
for k in xrange(nbf):
Gk = matrixmultiply(orbsb, matrixmultiply(Gij[k],
transpose(orbsb)))
for i in xrange(nbeta):
for a in xrange(nbeta, norb):
c[k] += dV[i, a] * Gk[i, a] / (orbeb[i] - orbeb[a])
for l in xrange(nbf):
Gl = matrixmultiply(orbsb,
matrixmultiply(Gij[l], transpose(orbsb)))
for i in xrange(nbeta):
for a in xrange(nbeta, norb):
X[k, l] += Gk[i, a] * Gl[i, a] / (orbeb[i] - orbeb[a])
# This should actually be a pseudoinverse...
bb = solve(X, c)
logger.info("Final OEP energy = %f" % energy)
return energy, (orbea, orbeb), (orbsa, orbsb)
def oep_hf_an(atoms, orbs, **opts):
"""oep_hf - Form the optimized effective potential for HF exchange.
Implementation of Wu and Yang's Approximate Newton Scheme
from J. Theor. Comp. Chem. 2, 627 (2003).
oep_hf(atoms,orbs,**opts)
atoms A Molecule object containing a list of the atoms
orbs A matrix of guess orbitals
Options
-------
bfs None The basis functions to use for the wfn
pbfs None The basis functions to use for the pot
basis_data None The basis data to use to construct bfs
integrals None The one- and two-electron integrals to use
If not None, S,h,Ints
"""
maxiter = opts.get('maxiter', 100)
tol = opts.get('tol', 1e-5)
bfs = opts.get('bfs', None)
if not bfs:
basis = opts.get('basis', None)
bfs = getbasis(atoms, basis)
# The basis set for the potential can be set different from
# that used for the wave function
pbfs = opts.get('pbfs', None)
if not pbfs: pbfs = bfs
npbf = len(pbfs)
integrals = opts.get('integrals', None)
if integrals:
S, h, Ints = integrals
else:
S, h, Ints = getints(bfs, atoms)
nel = atoms.get_nel()
nocc, nopen = atoms.get_closedopen()
Enuke = atoms.get_enuke()
# Form the OEP using Yang/Wu, PRL 89 143002 (2002)
nbf = len(bfs)
norb = nbf
bp = zeros(nbf, 'd')
bvec = opts.get('bvec', None)
if bvec:
assert len(bvec) == npbf
b = array(bvec)
else:
b = zeros(npbf, 'd')
# Form and store all of the three-center integrals
# we're going to need.
# These are <ibf|gbf|jbf> (where 'bf' indicates basis func,
# as opposed to MO)
# N^3 storage -- obviously you don't want to do this for
# very large systems
Gij = []
for g in xrange(npbf):
gmat = zeros((nbf, nbf), 'd')
Gij.append(gmat)
gbf = pbfs[g]
for i in xrange(nbf):
ibf = bfs[i]
for j in xrange(i + 1):
jbf = bfs[j]
gij = three_center(ibf, gbf, jbf)
gmat[i, j] = gij
gmat[j, i] = gij
# Compute the Fermi-Amaldi potential based on the LDA density.
# We're going to form this matrix from the Coulombic matrix that
# arises from the input orbitals. D0 and J0 refer to the density
# matrix and corresponding Coulomb matrix
D0 = mkdens(orbs, 0, nocc)
J0 = getJ(Ints, D0)
Vfa = (2 * (nel - 1.) / nel) * J0
H0 = h + Vfa
b = zeros(nbf, 'd')
eold = 0
for iter in xrange(maxiter):
Hoep = get_Hoep(b, H0, Gij)
orbe, orbs = geigh(Hoep, S)
D = mkdens(orbs, 0, nocc)
Vhf = get2JmK(Ints, D)
energy = trace2(2 * h + Vhf, D) + Enuke
if abs(energy - eold) < tol:
break
else:
eold = energy
logging.debug("OEP AN Opt: %d %f" % (iter, energy))
dV_ao = Vhf - Vfa
dV = matrixmultiply(transpose(orbs), matrixmultiply(dV_ao, orbs))
X = zeros((nbf, nbf), 'd')
c = zeros(nbf, 'd')
Gkt = zeros((nbf, nbf), 'd')
for k in xrange(nbf):
# This didn't work; in fact, it made things worse:
Gk = matrixmultiply(transpose(orbs), matrixmultiply(Gij[k], orbs))
for i in xrange(nocc):
for a in xrange(nocc, norb):
c[k] += dV[i, a] * Gk[i, a] / (orbe[i] - orbe[a])
for l in xrange(nbf):
Gl = matrixmultiply(transpose(orbs),
matrixmultiply(Gij[l], orbs))
for i in xrange(nocc):
for a in xrange(nocc, norb):
X[k, l] += Gk[i, a] * Gl[i, a] / (orbe[i] - orbe[a])
# This should actually be a pseudoinverse...
b = solve(X, c)
logger.info("Final OEP energy = %f" % energy)
return energy, orbe, orbs