def test_names(testdir):
"""Test different gs vs excited name. Tests also default names."""
# do a Vibrations calculation first
atoms = H2Morse()
vib = Vibrations(atoms)
vib.run()
assert '0x-' in vib.cache
# do a Resonant Raman calculation
rmc = ResonantRamanCalculator(atoms,
H2MorseExcitedStatesCalculator,
verbose=True)
rmc.run()
# excitation files should reside in the same directory as cache files
assert (Path(rmc.name) / ('ex.eq' + rmc.exext)).is_file()
# XXX does this still make sense?
# remove the corresponding pickle file,
# then Placzek can not anymore use it for vibrational properties
key = '0x-'
assert key in rmc.cache
del rmc.cache[key] # make sure this is not used
om = 1
gam = 0.1
pz = Placzek(atoms, H2MorseExcitedStates, name='vib', exname='raman')
pzi = pz.get_absolute_intensities(omega=om, gamma=gam)[-1]
parprint(pzi, 'Placzek')
# check that work was distributed correctly
assert len(pz.myindices) <= -(-6 // world.size)
def hse_spinorbit(base_dir="./"):
hse_file = os.path.join(base_dir, "hse.gpw")
hse_nowfs_file = os.path.join(base_dir, "hse_nowfs.gpw")
hse_eigen_file = os.path.join(base_dir, "hse_eigenvalues.npz")
hse_eigen_soc_file = os.path.join(base_dir, 'hse_eigenvalues_soc.npz')
if not os.path.isfile(hse_eigen_file):
return
if not os.path.isfile(hse_eigen_file):
return
ranks = [0]
comm = mpi.world.new_communicator(ranks)
if mpi.world.rank in ranks:
calc = GPAW(hse_nowfs_file, communicator=comm, txt=None)
with open(hse_eigen_file, 'rb') as fd:
dct = dict(np.load(fd))
e_skn = dct.get('e_hse_skn')
dct = {}
e_mk, s_kvm = get_soc_eigs(calc,
gw_kn=e_skn,
return_spin=True,
bands=np.arange(e_skn.shape[2]))
dct['e_hse_mk'] = e_mk
dct['s_hse_mk'] = s_kvm[:, 2, :].transpose()
with open(hse_eigen_soc_file, 'wb') as fd:
np.savez(fd, **dct)
parprint("SOC HSE06 finished!")
def elph_do_raman_spectra(calc, supercell, laser_freqs, do_permutations, laser_broadening, phonon_broadening, shift_step, polarizations, write_mode_intensities):
from ase.units import _hplanck, _c, J
parprint('Computing phonons')
ph = ase.phonons.Phonons(atoms=calc.atoms, name="phonons", supercell=supercell)
ph.read()
w_ph = np.array(ph.band_structure([[0, 0, 0]])[0])
if calc.world.rank == 0:
np.save('frequencies.npy', w_ph * 8065.544) # frequencies in cm-1
# And the Raman spectra are calculated
for laser_nm in laser_freqs:
w_l = _hplanck*_c*J/(laser_nm*10**(-9))
for polarization in polarizations:
if len(polarization) != 2:
raise ValueError(f'invalid polarization "{polarization}", should be two characters like "xy"')
d_i = 'xyz'.index(polarization[0])
d_o = 'xyz'.index(polarization[1])
name = "{}nm-{}".format(laser_nm, polarization)
if not os.path.isfile(f"RI_{name}.npy"):
leffers.calculate_raman(
calc=calc, w_ph=w_ph, permutations=do_permutations,
w_l=w_l, ramanname=name, d_i=d_i, d_o=d_o,
gamma_l=laser_broadening, phonon_sigma=phonon_broadening,
shift_step=shift_step, write_mode_intensities=write_mode_intensities,
)
#And plotted
leffers.plot_raman(relative = True, figname = f"Raman_{name}.png", ramanname = name)
def __init__(self,
atoms,
propertyfunction,
save=False,
name='fd',
ending='',
d=0.001,
parallel=0,
world=None):
self.atoms = atoms
self.indices = np.asarray(range(len(atoms)))
self.propertyfunction = propertyfunction
self.save = save
self.name = name
self.ending = ending
self.d = d
self.value = np.empty([len(self.atoms), 3])
if world is None:
world = mpi.world
self.world = world
if world.size < 2:
if parallel > 1:
parprint('#', (self.__class__.__name__ + ':'),
'Serial calculation, keyword parallel ignored.')
parallel = 0
self.parallel = parallel
if parallel > 1:
self.set_parallel()
def get_mode_raman(outpath, eigendata, cart_pol_derivs):
if os.path.exists(outpath):
parprint(f'Found existing {outpath}')
return
world.barrier()
parprint(f'Computing mode raman tensors... ({outpath})')
cart_pol_derivs = np.load('raman-cart.npy')
mode_pol_derivs = []
for row in eigendata['eigenvectors']:
mode_displacements = eigendata['atom_masses'].repeat(3) ** -0.5 * row
mode_displacements /= np.linalg.norm(mode_displacements)
# ∂α_ij ∂α_ij ∂x_ak
# ----- = sum ( ----- ----- )
# ∂u_n a,k ∂x_ak ∂u_n
#
# = dot product of (3n-dimensional gradient of ∂α_ij)
# with (3n-dimensional displacement vector of mode n)
mode_pol_deriv = np.dot(
# move i and j (axes 2 and 3) to the outside and combine axes 0 and 1 (x components)
cart_pol_derivs.transpose((2, 3, 0, 1)).reshape((9, -1)),
mode_displacements,
).reshape((3, 3))
mode_pol_derivs.append(mode_pol_deriv)
np.save(outpath, mode_pol_derivs)
def main(
name,
# root="../ZnVO/",
root="/cluster/scratch/ttian/ZnVO",
clean=False):
if name not in ("Zn", "Co"):
return False
# Directory
if rank == 0:
base_dir = os.path.join(root, "{}V2O5".format(name))
if clean:
shutil.rmtree(base_dir, ignore_errors=True)
if not os.path.exists(base_dir):
os.makedirs(base_dir)
world.barrier()
if clean:
return # on all ranks
atoms = get_structure(name)
parprint(atoms)
base_dir = os.path.join(root, "{}V2O5".format(name))
relax(atoms, name=name, base_dir=base_dir)
return 0
def elph_do_symmetry_expansion(supercell, calc, displacement_dist, phonon, disp_carts, disp_sites, supercell_atoms):
from gpaw.elph.electronphonon import ElectronPhononCoupling
natoms_prim = len(calc.get_atoms())
disp_values = [read_elph_input(f'sym-{index}') for index in range(len(disp_sites))]
# NOTE: phonon.symmetry includes pure translational symmetries of the supercell
# so we use an empty quotient group
quotient_perms = np.array([np.arange(len(supercell_atoms))])
super_lattice = supercell_atoms.get_cell()[...]
super_symmetry = phonon.symmetry.get_symmetry_operations()
oper_sfrac_rots = super_symmetry['rotations']
oper_sfrac_trans = super_symmetry['translations']
oper_cart_rots = np.array([super_lattice.T @ Rfrac @ np.linalg.inv(super_lattice).T for Rfrac in oper_sfrac_rots])
oper_cart_trans = oper_sfrac_trans @ super_lattice
oper_phonopy_coperms = phonon.symmetry.get_atomic_permutations()
oper_phonopy_deperms = np.argsort(oper_phonopy_coperms, axis=1)
# Convert permutations by composing the following three permutations: into phonopy order, apply oper, back to ase order
parprint('phonopy deperms:', oper_phonopy_deperms.shape)
deperm_phonopy_to_ase = interop.get_deperm_from_phonopy_sc_to_ase_sc(natoms_prim, supercell)
oper_deperms = [np.argsort(deperm_phonopy_to_ase)[deperm][deperm_phonopy_to_ase] for deperm in oper_phonopy_deperms]
del oper_phonopy_coperms, oper_phonopy_deperms
elphsym = symmetry.ElphGpawSymmetrySource.from_setups_and_ops(
setups=supercell_atoms.calc.wfs.setups,
lattice=super_lattice,
oper_cart_rots=oper_cart_rots,
oper_cart_trans=oper_cart_trans,
oper_deperms=oper_deperms,
)
if world.rank == 0:
full_derivatives = symmetry.expand_derivs_by_symmetry(
disp_sites, # disp -> atom
disp_carts, # disp -> 3-vec
disp_values, # disp -> T (displaced value, optionally minus equilibrium value)
elph_callbacks_2(supercell_atoms.calc.wfs, elphsym, supercell=supercell), # how to work with T
oper_cart_rots, # oper -> 3x3
oper_perms=oper_deperms, # oper -> atom' -> atom
quotient_perms=quotient_perms,
)
# NOTE: confusingly, Elph wants primitive atoms, but a calc for the supercell
elph = ElectronPhononCoupling(calc.atoms, calc=supercell_atoms.calc, supercell=supercell)
displaced_cell_index = elph.offset
del elph # that's all we needed it for
eq_Vt, eq_dH, eq_forces = read_elph_input('eq')
for a in range(natoms_prim):
for c in range(3):
delta_Vt, delta_dH, delta_forces = full_derivatives[natoms_prim * displaced_cell_index + a][c]
for sign in [-1, +1]:
disp = interop.AseDisplacement(atom=a, axis=c, sign=sign)
disp_Vt = eq_Vt + sign * displacement_dist * delta_Vt
disp_dH = {k: eq_dH[k] + sign * displacement_dist * delta_dH[k] for k in eq_dH}
disp_forces = eq_forces + sign * displacement_dist * delta_forces
pickle.dump(disp_forces, paropen(f'phonons.{disp}.pckl', 'wb'), protocol=2)
pickle.dump((disp_Vt, disp_dH), paropen(f'elph.{disp}.pckl', 'wb'), protocol=2)
world.barrier()
def getBulkEnergy(latticeParams, jobID):
"""
For a given set of bravais lattice parameters, optimize atomic coordinates and return minimum energy
"""
### INITIALIZE
jobObject, bulkObject, calcObject, dft, preCalcObject, preCalcObject, existsPrecalc, atoms, magmoms = initialize(
jobID, latticeParams)
### PRECALCULATE
if existsPrecalc:
optimizePos(atoms,
dft,
preCalcObject,
magmoms,
restart=False,
saveWF=True)
### CALCULATE
optimizePos(atoms,
dft,
calcObject,
magmoms,
restart=existsPrecalc,
saveWF=False)
### GET ENERGY
energy = atoms.get_potential_energy()
with paropen('lattice_opt.log', 'a') as logfile:
logfile.write('%s\t%s\n' % (energy, latticeParams))
parprint('%s\t%s\n' % (energy, latticeParams))
return energy
def get_ensemble_energies(self,
size: int = 2000,
seed: int = 0) -> np.ndarray:
"""Returns an array of ensemble total energies"""
self.seed = seed
if self.verbose:
parprint(self.beef_type, 'ensemble started')
if self.contribs is None:
self.contribs = self.calc.get_nonselfconsistent_energies(
self.beef_type)
self.e = self.calc.get_potential_energy(self.atoms)
if self.beef_type == 'beefvdw':
assert len(self.contribs) == 32
coefs = self.get_beefvdw_ensemble_coefs(size, seed)
elif self.beef_type == 'mbeef':
assert len(self.contribs) == 64
coefs = self.get_mbeef_ensemble_coefs(size, seed)
elif self.beef_type == 'mbeefvdw':
assert len(self.contribs) == 28
coefs = self.get_mbeefvdw_ensemble_coefs(size, seed)
self.de = np.dot(coefs, self.contribs)
self.done = True
if self.verbose:
parprint(self.beef_type, 'ensemble finished')
return self.e + self.de
def get_nmse_structure(self, structure_numbers):
"""
Read cif files from NMSE database directory, return lists of ASE Atoms objects and names
:param structure_numbers: list of NMSE database index numbers
:return: tuple: list of Atoms objects, list of structure names
"""
nmse_data = pd.read_json(self.db_path + 'nmse_data_frame.json')
# Filter structures in NMSE database
general_filters = ['Error==False', 'is_ordered==True', 'Layers==1.0']
compound_filters = dict(
include=['Pb\d*I'], # include only lead iodide compounds
exclude=['Pb\d*I\d*\D'
]) # exclude any lead iodide mixed halide compounds
dft_database = filter_structures(database=nmse_data,
general_filters=general_filters,
compound_filters=compound_filters)
atoms_list = []
structure_base_name_list = []
for structure_number in structure_numbers:
structure_info = dft_database.query(f'Index=={structure_number}')
structure_file_name = structure_info.loc[structure_info.index[0],
'CIF']
structure_base_name, _ = splitext(structure_file_name)
structure_base_name_list.append(structure_base_name)
parprint('Loading file: ', structure_file_name)
# display(structure_info)
atoms_list.append(load_atoms_from_cif(structure_file_name))
return atoms_list, structure_base_name_list
def gwqeh(mater, n_layers, band_num=3):
bb_file(mater)
parprint("Calculate QP correction for {} with {} layers".format(
mater, n_layers))
assert mater in d_list.keys()
assert n_layers >= 2
structure = ["{}{}".format(int(n_layers), mater)]
distances = [d_list[mater]] * (n_layers - 1)
d0 = d_list[mater]
f_out = os.path.join(data_path, "{}/gwqeh_{}".format(mater, n_layers))
# The GWQEH calculation
calc = GPAW(restart=gs_wfs(mater))
ne = calc.get_number_of_electrons()
nb = int(ne // 2)
bands = (nb - band_num, nb + band_num)
del calc
# Calc GWQEH
qeh_corr = GWQEHCorrection(
calc=es_wfs(mater),
gwfile=g0w0_file(mater),
filename=f_out,
structure=structure,
d=distances,
layer=int(n_layers // 2),
bands=bands,
include_q0=True # Why?
)
qeh_corr.calculate_qp_energies()
# parprint(corr)
qeh_corr.save_state_file()
def test_names():
"""Test different gs vs excited name. Tests also default names."""
# do a Vibrations calculation first
atoms = H2Morse()
Vibrations(atoms).run()
assert os.path.isfile('vib.0x-.pckl')
# do a Resonant Raman calculation
rmc = ResonantRamanCalculator(atoms,
H2MorseExcitedStatesCalculator,
verbose=True)
rmc.run()
# remove the corresponding pickle file,
# then Placzek can not anymore use it for vibrational properties
assert os.path.isfile('raman.0x-.pckl')
os.remove('raman.0x-.pckl') # make sure this is not used
om = 1
gam = 0.1
pz = Placzek(atoms, H2MorseExcitedStates, name='vib', exname='raman')
pzi = pz.get_absolute_intensities(omega=om, gamma=gam)[-1]
parprint(pzi, 'Placzek')
# check that work was distributed correctly
assert len(pz.myindices) <= -(-6 // world.size)
def set_calculator(self, calc=None, nkpts=4096):
""" Sets the calculator and resets the k-points according to the cell
shape """
if calc is None and self.calc is None:
parprint("ERROR: no calculator provided")
return
elif calc is not None:
self.calc = calc
kcell = self.atoms.get_reciprocal_cell()
# Vcell = np.abs(np.dot(kcell[0, :],
# np.cross(kcell[1, :], kcell[2, :])))
k12 = np.cross(kcell[0, :], kcell[1, :])
k23 = np.cross(kcell[1, :], kcell[2, :])
k31 = np.cross(kcell[2, :], kcell[0, :])
n1 = 1. / np.linalg.norm(k23)
n2 = 1. / np.linalg.norm(k31)
n3 = 1. / np.linalg.norm(k12)
tot_kpts = nkpts / self.atoms.get_number_of_atoms()
av_kpts = (tot_kpts / (n1 * n2 * n3))**(1. / 3)
kpts1 = int(round(n1 * av_kpts, 0))
kpts2 = int(round(n2 * av_kpts, 0))
kpts3 = int(round(n3 * av_kpts, 0))
kpts = (np.max((kpts1, 1)), np.max((kpts2, 1)), np.max((kpts3, 1)))
if self.verbosity > 0:
parprint("k-points:", kpts)
self.calc.set(kpts={'size': kpts, 'gamma': True})
self.atoms.set_calculator(calc)
def gap(base_dir="./", mode="gllb"):
curr_dir = os.path.dirname(os.path.abspath(__file__))
param_file = os.path.join(curr_dir, "../parameters.json")
gpw_file = os.path.join(base_dir, "gs.gpw")
gap_res = os.path.join(base_dir, "gap.txt")
# Check is gap calculated
if os.path.exists(gap_res):
parprint("Bandgap calculated, will use gpw directly!")
return 0
# Check if gpw file exists
if not os.path.exists(gpw_file):
raise FileNotFoundError("Structure relaxation not done yet!")
if os.path.exists(param_file):
params = json.load(open(param_file, "r"))
else:
raise FileNotFoundError("no parameter file!")
# The true gllb-sc calculation
calc = GPAW(gpw_file, **params["gap"])
calc.get_potential_energy()
# Now for bg
response = calc.hamiltonian.xc.xcs["RESPONSE"]
response.calculate_delta_xc()
EKs, Dxc = response.calculate_delta_xc_perturbation()
gap = EKs + Dxc
if rank == 0:
print("{:.4f}".format(gap), open(gap_res, "w")) # write answer
return 0
def relax(atoms, name="",
base_dir="./",
smax=2e-4):
curr_dir = os.path.dirname(os.path.abspath(__file__))
param_file = os.path.join(curr_dir, "../parameters.json")
gpw_file = os.path.join(base_dir, "gs.gpw")
if os.path.exists(gpw_file):
parprint("Relaxation already done, will use gpw directly!")
return 0
if os.path.exists(param_file):
params = json.load(open(param_file, "r"))
else:
raise FileNotFoundError("no parameter file!")
# calculation asign
calc = GPAW(**params["relax"])
atoms.set_calculator(calc)
traj_filename = os.path.join(base_dir,
"{}_relax.traj".format(name))
log_filename = os.path.join(base_dir,
"{}_relax.log".format(name))
opt = QuasiNewton(atoms,
trajectory=traj_filename,
logfile=log_filename)
mask = [1, 1, 1, 0, 0, 0] # Relax for bulk
opt.run(fmax=0.01, smax=smax, smask=mask)
# Calculate the ground state
calc.set(**params["gs"])
atoms.get_potential_energy()
calc.write(gpw_file)
def calculate_periodic_correction(self):
G_z = self.G_z
if self.Elp is not None:
return self.Elp
if self.epsilon_GG is None:
self.calculate_epsilon_GG()
Elp = 0.0
for vector in self.G_parallel:
G2 = (np.dot(vector, vector) + G_z * G_z)
rho_G = self.q * np.exp(- G2 * self.sigma ** 2 / 2, dtype=complex)
if self.dimensionality == '2d':
rho_G *= np.exp(1j * self.z0 * G_z)
A_GG = (self.GG * self.epsilon_GG['out-of-plane']
+ np.dot(vector, vector) * self.epsilon_GG['in-plane'])
if np.allclose(vector, 0):
A_GG[0, 0] = 1 # The d.c. potential is poorly defined
V_G = np.linalg.solve(A_GG, rho_G)
if np.allclose(vector, 0):
parprint('Skipping G^2=0 contribution to Elp')
V_G[0] = 0
Elp += (rho_G * V_G).sum()
Elp *= 2.0 * np.pi * Ha / self.Omega
self.Elp = Elp
return Elp
def getBulkEnergy(latticeParams):
"""For a given set of bravais lattice parameters, optimize atomic coordinates and return minimum energy"""
global nIter
nIter += 1
atoms = job.fromParams(latticeParams)
calc = job.calc(restart=True) if existsPrecalc else job.calc()
if existsPrecalc:
preCalc = job.calc(precalc=True)
job.optimizePos(atoms,preCalc,saveWF = True)
if job.dftcode =='gpaw':
atoms,calc = job.gpawRestart()
job.optimizePos(atoms,calc)
energy = atoms.get_potential_energy()
with paropen('lattice_opt.log','a') as logfile:
logfile.write('%s\t%s\n' %(energy,latticeParams))
parprint('%s\t%s\n' %(energy,latticeParams))
if job.dftcode=='gpaw':
atoms.calc.write('inp.gpw', mode='all') #for use in getXCContribs
io.write('out.traj',atoms)
return energy
def main(
name,
# root="../ZnVO/",
root="/cluster/scratch/ttian/ZnVO",
model="A",
clean=False):
if name not in ("Zn", "Co"):
return False
# Directory
if rank == 0:
base_dir = os.path.join(root, "{}V2O5".format(name))
if clean:
shutil.rmtree(base_dir, ignore_errors=True)
if not os.path.exists(base_dir):
os.makedirs(base_dir)
world.barrier()
if clean:
return # on all ranks
base_dir = os.path.join(root, "{}V2O5".format(name))
parprint("Running {} with model type {}".format(name, model))
relax(base_dir=base_dir, model=model)
return 0
def check_diff(g1, g2, gd, txt):
# print rank, txt, "shapes", g1.shape, g2.shape
intd = gd.integrate(np.abs(g1 - g2))
parprint(txt, 'integrated diff=', intd, end='')
maxd = np.max(np.abs(g1 - g2))
parprint('max diff=', maxd)
equal(intd, 0, 1.e-8)
equal(maxd, 0, 1.e-9)
def check_diff(g1, g2, gd, txt):
# print rank, txt, "shapes", g1.shape, g2.shape
intd = gd.integrate(np.abs(g1 - g2))
parprint(txt, "integrated diff=", intd, end="")
maxd = np.max(np.abs(g1 - g2))
parprint("max diff=", maxd)
equal(intd, 0, 1.0e-8)
equal(maxd, 0, 1.0e-9)
def test_single(self):
sb = StructureBuilder()
atoms, *_ = sb.get_structure("Si", "diamond")
base_dir = os.path.join(os.path.dirname(__file__),
"../../tmp/Si-eps-test/")
m_calc = MaterCalc(atoms=atoms, base_dir=base_dir)
# PBE
parprint(m_calc.check_status())
def run_job(label):
cmd = "g09 < {0}.com > {0}.log".format(label)
parprint(cmd)
exit_state = os.system(cmd)
if exit_state == 0:
print("Calculation exited normally")
else:
print("Abnormal job with exit code {0}".format(exit_state))
return exit_state
def print_version(version):
parprint("""
____ _ _
/ ___|__ _| |_| | ___ __ _ _ __ _ __
| | / _` | __| | / _ \/ _` | '__| '_ \
| |__| (_| | |_| |__| __/ (_| | | | | | |
\____\__,_|\__|_____\___|\__,_|_| |_| |_| """ + version + """
""")
def do_structure(supercell_atoms, name):
forces_path = f'phonons.{name}.pckl'
elph_path = f'elph.{name}.pckl'
if not os.path.exists(elph_path):
parprint(f'== computing elph.{name}.pckl')
elph_data = get_elph_data(supercell_atoms)
forces = supercell_atoms.get_forces()
pickle.dump(forces, paropen(forces_path, 'wb'), protocol=2)
pickle.dump(elph_data, paropen(elph_path, 'wb'), protocol=2)
def polarizability(base_dir="./", mode="df", fermi_shift=None):
curr_dir = os.path.dirname(os.path.abspath(__file__))
es_gpw = os.path.join(base_dir, "es.gpw")
param_file = os.path.join(curr_dir, "../parameters.json")
if os.path.exists(param_file):
params = json.load(open(param_file, "r"))
else:
raise FileNotFoundError("no parameter file!")
if not os.path.exists(es_gpw):
raise FileNotFoundError("Excited state not calculated!")
if mode not in ("df", "tetra"):
raise ValueError("Mode should be df or tetra")
if fermi_shift is None:
data_file = os.path.join(base_dir,
"polarizability_{}.npz".format(mode))
else:
data_file = os.path.join(base_dir,
"polarizability_{}_{:.2f}.npz".format(mode, fermi_shift))
params[mode]["intraband"] = True
if os.path.exists(data_file):
parprint("Polarizability file exists!")
return 0
df = DielectricFunction(calc=es_gpw,
**params[mode],
gate_voltage=fermi_shift) # add energy shift
alpha0x, alphax = df.get_polarizability(q_c=[0, 0, 0],
direction="x",
pbc=[True, True, False],
filename=None)
alpha0y, alphay = df.get_polarizability(q_c=[0, 0, 0],
direction="y",
pbc=[True, True, False],
filename=None)
alpha0z, alphaz = df.get_polarizability(q_c=[0, 0, 0],
direction="z",
pbc=[True, True, False],
filename=None)
freq = df.get_frequencies()
data = dict(frequencies=freq,
alpha_x=alphax,
alpha_y=alphay,
alpha_z=alphaz,
alpha_x0=alpha0x,
alpha_y0=alpha0y,
alpha_z0=alpha0z,)
from ase.parallel import world
import numpy
if world.rank == 0:
numpy.savez_compressed(data_file, **data)
def set_atoms(self, structure=None):
""" Sets the atoms from a given ATAT structure file """
if structure is not None:
to_min_tilt = self.parameters.to_min_tilt
to_niggli = self.parameters.to_niggli
self.atoms = read_atat_input(structure,
pbc=(1, 1, 1),
verbosity=self.verbosity,
minimize_tilt=to_min_tilt,
niggli_reduce=to_niggli)
else:
parprint("ERROR: No ATAT structure file given")
def _cleanall(basedir):
parprint("Clean up {0}".format(basedir))
if rank == 0:
p = Path(basedir)
plist = []
for type in ["*.com", "*.log", "*.ase",
"*.xyz", "*.chk", "lsf*"]:
plist = plist + list(p.glob(type))
for f in plist:
if f.name != "init.xyz":
os.unlink(f)
def permittivity(base_dir="./", mode="df"):
curr_dir = os.path.dirname(os.path.abspath(__file__))
es_gpw = os.path.join(base_dir, "es.gpw")
param_file = os.path.join(curr_dir, "../parameters.json")
if os.path.exists(param_file):
params = json.load(open(param_file, "r"))
else:
raise FileNotFoundError("no parameter file!")
if not os.path.exists(es_gpw):
raise FileNotFoundError("Excited state not calculated!")
if mode not in ("df", "tetra"):
raise ValueError("Mode should be df or tetra")
data_file = os.path.join(base_dir, "polarizability_{}.npz".format(mode))
if os.path.exists(data_file):
parprint("Polarizability file exists!")
return 0
df = DielectricFunction(calc=es_gpw, **params[mode])
eps0x, epsx = df.get_dielectric_function(
q_c=[0, 0, 0],
direction="x",
#pbc=[True, True, False],
filename=None)
eps0y, epsy = df.get_dielectric_function(
q_c=[0, 0, 0],
direction="y",
#pbc=[True, True, False],
filename=None)
eps0z, epsz = df.get_dielectric_function(
q_c=[0, 0, 0],
direction="z",
#pbc=[True, True, False],
filename=None)
freq = df.get_frequencies()
data = dict(
frequencies=freq,
eps_x=epsx,
eps_y=epsy,
eps_z=epsz,
eps_x0=eps0x,
eps_y0=eps0y,
eps_z0=eps0z,
)
from ase.parallel import world
import numpy
if world.rank == 0:
numpy.savez_compressed(data_file, **data)
def bb_file(mater):
f_name = os.path.join(os.path.curdir, "{}-chi.npz".format(mater))
if os.path.exists(f_name):
return f_name
else: # Calculate the BB
parprint("Chi matrix not calculated, build for now!")
df = DielectricFunction(calc=es_wfs(mater),
eta=0.1,
intraband=False,
truncation="2D")
bb = BuildingBlock(mater, df, qmax=3)
bb.calculate_building_block()
return f_name
def do_structure(supercell_atoms, name):
with cache.lock(name) as handle:
if handle is not None:
parprint(f'== computing elph/cache.{name}.json')
Vt_sG, dH_all_asp = get_elph_data(supercell_atoms)
forces = supercell_atoms.get_forces()
if world.rank == 0:
handle.write(
ElphDataset(
Vt_sG=Vt_sG,
dH_all_asp=dH_all_asp,
forces=forces,
))
def converged(self):
"""Function that checks the convergence of the min. surrogate model."""
self.list_fmax = get_fmax(np.array([self.list_gradients[-1]]))
self.max_abs_forces = np.max(np.abs(self.list_fmax))
if self.max_abs_forces < self.fmax:
parprint('Congratulations. Structural optimization has converged.')
parprint('All the evaluated structures can be found in:',
self.filename)
print_cite_mlmin()
return True
return False
def print_force_summary(self):
"""Print a detailed summary of forces in the system.
"""
message = []
message.append("Total forces:")
if self.forces is None:
message.append(" Not calculated")
else:
for i, force in enumerate(self.forces):
message.append(" " + str(i) + ": " + str(force))
message.append("")
# Forces in subsystems
for name, subsystem in self.subsystems.iteritems():
message.append("Subsystem \"" + name + "\":")
if subsystem.forces is None:
message.append(" Not calculated")
else:
for i, force in enumerate(subsystem.forces):
message.append(" " + str(i) + ": " + str(force))
message.append("")
# Forces in interactions
for pair, interaction in self.subsystem_interactions.iteritems():
message.append("Interaction forces between \""+pair[0]+"\" and \""+pair[1] + ":")
# Total interaction force
message.append(" Total:")
if interaction.interaction_forces is None:
message.append(" Not calculated")
else:
for i, force in enumerate(interaction.interaction_forces):
message.append(" " + str(i) + ": " + str(force))
message.append("")
# Link atom correction
message.append(" Link atom correction:")
if interaction.link_atom_correction_forces is None:
message.append(" Not calculated")
else:
for i, force in enumerate(interaction.link_atom_correction_forces):
message.append(" " + str(i) + ": " + str(force))
message.append("")
str_message = style_message("HYBRIDCALCULATOR FORCE SUMMARY", message)
parprint(str_message)
def run(lastres=[]):
results = []
# Hirshfeld ----------------------------------------
if 1:
hd = HirshfeldDensity(calc)
# check for the number of electrons
expected = [[None, 10],
[[0, 1, 2], 10],
[[1, 2], 2],
[[0], 8],
]
#expected = [[[0, 2], 9], ]
#expected = [[None, 10], ]
for gridrefinement in [1, 2, 4]:
#Test for all gridrefinements for get_all_electron_density
parprint('grid refinement', gridrefinement)
for result in expected:
indicees, result = result
full, gd = hd.get_density(indicees, gridrefinement)
parprint('indicees', indicees, end=': ')
parprint('result, expected:', gd.integrate(full), result)
if gridrefinement < 4:
#The highest level of gridrefinement gets wrong electron numbers
equal(gd.integrate(full), result, 1.e-8)
else:
equal(gd.integrate(full), result, 1.e-5)
hp = HirshfeldPartitioning(calc)
vr = hp.get_effective_volume_ratios()
parprint('Hirshfeld:', vr)
if len(lastres):
equal(vr, lastres.pop(0), 1.e-10)
results.append(vr)
# Wigner-Seitz ----------------------------------------
if 1:
ws = WignerSeitz(calc.density.finegd, mol, calc)
vr = ws.get_effective_volume_ratios()
parprint('Wigner-Seitz:', vr)
if len(lastres):
equal(vr, lastres.pop(0), 1.e-10)
results.append(vr)
return results
def initialize(self, paw, allocate=True):
BaseInducedField.initialize(self, paw, allocate)
assert hasattr(paw, 'time') and hasattr(paw, 'niter'), 'Use TDDFT!'
self.time = paw.time
self.niter = paw.niter
# TODO: remove this requirement
assert np.count_nonzero(paw.kick_strength) > 0, \
'Apply absorption kick before %s' % self.__class__.__name__
# Background electric field
self.Fbgef_v = paw.kick_strength
# Attach to PAW-type object
paw.attach(self, self.interval)
# TODO: write more details (folding, freqs, etc)
parprint('%s: Attached ' % self.__class__.__name__)
def print_interaction_charge_summary(self):
"""Print a summary of the atomic charges that are used in the
electrostatic interaction between subsystems.
"""
message = []
for name, subsystem in self.subsystems.iteritems():
message.append("Subsystem \"" + name + "\":")
for i_atom, atom in enumerate(subsystem.atoms_for_interaction):
symbol = atom.symbol
charge = atom.charge
message.append(" Number: " + str(i_atom) + ", Symbol: " + symbol + ", Charge: " + str(charge))
message.append("")
str_message = style_message("HYBRIDCALCULATOR SUMMARY OF CHARGES USED IN INTERACTIONS", message)
parprint(str_message)
def update(self):
# Update time
self.time = self.paw.time
time_step = self.paw.time_step
# Complex exponential with envelope
f_w = np.exp(1.0j * self.omega_w * self.time) * \
self.envelope(self.time) * time_step
# Time-dependent quantities
n_G = (-1.0) * self.fdtd.classical_material.charge_density * self.fdtd.classical_material.sign
# Update Fourier transforms
for w in range(self.nw):
self.Fn_wsG[w] += (n_G - self.n0_G) * f_w[w]
# Restart file
if self.restart_file is not None and \
self.niter % self.paw.dump_interval == 0:
self.write(self.restart_file)
parprint('%s: Wrote restart file %s' % (self.__class__.__name__, self.restart_file))
def print_energy_summary(self):
"""Print a detailed summary of the different energies in the system.
This includes the energies in the subsystems, interaction energies and
possible energy corrections.
"""
message = []
message.append("Total energy: "+str(self.potential_energy))
message.append("")
for name, subsystem in self.subsystems.iteritems():
message.append("Subsystem \"" + name + "\":")
if subsystem.potential_energy is None:
ss_energy = "Not calculated"
else:
ss_energy = str(subsystem.potential_energy)
message.append(" Potential energy: " + ss_energy)
message.append("")
for pair, interaction in self.subsystem_interactions.iteritems():
message.append("Interaction between \""+pair[0]+"\" and \""+pair[1] + ":")
# Total interaction energy
if interaction.interaction_energy is None:
b_energy = "Not calculated"
else:
b_energy = str(interaction.interaction_energy)
message.append(" Total interaction energy: "+b_energy)
# Link atom correction energy
if interaction.link_atom_correction_energy is None:
link_atom_correction_energy = "Not calculated"
else:
link_atom_correction_energy = str(interaction.link_atom_correction_energy)
message.append(" Link atom correction energy: "+link_atom_correction_energy)
str_message = style_message("HYBRIDCALCULATOR ENERGY SUMMARY", message)
parprint(str_message)
def update(self):
# Update time
self.time = self.paw.time
time_step = self.paw.time_step
# Complex exponential with envelope
f_w = np.exp(1.0j * self.omega_w * self.time) * \
self.envelope(self.time) * time_step
# Time-dependent quantities
nt_sG = self.density.nt_sG
D_asp = self.density.D_asp
# Update Fourier transforms
for w in range(self.nw):
self.Fnt_wsG[w] += (nt_sG - self.n0t_sG) * f_w[w]
for a, D_sp in D_asp.items():
self.FD_awsp[a][w] += (D_sp - self.D0_asp[a]) * f_w[w]
# Restart file
if self.restart_file is not None and \
self.niter % self.paw.dump_interval == 0:
self.write(self.restart_file)
parprint('%s: Wrote restart file' % self.__class__.__name__)
h = 0.3
s = Cluster(molecule("H2O"))
s.minimal_box(3.0, h)
gpwname = "H2O_h" + str(h) + ".gpw"
try:
# XXX check why this fails in parallel
calc = GPAW(gpwname + "failsinparallel", txt=None)
atoms = calc.get_atoms()
calc.density.set_positions(atoms.get_scaled_positions() % 1.0)
calc.density.interpolate_pseudo_density()
calc.density.calculate_pseudo_charge()
except IOError:
calc = GPAW(h=h, charge=0, txt=None)
calc.calculate(s)
calc.write(gpwname)
dipole_c = calc.get_dipole_moment()
parprint("Dipole", dipole_c)
center = np.array([1, 1, 1]) * 50.0
mp = Multipole(center, calc, lmax=2)
q_L = mp.expand(-calc.density.rhot_g)
parprint("Multipole", q_L)
# The dipole moment is independent of the center
equal(dipole_c[2], q_L[2], 1e-10)
mp.to_file(calc, mode="w")
if 1:
# test ZeroKelvin vs FixedOccupations
c = GPAW(h=h, nbands=nbands,
occupations=ZeroKelvin(True),
convergence=convergence,
txt=txt)
H2.set_calculator(c)
E_zk = H2.get_potential_energy()
c = GPAW(h=h, nbands=nbands,
occupations=FixedOccupations([[2, 0]]),
convergence=convergence,
txt=txt)
H2.set_calculator(c)
E_fo = H2.get_potential_energy()
parprint(E_zk, E_fo)
equal(E_zk, E_fo, 1.e-10)
if 1:
# test spin-paired vs spin-polarized
c = GPAW(h=h, nbands=nbands,
occupations=FixedOccupations([[1,1]]),
convergence=convergence,
txt=txt)
H2.set_calculator(c)
E_ns = H2.get_potential_energy()
if 1:
c = GPAW(h=h, nbands=nbands, spinpol=True,
occupations=FixedOccupations([[0.5, 0.5]] * 2),
convergence=convergence,
txt=txt)
print(np.round(crk.C*10)/10)
# Get parameter used for fitting crack tip position
residual_func = parameter('residual_func', crack.displacement_residual)
_residual_func = residual_func
tip_tol = parameter('tip_tol', 1e-4)
tip_mixing_alpha = parameter('tip_mixing_alpha', 1.0)
write_trajectory_during_optimization = parameter('write_trajectory_during_optimization', False)
# Get Griffith's k1.
k1g = crk.k1g(params.surface_energy)
parprint('Griffith k1 = %f' % k1g)
# Apply initial strain field.
tip_x = parameter('tip_x', cryst.cell.diagonal()[0]/2)
tip_y = parameter('tip_y', cryst.cell.diagonal()[1]/2)
bondlength = parameter('bondlength', 2.7)
a = cryst.copy()
a.set_pbc([False, False, True])
ux, uy = crk.displacements(cryst.positions[:,0], cryst.positions[:,1],
tip_x, tip_y, params.k1*k1g)
a.positions[:ncryst,0] += ux
a.positions[:ncryst,1] += uy
def summary(self, omega, gamma=0.1,
method='standard', direction='central',
intensity_unit='(D/A)2/amu', log=sys.stdout):
"""Print summary for given omega [eV]"""
hnu = self.get_energies(method, direction)
s = 0.01 * units._e / units._c / units._hplanck
intensities = self.get_intensities(omega, gamma)
if isinstance(log, str):
log = paropen(log, 'a')
parprint('-------------------------------------', file=log)
parprint(' excitation at ' + str(omega) + ' eV', file=log)
parprint(' gamma ' + str(gamma) + ' eV\n', file=log)
parprint(' Mode Frequency Intensity', file=log)
parprint(' # meV cm^-1 [a.u.]', file=log)
parprint('-------------------------------------', file=log)
for n, e in enumerate(hnu):
if e.imag != 0:
c = 'i'
e = e.imag
else:
c = ' '
e = e.real
parprint('%3d %6.1f%s %7.1f%s %9.3g' %
(n, 1000 * e, c, s * e, c, intensities[n]),
file=log)
parprint('-------------------------------------', file=log)
parprint('Zero-point energy: %.3f eV' % self.get_zero_point_energy(),
file=log)
from gpaw.response.g0w0 import G0W0
# We start by setting up a G0W0 calculator object
gw = G0W0('Si_gs.gpw', # Path to groundstate gpw file
filename='Si_g0w0_ppa', # filename base for output files
kpts=None, # List of quasiparticle k-point indices
# or None = all k-points
bands=(3, 5), # Range of quasiparticle bands - last
# index is NOT included
ecut=100., # Plane wave basis cut-off energy
ppa=True) # Use Plasmon Pole Approximation
# Perform the GW calculation. The results, ie. quasiparticle energies, as
# well as original Kohn-Sham eigenvalues, occupation numbers, DFT XC and
# self-energy contributions and renormalization factors are returned as a
# python dictionary object
result = gw.calculate()
ks_skn = result['eps'] # Get Kohn-Sham eigenvalues
ks_cbmin = np.amin(ks_skn[0, :, 1]) # DFT conduction band minimum
ks_vbmax = np.amax(ks_skn[0, :, 0]) # DFT valence band maximum
ks_gap = ks_cbmin - ks_vbmax # DFT band gap
qp_skn = result['qp'] # GW quasiparticle energies
qp_cbmin = np.amin(qp_skn[0, :, 1]) # GW conduction band minimum
qp_vbmax = np.amax(qp_skn[0, :, 0]) # GW valence band maximum
qp_gap = qp_cbmin - qp_vbmax # GW band gap
parprint('Kohn-Sham gap = %.3f' % ks_gap)
parprint('G0W0 gap = %.3f' % qp_gap)
cell=(a, a, c))
calc = GPAW(xc='PBE', h=0.25, nbands=3, spinpol=False, txt=txt)
H2.set_calculator(calc)
xc='LDA'
lr = LrTDDFT(calc, xc=xc)
# excited state with forces
accuracy = 0.015
exst = ExcitedState(lr, 0, d=0.01,
parallel=2,
txt=sys.stdout,
)
t0 = time.time()
parprint("########### first call to forces --> calculate")
forces = exst.get_forces(H2)
parprint("time used:", time.time() - t0)
for c in range(2):
equal(forces[0,c], 0.0, accuracy)
equal(forces[1,c], 0.0, accuracy)
equal(forces[0, 2] + forces[1, 2], 0.0, accuracy)
parprint("########### second call to potential energy --> just return")
t0 = time.time()
E = exst.get_potential_energy()
parprint("E=", E)
parprint("time used:", time.time() - t0)
t0 = time.time()
E = exst.get_potential_energy(H2)
def get_induced_density(self, from_density='comp', gridrefinement=2):
paw = self.paw
lr = self.lr
omega_w = self.omega_w
if gridrefinement == 1:
gd = self.gd
elif gridrefinement == 2:
gd = self.density.finegd
else:
raise NotImplementedError
nkss = len(lr.kss)
nexcs = len(lr)
omega_I = np.empty((nexcs), dtype=float)
# C_Iij: weights for each excitation I and KS-pair ij
C_Iij = np.zeros((nexcs, nkss), dtype=float)
# Calculate C_Iij
FIsqfe_ij = np.zeros((nkss), dtype=float)
for I, exc in enumerate(lr):
omega_I[I] = exc.energy
B = 0.0
for ij, ks in enumerate(lr.kss):
FIsqfe_ij[ij] = exc.f[ij] * np.sqrt(ks.fij * ks.energy)
B += ks.mur[self.kickdir] * FIsqfe_ij[ij]
C_Iij[I] = 2 * B * FIsqfe_ij
# Fold C_Iij to C_wij
# C_wij: weights for each requested frequency w and KS-pair ij
self.omega_w, C_wij = self.folder.fold_values(omega_I, C_Iij, omega_w)
assert (self.omega_w == omega_w).all() # TODO: remove
Fn_wg = gd.zeros((self.nw), dtype=complex)
kpt_u = paw.wfs.kpt_u
for ij, ks_ in enumerate(lr.kss):
# TODO: better output of progress
parprint('%d/%d' % (ij, nkss))
# TODO: speedup:
# for each w, check magnitude of C_wij and
# take C_wij for those ij that contribute most
# Take copy so that memory for pair density is released
# after each loop iteration
ks = ks_.copy()
# Initialize pair density
kpt = kpt_u[ks.spin]
ks.set_paw(paw)
ks.initialize(kpt, ks.i, ks.j)
# Get pair density
# TODO: gridrefinements
yes_finegrid = gridrefinement == 2
if from_density == 'pseudo':
nij_g = ks.get(finegrid=yes_finegrid)
elif from_density == 'comp':
nij_g = ks.with_compensation_charges(finegrid=yes_finegrid)
elif from_density == 'ae':
nij_g = ks.with_ae_corrections(finegrid=yes_finegrid)
# TODO: better to split pair density in pseudo density part
# and FD_asp etc. coefficients (like in time-propagation).
# Then do gridrefinement and add AE/comp corrections afterwards
# -> speedup (no need to do summations on fine grid)
# TODO: speedup: check magnitude of C_wij (see above)
for w in range(self.nw):
Fn_wg[w] += nij_g * C_wij[w, ij]
# Return charge density (electrons = negative charge)
return - Fn_wg, gd
def solve(self, phi, rho, charge=None, eps=None, maxcharge=1e-6,
zero_initial_phi=False):
if eps is None:
eps = self.eps
actual_charge = self.gd.integrate(rho)
background = (actual_charge / self.gd.dv /
self.gd.get_size_of_global_array().prod())
if charge is None:
charge = actual_charge
if abs(charge) <= maxcharge:
# System is charge neutral. Use standard solver
return self.solve_neutral(phi, rho - background, eps=eps)
elif abs(charge) > maxcharge and self.gd.pbc_c.all():
# System is charged and periodic. Subtract a homogeneous
# background charge
if self.charged_periodic_correction is None:
parprint("""+-----------------------------------------------------+
| Calculating charged periodic correction using the |
| Ewald potential from a lattice of probe charges in |
| a homogenous background density |
+-----------------------------------------------------+""")
self.charged_periodic_correction = madelung(self.gd.cell_cv)
parprint("Potential shift will be ",
self.charged_periodic_correction , "Ha.")
# Set initial guess for potential
if zero_initial_phi:
phi[:] = 0.0
else:
phi -= charge * self.charged_periodic_correction
iters = self.solve_neutral(phi, rho - background, eps=eps)
phi += charge * self.charged_periodic_correction
return iters
elif abs(charge) > maxcharge and not self.gd.pbc_c.any():
# The system is charged and in a non-periodic unit cell.
# Determine the potential by 1) subtract a gaussian from the
# density, 2) determine potential from the neutralized density
# and 3) add the potential from the gaussian density.
# Load necessary attributes
self.load_gauss()
# Remove monopole moment
q = actual_charge / np.sqrt(4 * pi) # Monopole moment
rho_neutral = rho - q * self.rho_gauss # neutralized density
# Set initial guess for potential
if zero_initial_phi:
phi[:] = 0.0
else:
axpy(-q, self.phi_gauss, phi) #phi -= q * self.phi_gauss
# Determine potential from neutral density using standard solver
niter = self.solve_neutral(phi, rho_neutral, eps=eps)
# correct error introduced by removing monopole
axpy(q, self.phi_gauss, phi) #phi += q * self.phi_gauss
return niter
else:
# System is charged with mixed boundaryconditions
msg = 'Charged systems with mixed periodic/zero'
msg += ' boundary conditions'
raise NotImplementedError(msg)
x1 = 1 - x0
y0 = (atoms.positions[0][1] - 1.0) / atoms.get_cell()[1, 1]
y1 = 1 - y0
z0 = atoms.positions[1][2] / atoms.get_cell()[2, 2]
z1 = atoms.positions[0][2] / atoms.get_cell()[2, 2]
gd = calc.wfs.gd
Gx0, Gx1 = gd.N_c[0] * x0, gd.N_c[0] * x1
Gy0, Gy1 = gd.N_c[1] * y0, gd.N_c[1] * y1
Gz0, Gz1 = gd.N_c[2] * z0, gd.N_c[2] * z1
finegd = calc.density.finegd
gx0, gx1 = finegd.N_c[0] * x0, finegd.N_c[0] * x1
gy0, gy1 = finegd.N_c[1] * y0, finegd.N_c[1] * y1
gz0, gz1 = finegd.N_c[2] * z0, finegd.N_c[2] * z1
int1 = elf_G[Gx0:Gx1, Gy0:Gy1, Gz0:Gz1].sum() * gd.dv
int2 = elf_g[gx0:gx1, gy0:gy1, gz0:gz1].sum() * finegd.dv
parprint("Ints", int1, int2)
parprint("Min, max G", np.min(elf_G), np.max(elf_G))
parprint("Min, max g", np.min(elf_g), np.max(elf_g))
# The tested values (< r7887) do not seem to be correct
# equal(int1, 14.8078, 0.0001)
# equal(int2, 13.0331, 0.0001)
# check spin-polarized version
try:
atoms, calc = restart("COspin.gpw", txt=None, parallel={"domain": world.size})
energy_spinpol = atoms.get_potential_energy()
except:
calc.set(spinpol=True, parallel={"domain": world.size})
energy_spinpol = atoms.get_potential_energy()
calc.write("COspin.gpw", "all")
def summary(self, method='standard', direction='central',
intensity_unit_ir='(D/A)2/amu', intensity_unit_ram='au', log=stdout):
hnu = self.get_energies(method, direction)
s = 0.01 * units._e / units._c / units._hplanck
iu_ir, iu_string_ir = self.intensity_prefactor(intensity_unit_ir)
iu_ram, iu_string_ram = self.intensity_prefactor(intensity_unit_ram)
arr = []
if intensity_unit_ir == '(D/A)2/amu':
iu_format_ir = '%9.4f '
elif intensity_unit_ir == 'km/mol':
iu_string_ir = ' ' + iu_string_ir
iu_format_ir = ' %7.1f '
elif intensity_unit_ir == 'au':
iu_format_ir = '%.6e '
elif intensity_unit_ir == 'A^4 amu^-1':
iu_format_ir = '%9.4f '
if intensity_unit_ram == '(D/A)2/amu':
iu_format_ram = '%9.4f'
elif intensity_unit_ram == 'km/mol':
iu_string_ram = ' ' + iu_string_ram
iu_format_ram = ' %7.1f'
elif intensity_unit_ram == 'au':
iu_format_ram = '%.6e '
elif intensity_unit_ram == 'A^4 amu^-1':
iu_format_ram = '%9.4f '
if isinstance(log, str):
log = paropen(log, 'a')
parprint('---------------------------------------------------------------------------------------------------------------------------', file=log)
parprint(' Mode Frequency Intensity IR Intensity Raman (real) Intensity Raman (imag) Raman Ehanced', file=log)
parprint(' # meV cm^-1 ' + iu_string_ir + ' ' + iu_string_ram +
' ' + iu_string_ram + ' ' + iu_string_ram, file=log)
parprint('---------------------------------------------------------------------------------------------------------------------------', file=log)
for n, e in enumerate(hnu):
if e.imag != 0:
c = 'i'
e = e.imag
else:
c = ' '
e = e.real
arr.append([n, 1000 * e, s * e, iu_ir * self.intensities_ir[n],
iu_ram * self.intensities_ram[n].real, iu_ram *
self.intensities_ram[n].imag])
parprint(('%3d %6.1f%s %7.1f%s ' + iu_format_ir + iu_format_ram +
iu_format_ram + iu_format_ram) %
(n, 1000 * e, c, s * e, c, iu_ir * self.intensities_ir[n],
iu_ram * self.intensities_ram[n].real, iu_ram *
self.intensities_ram[n].imag, iu_ram *
self.intensities_ram_enh[n].real), file=log)
parprint(
'-----------------------------------------------------------------------------------------',
file=log)
parprint('Zero-point energy: %.3f eV' % self.get_zero_point_energy(),
file=log)
parprint('Static dipole moment: %.3f D' % self.dipole_zero, file=log)
parprint('Maximum force on atom in `equilibrium`: %.4f eV/Å' %
self.force_zero, file=log)
parprint(file=log)
np.savetxt('ram-summary.txt', np.array(arr))
# Get crack tip position
tip_x, tip_y, tip_z = a.info['fitted_crack_tip']
# Set calculator
a.set_calculator(params.calc)
# Relax positions
del a[np.logical_or(a.numbers == atomic_numbers[ACTUAL_CRACK_TIP],
a.numbers == atomic_numbers[FITTED_CRACK_TIP])]
g = a.get_array('groups')
a.set_constraint(ase.constraints.FixAtoms(mask=g==0))
a.set_calculator(params.calc)
parprint('Optimizing positions...')
opt = ase.optimize.FIRE(a, logfile=None)
opt.run(fmax=params.fmax)
parprint('...done. Converged within {0} steps.' \
.format(opt.get_number_of_steps()))
# Get atomic strain
i, j = neighbour_list("ij", a, cutoff=2.85)
deformation_gradient, residual = atomic_strain(a, ref, neighbours=(i, j))
# Get atomic stresses
virial = a.get_stresses() # Note: get_stresses returns the virial in Atomistica!
strain = full_3x3_to_Voigt_6_strain(deformation_gradient)
vol_strain, dev_strain, J3_strain = invariants(strain)
a.set_array('strain', strain)
def summary(self, method='standard', direction='central',
intensity_unit='(D/A)2/amu', log=stdout):
hnu = self.get_energies(method, direction)
s = 0.01 * units._e / units._c / units._hplanck
iu, iu_string = self.intensity_prefactor(intensity_unit)
if intensity_unit == '(D/A)2/amu':
iu_format = '%9.4f'
elif intensity_unit == 'km/mol':
iu_string = ' ' + iu_string
iu_format = ' %7.1f'
if isinstance(log, str):
log = paropen(log, 'a')
parprint('-------------------------------------', file=log)
parprint(' Mode Frequency Intensity', file=log)
parprint(' # meV cm^-1 ' + iu_string, file=log)
parprint('-------------------------------------', file=log)
for n, e in enumerate(hnu):
if e.imag != 0:
c = 'i'
e = e.imag
else:
c = ' '
parprint(('%3d %6.1f%s %7.1f%s ' + iu_format) %
(n, 1000 * e, c, s * e, c, iu * self.intensities[n]),
file=log)
parprint('-------------------------------------', file=log)
parprint('Zero-point energy: %.3f eV' % self.get_zero_point_energy(),
file=log)
parprint('Static dipole moment: %.3f D' % self.dipole_zero, file=log)
parprint('Maximum force on atom in `equilibrium`: %.4f eV/Å' %
self.force_zero, file=log)
parprint(file=log)
if 1:
c = GPAW(xc="PBE", nbands=-1, h=h)
s = Cluster([Atom("H")])
s.minimal_box(box, h=h)
c.calculate(s)
c.write(gpwname, "all")
else:
c = GPAW(gpwname)
s = c.get_atoms()
c.converge_wave_functions()
cm = s.get_center_of_mass()
Ekin = 1.0
ekin = Ekin / Ha
for form, title in [("L", "length form"), ("V", "velocity form")]:
parprint("--", title)
ds = []
for analytic in [True, False]:
if analytic:
initial = H1s(c.density.gd, cm)
else:
initial = BoundState(c, 0, 0)
initial.set_energy(-Ha / 2.0)
csb = CrossSectionBeta(initial=initial, final=None, r0=cm, ngauss=ngauss, form=form)
if analytic:
ds.append(initial.get_ds(Ekin, form))
parprint("analytic 1s energy, beta, ds %5.3f" % (Ekin + Ha / 2.0), end="")
parprint("%8.4f %12.5f" % (2, ds[-1]))
ds.append(csb.get_ds(Ekin))
parprint("numeric 1s energy, beta, ds %5.3f" % (Ekin + Ha / 2.0), end="")
def summary(self, method='standard', direction='central',
intensity_unit='(D/A)2/amu'):
hnu = self.get_energies(method, direction)
s = 0.01 * units._e / units._c / units._hplanck
if intensity_unit == '(D/A)2/amu':
iu = 1.0
iu_string = '(D/Å)^2 amu^-1'
iu_format = '%9.4f'
elif intensity_unit == 'km/mol':
# conversion factor from Porezag PRB 54 (1996) 7830
iu = 42.255
iu_string = ' km/mol'
iu_format = ' %7.1f'
else:
raise RuntimeError('Intensity unit >' + intensity_unit +
'< unknown.')
parprint('-------------------------------------')
parprint(' Mode Frequency Intensity')
parprint(' # meV cm^-1 ' + iu_string)
parprint('-------------------------------------')
for n, e in enumerate(hnu):
if e.imag != 0:
c = 'i'
e = e.imag
else:
c = ' '
parprint(('%3d %6.1f%s %7.1f%s ' + iu_format) %
(n, 1000 * e, c, s * e, c, iu * self.intensities[n]))
parprint('-------------------------------------')
parprint('Zero-point energy: %.3f eV' % self.get_zero_point_energy())
parprint('Static dipole moment: %.3f D' % self.dipole_zero)
parprint('Maximum force on atom in `equilibrium`: %.4f eV/Å' %
self.force_zero)
parprint()
# Wigner-Seitz ----------------------------------------
if 1:
ws = WignerSeitz(calc.density.finegd, mol, calc)
vr = ws.get_effective_volume_ratios()
parprint('Wigner-Seitz:', vr)
if len(lastres):
equal(vr, lastres.pop(0), 1.e-10)
results.append(vr)
return results
# calculate
parprint('fresh:')
mol = Cluster(molecule('H2O'))
mol.minimal_box(3, h=h)
calc = GPAW(nbands=6,
h = h,
txt=None)
calc.calculate(mol)
calc.write(gpwname)
lastres = run()
# load previous calculation
parprint('reloaded:')
calc = GPAW(gpwname, txt=None)
mol = calc.get_atoms()
run(lastres)
xco = HybridXC(xc)
cocc = GPAW(h=0.3, eigensolver="rmm-diis", xc=xco, nbands=nbands, convergence={"eigenstates": 1e-4}, txt=txt)
cocc.calculate(loa)
else:
cocc = GPAW(fname)
cocc.converge_wave_functions()
fo_n = 1.0 * cocc.get_occupation_numbers()
eo_n = 1.0 * cocc.get_eigenvalues()
if unocc:
# apply Fock opeartor also to unoccupied orbitals
xcu = HybridXC(xc, unocc=True)
cunocc = GPAW(h=0.3, eigensolver="rmm-diis", xc=xcu, nbands=nbands, convergence={"eigenstates": 1e-4}, txt=txt)
cunocc.calculate(loa)
parprint(" HF occ HF unocc diff")
parprint(
"Energy %10.4f %10.4f %10.4f"
% (
cocc.get_potential_energy(),
cunocc.get_potential_energy(),
cocc.get_potential_energy() - cunocc.get_potential_energy(),
)
)
equal(cocc.get_potential_energy(), cunocc.get_potential_energy(), 1.0e-4)
fu_n = cunocc.get_occupation_numbers()
eu_n = cunocc.get_eigenvalues()
parprint("Eigenvalues:")
for eo, fo, eu, fu in zip(eo_n, fo_n, eu_n, fu_n):
h = 0.3
s = Cluster(molecule('H2O'))
s.minimal_box(3., h)
gpwname = 'H2O_h' + str(h) + '.gpw'
try:
# XXX check why this fails in parallel
calc = GPAW(gpwname + 'failsinparallel', txt=None)
atoms = calc.get_atoms()
calc.density.set_positions(atoms.get_scaled_positions() % 1.0)
calc.density.interpolate_pseudo_density()
calc.density.calculate_pseudo_charge()
except IOError:
calc = GPAW(h=h, charge=0, txt=None)
calc.calculate(s)
calc.write(gpwname)
dipole_c = calc.get_dipole_moment()
parprint('Dipole', dipole_c)
center = np.array([1,1,1]) * 50.
mp = Multipole(center, calc, lmax=2)
q_L = mp.expand(-calc.density.rhot_g)
parprint('Multipole', q_L)
# The dipole moment is independent of the center
equal(dipole_c[2], q_L[2], 1e-10)
mp.to_file(calc, mode='w')
c = GPAW(gpwname)
s = c.get_atoms()
c.converge_wave_functions()
cm = s.get_center_of_mass()
Ekin = 1.
ekin = Ekin / Ha
for form in ['L', 'V']:
ds = []
for analytic in [True, False]:
if analytic:
initial = H1s(c.density.gd, cm)
else:
initial = BoundState(c, 0, 0)
initial.set_energy(-Ha / 2.)
csb = CrossSectionBeta(
initial=initial, final=None, r0=cm, ngauss=ngauss, form=form)
if analytic:
ds.append(initial.get_ds(Ekin, form))
parprint('%5.3f' % (Ekin + Ha / 2.), end='')
parprint('%7.4f %12.5f' % (2, ds[-1]))
ds.append(csb.get_ds(Ekin))
parprint('%5.3f' % (Ekin + Ha / 2.), end='')
parprint('%7.4f %12.5f' % (csb.get_beta(Ekin), ds[-1]))
parprint('error analytic GS:', int(100 * abs(ds[1] / ds[0] - 1.) + .5),
'%')
assert (abs(ds[1] / ds[0] - 1.) < 0.31)
parprint('error numeric GS:', int(100 * abs(ds[2] / ds[0] - 1.) + .5), '%')
assert (abs(ds[2] / ds[0] - 1.) < 0.2)
import matscipy.fracture_mechanics.crack as crack
###
sys.path += [ "." ]
import params
###
crack = crack.CubicCrystalCrack(params.C11, params.C12, params.C44,
params.crack_surface, params.crack_front)
# Get Griffith's k1.
k1g = crack.k1g(params.surface_energy)
parprint('Griffith k1 = %f' % k1g)
# Compute crack tip position.
if hasattr(params, 'tip_x0'):
tip_x0 = params.tip_x0
else:
tip_x0 = params.cryst.cell.diagonal()[0]/2
if hasattr(params, 'tip_y0'):
tip_y0 = params.tip_y0
else:
tip_y0 = params.cryst.cell.diagonal()[2]/2
cryst = params.cryst.copy()
a = cryst.copy()
old_k1 = params.k1[0]
ux, uy = crack.displacements(cryst.positions[:,0], cryst.positions[:,1],
# split the structures
s1 = ss.find_connected(0)
s2 = ss.find_connected(-1)
assert len(ss) == len(s1) + len(s2)
c = GPAW(xc='PBE', h=h, nbands=-6,
occupations=FermiDirac(width=0.1), txt=None)
cdf = GPAW(xc='vdW-DF', h=h, nbands=-6, occupations=FermiDirac(width=0.1),
txt=None)
for s in [s1, s2, ss]:
s.set_calculator(c)
s.minimal_box(box, h=h)
Energy['PBE'].append(s.get_potential_energy())
cc = vdWTkatchenko09prl(HirshfeldPartitioning(c),
vdWradii(s.get_chemical_symbols(), 'PBE'))
s.set_calculator(cc)
Energy['TS09'].append(s.get_potential_energy())
s.set_calculator(cdf)
Energy['vdW-DF'].append(s.get_potential_energy())
parprint('Coupled cluster binding energy',
-data[molecule]['interaction energy CC'] * 1000, 'meV')
for xc in ['PBE', 'vdW-DF', 'TS09']:
ene = Energy[xc]
# print xc, 'energies', ene
parprint(xc, 'binding energy',
(ene[0] + ene[1] - ene[2]) * 1000, 'meV')
xc='LDA'
# without spin
lr = LrTDDFT(calc, xc=xc)
lr.diagonalize()
t1 = lr[0]
lr_calc = lr
ex = ExcitedState(lr, 0)
den = ex.get_pseudo_density() * Bohr**3
# course grids
for finegrid in [1,0]:
lr = LrTDDFT(calc, xc=xc, finegrid=finegrid)
lr.diagonalize()
t3 = lr[0]
parprint('finegrid, t1, t3=', finegrid, t1 ,t3)
equal(t1.get_energy(), t3.get_energy(), 5.e-4)
# with spin
lr_vspin = LrTDDFT(calc, xc=xc, nspins=2)
singlet, triplet = lr_vspin.singlets_triplets()
lr_vspin.diagonalize()
# the triplet is lower, so that the second is the first singlet
# excited state
t2 = lr_vspin[1]
ex_vspin = ExcitedState(lr_vspin, 1)
den_vspin = ex_vspin.get_pseudo_density() * Bohr**3
parprint('with virtual/wo spin t2, t1=',
t2.get_energy(), t1 .get_energy())
name = 'zero bc'
calc = GPAW(h=0.25, nbands=4, mode=mode,
eigensolver=eigensolver, txt=txt)
Be.set_calculator(calc)
Be.get_potential_energy()
kss = KSSingles(calc)
# all s->p transitions at the same energy [Ha] and
# oscillator_strength
for ks in kss:
equal(ks.get_energy(), kss[0].get_energy(), 1.e-4)
equal(ks.get_oscillator_strength()[0],
kss[0].get_oscillator_strength()[0], 1.e-3)
energy[name] = np.array(
[ks.get_energy() * Hartree for ks in kss]).mean()
osz[name] = np.array(
[ks.get_oscillator_strength()[0] for ks in kss]).sum()
parprint(kss)
# I/O
kss.write('kss.dat')
mpi.world.barrier()
kss = KSSingles('kss.dat')
kss1 = KSSingles('kss.dat', jend=1)
assert(len(kss1) == 1)
# periodic and non-periodic should be roughly equal
equal(energy['zero bc'], energy['periodic'], 1.e-2)
equal(osz['zero bc'], osz['periodic'], 1.e-3)