Hi,
I wonder why is the band calculation much longer than a scf calcuation.
I did a calculation for a 64-atoms supercell using 20 cpu cores.
In summary, I did
1) SCF calculation with only gamma point, run in two minutes.
2) Non-self-consistent band calculation with 27 k-points.
In the nscf calculation each k-point takes 15-20 minutes and the total
calculation lasts 7 hours. I understand that for the k-points along the
line the wfc are complex, the symmetry is smaller, but even so the time
scale is quite different.
The machine has to keep all the wfc in memory, but it was not swapping.
Even the gamma point took 15 minutes, why does it takes longer than the scf
calculation?
Please, let me know if I am doing something wrong. Below are the inputs
for the scf and the bnd calculations.
SCF:
calculation = 'scf'
restart_mode='from_scratch',
pseudo_dir = "./",
outdir="./tmp/",
tstress = .true.,
tprnfor = .true. ,
prefix= 'cdte64',
disk_io = 'low',
etot_conv_thr = 1.0D-3,
wf_collect=.TRUE.,
verbosity='high'
/
ibrav= 1,
celldm(1) = 25.02,
nat = 64,
ntyp = 2,
ecutwfc = 28.67,
ecutrho = 180,
degauss = 0.001D0,
occupations = "smearing",
smearing = "gauss",
tot_charge = 0,
nspin = 1 , ! set to 2 for spin polarized
! tot_magnetization = 0 , ! change to 1
/
diagonalization='david'
conv_thr = 1.D-6,
mixing_beta = 0.4D0,
diago_david_ndim= 2,
/
pot_extrapolation='second_order',
trust_radius_max = 0.7,
trust_radius_ini = 0.7,
/
ATOMIC_SPECIES
Cd 112.411 cd_pbe_v1.uspp.F.UPF
Te 127.600 te_pbe_v1.uspp.F.UPF
ATOMIC_POSITIONS (alat)
Cd 0.5000 0.5000 0.5000
Cd 0. 0. 0.
Cd 0.2500 0.2500 0.
….
K_POINTS gamma
The NSCF band calculation input is:
calculation = 'bands'
! restart_mode='from_scratch',
pseudo_dir = "./",
outdir="./tmp/",
tstress = .true.,
tprnfor = .true. ,
prefix= 'cdte64',
disk_io = 'low',
etot_conv_thr = 1.0D-3,
verbosity='high'
/
ibrav= 1,
celldm(1) = 25.02,
nat = 64,
ntyp = 2,
ecutwfc = 28.67,
ecutrho = 180,
degauss = 0.001D0,
occupations = "smearing",
smearing = "gauss",
tot_charge = 0,
nspin = 1 , ! set to 2 for spin polarized
! tot_magnetization = 0 , ! change to 1
/
diagonalization='david'
conv_thr = 1.D-6,
mixing_beta = 0.4D0,
diago_david_ndim= 2,
/
pot_extrapolation='second_order',
trust_radius_max = 0.7,
trust_radius_ini = 0.7,
/
ATOMIC_SPECIES
Cd 112.411 cd_pbe_v1.uspp.F.UPF
Te 127.600 te_pbe_v1.uspp.F.UPF
ATOMIC_POSITIONS (alat)
Cd 0.5000 0.5000 0.5000
Cd 0. 0. 0.
Cd 0.2500 0.2500 0.
….
K_POINTS crystal_b
3
0.500 0.500 0.500 17
0.000 0.000 0.000 10
0.500 0.000 0.000 1
Thank you.
Eduardo Menendez Proupin
Departamento de Fisica, Facultad de Ciencias, Universidad de Chile
URL: http://www.gnm.cl/emenendez
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