[CP2K-user] [CP2K:12536] Unable to converge for perovskite calculation

Krack Matthias (PSI) matthi... at psi.ch
Mon Nov 25 08:18:24 UTC 2019


Hi Jiapeng

I am afraid that is not possible.

Matthias

From: cp... at googlegroups.com <cp... at googlegroups.com> On Behalf Of Jiapeng Liu
Sent: Montag, 25. November 2019 05:44
To: cp2k <cp... at googlegroups.com>
Subject: Re: [CP2K:12536] Unable to converge for perovskite calculation

Dear Matthias,

Thank you very much. I used a larger cell and it converged successfully. May I ask you another question that is it possible to use CP2K to conduct a small cell calculation with no KPOINTS as in my previous case. Since I run the test in my desktop, too many atoms are not manageable. Thank you.

Regards,
Jiapeng

On Monday, November 25, 2019 at 1:00:08 AM UTC+8, Matthias Krack wrote:
Hi

That result is not a surprise, since you did not follow my first and most important suggestion which was to employ multiple unit cells.

Matthias

Von: c... at googlegroups.com<javascript:> <c... at googlegroups.com<javascript:>> Im Auftrag von Jiapeng Liu
Gesendet: Sonntag, 24. November 2019 15:42
An: cp2k <c... at googlegroups.com<javascript:>>
Betreff: Re: [CP2K:12534] Unable to converge for perovskite calculation

Dear Matthias,

Thank you for your reply. I tried with higher smearing temperature (600K) together with the default GPW method, the scf calculation accelerates with a short time. However, the scf still does not converge and the energy does not decrease monotonically. The energy just oscillates. I am not sure if this is normal? Also, does higher smearing temperature (600K) affect the final energy? Thank you.

On Friday, November 22, 2019 at 4:47:13 PM UTC+8, Matthias Krack wrote:
Hi

Without k points you will need a larger simulation cell, i.e. multiple unit cells, e.g. 4x4x2. A larger electronic temperature for the smearing might also help initially. With a larger cutoff, it might also be possible to use the default GPW method instead of GAPW in the beginning.

Matthias

From: c... at googlegroups.com<mailto:c... at googlegroups.com> <c... at googlegroups.com<mailto:c... at googlegroups.com>> On Behalf Of Jiapeng Liu
Sent: Freitag, 22. November 2019 01:47
To: cp2k <c... at googlegroups.com<mailto:c... at googlegroups.com>>
Subject: [CP2K:12529] Unable to converge for perovskite calculation

Dear CP2K users,

I repost the problem with the expectation that anyone can help me to solve this. I would like to perform the DFT+U calculations for a small perovskite cubic cell, which contains 10 atoms in total. As a first step suggested by this group, I conduct the DFT without U firstly. However, the scf fails to converge even after 3 outer scf each with 200 steps. I am quite confused about this. Can anyone help me with this, your suggestions or advice are significantly appreciated. Thank you. Following is the input file

!*************************GLOBAL SETTINGS**********************************
&GLOBAL
  PRINT_LEVEL LOW
  PROJECT_NAME LCTN_exsolution
  RUN_TYPE CELL_OPT
  SAVE_MEM T
&END GLOBAL

!*************************MOTION SETTINGS**********************************
&MOTION
  &CELL_OPT
    OPTIMIZER LBFGS
    TYPE DIRECT_CELL_OPT
  &END CELL_OPT
&END MOTION

!************************FORCE_EVAL SETTINGS********************************
&FORCE_EVAL
  STRESS_TENSOR ANALYTICAL
  METHOD QS
!********************FORCE_EVAL -> DFT SETTINGS*****************************
  &DFT
    BASIS_SET_FILE_NAME BASIS_MOLOPT_UCL
    BASIS_SET_FILE_NAME BASIS_MOLOPT
    POTENTIAL_FILE_NAME GTH_POTENTIALS
    UKS T
    CHARGE 0
    MULTIPLICITY 2
!    PLUS_U_METHOD LOWDIN
!****************FORCE_EVAL -> DFT -> SCF SETTINGS**************************
    &SCF
      ADDED_MOS 100
      MAX_SCF 200
      EPS_SCF 1.0E-6
      SCF_GUESS RESTART
      &DIAGONALIZATION T
        ALGORITHM STANDARD
      &END DIAGONALIZATION
      &OUTER_SCF
        EPS_SCF 1.0E-5
        MAX_SCF 5
      &END OUTER_SCF
      &SMEAR T
        METHOD FERMI_DIRAC
        ELECTRONIC_TEMPERATURE [K] 300
      &END SMEAR
      &MIXING T
        METHOD BROYDEN_MIXING
        ALPHA 0.4
        BETA [bohr^-1] 2
        NMIXING 5
        NBUFFER 8
      &END MIXING
    &END SCF
!****************FORCE_EVAL -> DFT -> QS SETTINGS***************************
    &QS
      EPS_DEFAULT 1.0E-12
      EXTRAPOLATION USE_GUESS
      METHOD GAPW
    &END QS
!***************FORCE_EVAL -> DFT -> GRID SETTINGS**************************
    &MGRID
      NGRIDS 5
      CUTOFF [Ry] 600
      REL_CUTOFF [Ry] 60
    &END MGRID
!*****************FORCE_EVAL -> DFT -> XC SETTINGS**************************
    &XC
      FUNCTIONAL_ROUTINE NEW
      &XC_FUNCTIONAL PBE
      &END XC_FUNCTIONAL
    &END XC
!***************FORCE_EVAL -> DFT -> POISSON SETTINGS************************
    &POISSON
      POISSON_SOLVER PERIODIC
      PERIODIC XYZ
    &END POISSON
  &END DFT
!********************FORCE_EVAL -> SUBSYS SETTINGS***************************
  &SUBSYS
    &CELL
      ABC [angstrom] 3.857 3.857 7.714
      ALPHA_BETA_GAMMA [deg] 90 90 90
      PERIODIC XYZ
      MULTIPLE_UNIT_CELL 1 1 1
    &END CELL
    &KIND La
      ELEMENT La
      BASIS_SET DZVP-MOLOPT-SR-GTH
      POTENTIAL GTH-PBE-q11
    &END KIND
    &KIND Ca
      ELEMENT Ca
      BASIS_SET DZVP-MOLOPT-SR-GTH
      POTENTIAL GTH-PBE-q10
    &END KIND
    &KIND Ti
      ELEMENT Ti
      BASIS_SET DZVP-MOLOPT-SR-GTH
      POTENTIAL GTH-PBE-q12
!      MAGNETIZATION 3.0
    &END KIND
    &KIND Ni
      ELEMENT Ni
      BASIS_SET DZVP-MOLOPT-SR-GTH
      POTENTIAL GTH-PBE-q18
!      MAGNETIZATION 3.0
!      &DFT_PLUS_U T
!        L 2
!        U_MINUS_J [eV] 6.4
!      &END DFT_PLUS_U
    &END KIND
    &KIND O
      ELEMENT O
      BASIS_SET DZVP-MOLOPT-SR-GTH
      POTENTIAL GTH-PBE-q6
    &END KIND
    &TOPOLOGY
      COORD_FILE_NAME lctn_112.xyz<http://lctn_112.xyz>
      COORD_FILE_FORMAT XYZ
      MULTIPLE_UNIT_CELL 1 1 1
    &END TOPOLOGY
  &END SUBSYS

!********************FORCE_EVAL -> PRINT SETTINGS****************************
  &PRINT
    &FORCES ON
    &END FORCES
  &END PRINT
&END FORCE_EVAL

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