Dear Pascal,

You can try the older pseudo and see whether it works - in the case of tungsten I created my own pseudo which is just slightly different from the one of the PS library. Yet, I don't know anymore what I changed and I'm already on Christmas vacation. It had to do with using a certain type of function (bessel or something like this?)... I could help you with that in January ;)

Regards

Thomas

Zitat von pboulet <[email protected]>:

Dear Marko and Thomas,

I ran the tests you suggested, the problem comes from the Rh relativistic pseudopotential. The others are okay, even with the occupations fixed (there is a large gap anyway).

I may try the older psp of Rh available in the pslibrary, or do you have other suggestion(s)?

Thank you
Best regards
Pascal



Pascal Boulet
—
Professor in computational materials - DEPARTMENT OF CHEMISTRY
Aix-Marseille University - Avenue Escadrille Normandie Niemen - F-13013 Marseille - FRANCE
Tél: +33(0)4 13 55 18 10 - Fax : +33(0)4 13 55 18 50
Email : [email protected] <mailto:[email protected]>







Le 19 déc. 2019 à 20:53, Mladenovic Marko <[email protected]> a écrit :

I would also try non-fixed occupancies and different pseudopotentials (in line to what Thomas proposed).

Marko
________________________________
From: users <[email protected] <mailto:[email protected]>> on behalf of Dr. Thomas Brumme <[email protected] <mailto:[email protected]>>
Sent: Thursday, December 19, 2019 7:03:25 PM
To: [email protected] <mailto:[email protected]>; [email protected] <mailto:[email protected]>
Subject: Re: [QE-users] Problem with SCF including spin-orbit coupling

Dear Pascal,

If the non-SOC calculation converged, try to replace sthe pseudos one
by one with the relativistic ones - I know for example that the
relativistic tungsten potential of the PS library had (has?) some
problems. You could have the same problem. If it is a specific pseudo
we can try to change/improve it ;)

Thomas

Zitat von pboulet <[email protected] <mailto:[email protected]>>:

Hello Marko,

Thank you for your prompt response.

I copy-pasted the wrong input file. The right one is a SCF one (the
nscf should be subsequent to scf):
&CONTROL
 calculation   ='scf',
 nstep         = 200,
 etot_conv_thr = 1.d-7,
!  forc_conv_thr = 1.d-4,
 wfcdir        = './WFC' ,
!  tstress       = .true.,
 prefix        = 'STe_scf_LS',
 pseudo_dir    = '/scratch/cnt0022/pmc6881/paboulet/pseudo/',
 verbosity     = 'high',
 restart_mode  = ‘from_scratch',
 wf_collect    = .true.,
 disk_io       = 'high',

The rest is the same as in my previous email, except for the
k-points: 12x12x4 1 1 1, as in the non-SO optimisation.

Pascal


Le 19 déc. 2019 à 17:42, Mladenovic Marko
<[email protected] <mailto:[email protected]>> a écrit :

Hello Pascal,

it seems that you are performing a non-scf calculation (calculation
 ='nscf') and you are restarting an other calculation
(restart_mode  = 'restart'). Is this what you want?

Best,
Marko
From: users <[email protected] <mailto:[email protected]>> on behalf of
pboulet <[email protected] <mailto:[email protected]>>
Sent: Thursday, December 19, 2019 5:03:40 PM
To: Quantum Espresso users Forum
Subject: [QE-users] Problem with SCF including spin-orbit coupling

Dear All,

I have some troubles with a SCF calculation using SOC (QE 6.1).
I have optimised a structure with non-SOC pseudopotentials and now
I want to perform a SCF calculation by including SOC to get the
electronic band structure. The problem is that the SCF diverges
right away as you can see here:

Self-consistent Calculation

    iteration #  1     ecut=    35.00 Ry     beta=0.10
    Davidson diagonalization with overlap
    ethr =  1.00E-05,  avg # of iterations = 14.2

    negative rho (up, down):  8.197E+02 0.000E+00

    total cpu time spent up to now is     2293.7 secs

    total energy              =  -16093.90449193 Ry
    Harris-Foulkes estimate   =  -18277.15379034 Ry
    estimated scf accuracy    < 5077678.52441197 Ry

    iteration #  2     ecut=    35.00 Ry     beta=0.10
    Davidson diagonalization with overlap
    ethr =  1.00E-02,  avg # of iterations =  5.0

    negative rho (up, down):  2.677E+03 0.000E+00

    total cpu time spent up to now is     3119.6 secs

    total energy              =   79024.56634461 Ry
    Harris-Foulkes estimate   =  -17101.52000727 Ry
    estimated scf accuracy    < 4036754.22296032 Ry

    iteration #  3     ecut=    35.00 Ry     beta=0.10
    Davidson diagonalization with overlap
    ethr =  1.00E-02,  avg # of iterations =  6.0

    negative rho (up, down):  2.815E+03 0.000E+00

    total cpu time spent up to now is     4658.4 secs

    total energy              =  132135.46722241 Ry
    Harris-Foulkes estimate   = -142275.32127673 Ry
    estimated scf accuracy    < 6116470.38137350 Ry
<<<<<

I am using PAW pseudopotentials (Ba, Rh, Ge and S) from the PSL
library.  The cg diagonalisation does not solve the problem.

Here is a piece of the input file:
&CONTROL
 calculation   ='nscf',
 nstep         = 300,
 etot_conv_thr = 1.d-7,
 forc_conv_thr = 1.d-4,
 wfcdir        = './WFC' ,
 prefix        = 'STe_nscf_LS',
 pseudo_dir    = '/scratch/cnt0022/pmc6881/paboulet/pseudo/',
 verbosity     = 'high',
 restart_mode  = 'restart',
 wf_collect    = .true.,
 disk_io       = 'high',
/
&SYSTEM
!  celldm(1)   = 1.0,
 nat         = 52,
 ntyp        = 5,
 ibrav       = 0,
 ecutwfc     = 35.d0,
 ecutrho     = 350.d0,
 occupations = 'fixed',
 nbnd        = 630,
 lspinorb    = .true.,
 noncolin    = .true.,
 nr1 = 72, nr2 = 72, nr3 = 360,
/
&ELECTRONS
 electron_maxstep = 200,
 conv_thr         = 1.d-10,
 mixing_beta      = 0.2d0,
 diagonalization  = 'david',
/

K_POINTS automatic
16 16 8 0 0 0

ATOMIC_SPECIES
Ba 137.3270   Ba.rel-pbe-spn-kjpaw_psl.1.0.0.UPF,
Rh 102.9055   Rh.rel-pbe-spn-kjpaw_psl.1.0.0.UPF,
Ge  72.6400   Ge.rel-pbe-dn-kjpaw_psl.1.0.0.UPF,
S   32.0650   S.rel-pbe-nl-kjpaw_psl.1.0.0.UPF,
Te 127.6000   Te.rel-pbe-dn-kjpaw_psl.0.2.2.UPF

etc…


Do you have a special recipe for this type of calculation?

Thank you,
Best regards

Pascal Boulet
—
Professor in computational materials - DEPARTMENT OF CHEMISTRY
Aix-Marseille University - Avenue Escadrille Normandie Niemen -
F-13013 Marseille - FRANCE
Tél: +33(0)4 13 55 18 10 - Fax : +33(0)4 13 55 18 50
Email : [email protected] <mailto:[email protected]> <mailto:[email protected] <mailto:[email protected]>>







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--
Dr. rer. nat. Thomas Brumme
Wilhelm-Ostwald-Institute for Physical and Theoretical Chemistry
Leipzig University
Phillipp-Rosenthal-Strasse 31
04103 Leipzig
Tel: +49 (0)341 97 36456
email: [email protected]

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