sfBSE/output/H2/SF-TDDFT/bhhlyp/h2_0.65.log
2021-01-22 16:55:53 +01:00

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Running Job 1 of 1 h2_0.65.inp
qchem h2_0.65.inp_28915.0 /mnt/beegfs/tmpdir/qchem28915/ 0
/share/apps/common/q-chem/5.2.1/exe/qcprog.exe_s h2_0.65.inp_28915.0 /mnt/beegfs/tmpdir/qchem28915/
Welcome to Q-Chem
A Quantum Leap Into The Future Of Chemistry
Q-Chem 5.2, Q-Chem, Inc., Pleasanton, CA (2019)
Yihan Shao, Zhengting Gan, E. Epifanovsky, A. T. B. Gilbert, M. Wormit,
J. Kussmann, A. W. Lange, A. Behn, Jia Deng, Xintian Feng, D. Ghosh,
M. Goldey, P. R. Horn, L. D. Jacobson, I. Kaliman, T. Kus, A. Landau,
Jie Liu, E. I. Proynov, R. M. Richard, R. P. Steele, E. J. Sundstrom,
H. L. Woodcock III, P. M. Zimmerman, D. Zuev, B. Albrecht, E. Alguire,
S. A. Baeppler, D. Barton, Z. Benda, Y. A. Bernard, E. J. Berquist,
K. B. Bravaya, H. Burton, D. Casanova, Chun-Min Chang, Yunqing Chen,
A. Chien, K. D. Closser, M. P. Coons, S. Coriani, S. Dasgupta,
A. L. Dempwolff, M. Diedenhofen, Hainam Do, R. G. Edgar, Po-Tung Fang,
S. Faraji, S. Fatehi, Qingguo Feng, K. D. Fenk, J. Fosso-Tande,
J. Gayvert, Qinghui Ge, A. Ghysels, G. Gidofalvi, J. Gomes,
J. Gonthier, A. Gunina, D. Hait, M. W. D. Hanson-Heine,
P. H. P. Harbach, A. W. Hauser, M. F. Herbst, J. E. Herr,
E. G. Hohenstein, Z. C. Holden, Kerwin Hui, B. C. Huynh, T.-C. Jagau,
Hyunjun Ji, B. Kaduk, K. Khistyaev, Jaehoon Kim, P. Klunzinger, K. Koh,
D. Kosenkov, L. Koulias, T. Kowalczyk, C. M. Krauter, A. Kunitsa,
Ka Un Lao, A. Laurent, K. V. Lawler, Joonho Lee, D. Lefrancois,
S. Lehtola, D. S. Levine, Yi-Pei Li, You-Sheng Lin, Fenglai Liu,
E. Livshits, A. Luenser, P. Manohar, E. Mansoor, S. F. Manzer,
Shan-Ping Mao, Yuezhi Mao, N. Mardirossian, A. V. Marenich,
T. Markovich, L. A. Martinez-Martinez, S. A. Maurer, N. J. Mayhall,
S. C. McKenzie, J.-M. Mewes, P. Morgante, A. F. Morrison,
J. W. Mullinax, K. Nanda, T. S. Nguyen-Beck, R. Olivares-Amaya,
J. A. Parkhill, Zheng Pei, T. M. Perrine, F. Plasser, P. Pokhilko,
S. Prager, A. Prociuk, E. Ramos, D. R. Rehn, F. Rob, M. Scheurer,
M. Schneider, N. Sergueev, S. M. Sharada, S. Sharma, D. W. Small,
T. Stauch, T. Stein, Yu-Chuan Su, A. J. W. Thom, A. Tkatchenko,
T. Tsuchimochi, N. M. Tubman, L. Vogt, M. L. Vidal, O. Vydrov,
M. A. Watson, J. Wenzel, M. de Wergifosse, T. A. Wesolowski, A. White,
J. Witte, A. Yamada, Jun Yang, K. Yao, S. Yeganeh, S. R. Yost,
Zhi-Qiang You, A. Zech, Igor Ying Zhang, Xing Zhang, Yan Zhao,
Ying Zhu, B. R. Brooks, G. K. L. Chan, C. J. Cramer, M. S. Gordon,
W. J. Hehre, A. Klamt, M. W. Schmidt, C. D. Sherrill, D. G. Truhlar,
A. Aspuru-Guzik, R. Baer, A. T. Bell, N. A. Besley, Jeng-Da Chai,
A. E. DePrince, III, R. A. DiStasio Jr., A. Dreuw, B. D. Dunietz,
T. R. Furlani, Chao-Ping Hsu, Yousung Jung, Jing Kong, D. S. Lambrecht,
WanZhen Liang, C. Ochsenfeld, V. A. Rassolov, L. V. Slipchenko,
J. E. Subotnik, T. Van Voorhis, J. M. Herbert, A. I. Krylov,
P. M. W. Gill, M. Head-Gordon
Contributors to earlier versions of Q-Chem not listed above:
R. D. Adamson, B. Austin, J. Baker, G. J. O. Beran, K. Brandhorst,
S. T. Brown, E. F. C. Byrd, A. K. Chakraborty, C.-L. Cheng,
Siu Hung Chien, D. M. Chipman, D. L. Crittenden, H. Dachsel,
R. J. Doerksen, A. D. Dutoi, L. Fusti-Molnar, W. A. Goddard III,
A. Golubeva-Zadorozhnaya, S. R. Gwaltney, G. Hawkins, A. Heyden,
S. Hirata, G. Kedziora, F. J. Keil, C. Kelley, Jihan Kim, R. A. King,
R. Z. Khaliullin, P. P. Korambath, W. Kurlancheek, A. M. Lee, M. S. Lee,
S. V. Levchenko, Ching Yeh Lin, D. Liotard, R. C. Lochan, I. Lotan,
P. E. Maslen, N. Nair, D. P. O'Neill, D. Neuhauser, E. Neuscamman,
C. M. Oana, R. Olson, B. Peters, R. Peverati, P. A. Pieniazek,
Y. M. Rhee, J. Ritchie, M. A. Rohrdanz, E. Rosta, N. J. Russ,
H. F. Schaefer III, N. E. Schultz, N. Shenvi, A. C. Simmonett, A. Sodt,
D. Stuck, K. S. Thanthiriwatte, V. Vanovschi, Tao Wang, A. Warshel,
C. F. Williams, Q. Wu, X. Xu, W. Zhang
Please cite Q-Chem as follows:
Y. Shao et al., Mol. Phys. 113, 184-215 (2015)
DOI: 10.1080/00268976.2014.952696
Q-Chem 5.2.1 for Intel X86 EM64T Linux
Parts of Q-Chem use Armadillo 8.300.2 (Tropical Shenanigans).
http://arma.sourceforge.net/
Q-Chem begins on Fri Jan 22 16:31:45 2021
Host:
0
Scratch files written to /mnt/beegfs/tmpdir/qchem28915//
Jul1719 |scratch|qcdevops|jenkins|workspace|build_RNUM 6358
Processing $rem in /share/apps/common/q-chem/5.2.1/config/preferences:
MEM_TOTAL 5000
NAlpha2: 4
NElect 2
Mult 3
Checking the input file for inconsistencies... ...done.
--------------------------------------------------------------
User input:
--------------------------------------------------------------
$comment
SF-TDDFT
$end
$molecule
0 3
H 0 0 0
H 0 0 0.65
$end
$rem
JOBTYPE = sp
METHOD = BHHLYP
BASIS = CC-PVQZ
PURECART = 2222
SCF_CONVERGENCE = 9
THRESH = 12
MAX_SCF_CYCLES = 100
MAX_CIS_CYCLES = 100
SPIN_FLIP = TRUE
UNRESTRICTED = TRUE
CIS_N_ROOTS = 20
RPA = FALSE
$end
--------------------------------------------------------------
----------------------------------------------------------------
Standard Nuclear Orientation (Angstroms)
I Atom X Y Z
----------------------------------------------------------------
1 H 0.0000000000 0.0000000000 -0.3250000000
2 H 0.0000000000 0.0000000000 0.3250000000
----------------------------------------------------------------
Molecular Point Group D*h NOp =***
Largest Abelian Subgroup D2h NOp = 1
Nuclear Repulsion Energy = 0.81411879 hartrees
There are 2 alpha and 0 beta electrons
Q-Chem warning in module forms1/BasisType.C, line 1983:
You are not using the predefined 5D/6D in this basis set.
Requested basis set is cc-pVQZ
There are 20 shells and 70 basis functions
Total QAlloc Memory Limit 5000 MB
Mega-Array Size 188 MB
MEM_STATIC part 192 MB
Distance Matrix (Angstroms)
H ( 1)
H ( 2) 0.650000
A cutoff of 1.0D-12 yielded 210 shell pairs
There are 2653 function pairs
Smallest overlap matrix eigenvalue = 1.59E-05
Scale SEOQF with 1.000000e+00/1.000000e+00/1.000000e+00
Standard Electronic Orientation quadrupole field applied
Nucleus-field energy = -0.0000000002 hartrees
Guess from superposition of atomic densities
Warning: Energy on first SCF cycle will be non-variational
SAD guess density has 0.090382 electrons
-----------------------------------------------------------------------
General SCF calculation program by
Eric Jon Sundstrom, Paul Horn, Yuezhi Mao, Dmitri Zuev, Alec White,
David Stuck, Shaama M.S., Shane Yost, Joonho Lee, David Small,
Daniel Levine, Susi Lehtola, Hugh Burton, Evgeny Epifanovsky,
Bang C. Huynh
-----------------------------------------------------------------------
Exchange: 0.5000 Hartree-Fock + 0.5000 B88
Correlation: 1.0000 LYP
Using SG-1 standard quadrature grid
A unrestricted SCF calculation will be
performed using DIIS
SCF converges when DIIS error is below 1.0e-09
---------------------------------------
Cycle Energy DIIS error
---------------------------------------
1 0.6898878964 1.13e-03
2 19.0841043957 1.70e-01
3 19.0807572741 1.70e-01
4 19.0792730940 1.70e-01
5 19.0817908241 1.70e-01
6 19.0813336675 1.70e-01
7 19.0816631788 1.70e-01
8 19.0816081932 1.70e-01
9 19.0816914051 1.70e-01
10 19.0814191868 1.70e-01
11 19.0814220129 1.70e-01
12 19.0813829221 1.70e-01
13 19.0806803778 1.70e-01
14 19.0823016128 1.70e-01
15 19.0824064203 1.70e-01
16 19.0823340371 1.70e-01
17 -0.6700386824 3.68e-03
18 -0.7229344219 2.61e-04
19 -0.7233833345 6.75e-05
20 -0.7234433544 1.80e-05
21 -0.7234538512 4.66e-06
22 -0.7234546661 8.34e-07
23 -0.7234546800 2.66e-08
24 -0.7234546800 2.48e-09
25 -0.7234546800 2.87e-10 Convergence criterion met
---------------------------------------
SCF time: CPU 3.70s wall 4.00s
<S^2> = 2.000000000
SCF energy in the final basis set = -0.7234546800
Total energy in the final basis set = -0.7234546800
Spin-flip DFT calculation will be performed
CIS energy converged when residual is below 10e- 6
---------------------------------------------------
Iter Rts Conv Rts Left Ttl Dev Max Dev
---------------------------------------------------
1 0 20 0.056691 0.005558
2 0 20 0.002409 0.000669
3 9 11 0.000044 0.000012
4 20 0 0.000004 0.000001 Roots Converged
---------------------------------------------------
---------------------------------------------------
SF-DFT Excitation Energies
(The first "excited" state might be the ground state)
---------------------------------------------------
Excited state 1: excitation energy (eV) = -6.9334
Total energy for state 1: -0.97825383 au
<S**2> : 0.0391
S( 2) --> S( 1) amplitude = 0.9971 alpha
Excited state 2: excitation energy (eV) = 3.8344
Total energy for state 2: -0.58254250 au
<S**2> : 1.2894
S( 1) --> S( 1) amplitude = 0.1536 alpha
S( 2) --> S( 2) amplitude = 0.9796 alpha
Excited state 3: excitation energy (eV) = 5.3754
Total energy for state 3: -0.52591311 au
<S**2> : 0.9727
S( 2) --> V( 1) amplitude = 0.9966 alpha
Excited state 4: excitation energy (eV) = 7.7668
Total energy for state 4: -0.43803078 au
<S**2> : 0.8122
S( 1) --> S( 1) amplitude = 0.9562 alpha
S( 1) --> V( 1) amplitude = 0.1624 alpha
S( 2) --> S( 2) amplitude = -0.1723 alpha
S( 2) --> V( 4) amplitude = 0.1534 alpha
Excited state 5: excitation energy (eV) = 10.2278
Total energy for state 5: -0.34758882 au
<S**2> : 1.0000
S( 2) --> V( 3) amplitude = 0.9995 alpha
Excited state 6: excitation energy (eV) = 10.2278
Total energy for state 6: -0.34758882 au
<S**2> : 1.0000
S( 2) --> V( 2) amplitude = 0.9995 alpha
Excited state 7: excitation energy (eV) = 13.0336
Total energy for state 7: -0.24447866 au
<S**2> : 0.9023
S( 1) --> S( 1) amplitude = -0.1735 alpha
S( 2) --> V( 4) amplitude = 0.9786 alpha
Excited state 8: excitation energy (eV) = 19.1302
Total energy for state 8: -0.02043404 au
<S**2> : 0.9679
S( 1) --> S( 2) amplitude = -0.1642 alpha
S( 2) --> V( 7) amplitude = 0.9831 alpha
Excited state 9: excitation energy (eV) = 19.1838
Total energy for state 9: -0.01846262 au
<S**2> : 1.0000
S( 2) --> V( 6) amplitude = 0.9971 alpha
Excited state 10: excitation energy (eV) = 19.1838
Total energy for state 10: -0.01846262 au
<S**2> : 1.0000
S( 2) --> V( 5) amplitude = 0.9971 alpha
Excited state 11: excitation energy (eV) = 22.4960
Total energy for state 11: 0.10325849 au
<S**2> : 0.0669
S( 1) --> S( 2) amplitude = 0.9606 alpha
S( 1) --> V( 4) amplitude = 0.2075 alpha
S( 2) --> V( 7) amplitude = 0.1752 alpha
Excited state 12: excitation energy (eV) = 23.4953
Total energy for state 12: 0.13998214 au
<S**2> : 1.0013
S( 1) --> S( 1) amplitude = -0.1686 alpha
S( 1) --> V( 1) amplitude = 0.9800 alpha
Excited state 13: excitation energy (eV) = 25.4382
Total energy for state 13: 0.21138381 au
<S**2> : 0.9891
S( 2) --> V( 8) amplitude = 0.9979 alpha
Excited state 14: excitation energy (eV) = 27.5344
Total energy for state 14: 0.28841593 au
<S**2> : 1.0000
S( 1) --> V( 3) amplitude = 0.9954 alpha
Excited state 15: excitation energy (eV) = 27.5344
Total energy for state 15: 0.28841593 au
<S**2> : 1.0000
S( 1) --> V( 2) amplitude = 0.9954 alpha
Excited state 16: excitation energy (eV) = 27.7306
Total energy for state 16: 0.29562634 au
<S**2> : 1.0000
S( 2) --> V( 9) amplitude = 0.9982 alpha
Excited state 17: excitation energy (eV) = 30.5060
Total energy for state 17: 0.39762153 au
<S**2> : 0.9677
S( 1) --> S( 2) amplitude = -0.2189 alpha
S( 1) --> V( 4) amplitude = 0.9685 alpha
Excited state 18: excitation energy (eV) = 35.1812
Total energy for state 18: 0.56942968 au
<S**2> : 0.9961
S( 2) --> V( 10) amplitude = 0.9883 alpha
Excited state 19: excitation energy (eV) = 37.4337
Total energy for state 19: 0.65221003 au
<S**2> : 1.0000
S( 1) --> V( 6) amplitude = 0.9988 alpha
Excited state 20: excitation energy (eV) = 37.4337
Total energy for state 20: 0.65221003 au
<S**2> : 1.0000
S( 1) --> V( 5) amplitude = 0.9988 alpha
---------------------------------------------------
SETman timing summary (seconds)
CPU time 1.06s
System time 0.00s
Wall time 1.29s
--------------------------------------------------------------
Orbital Energies (a.u.)
--------------------------------------------------------------
Alpha MOs
-- Occupied --
-0.8213 -0.1241
-- Virtual --
0.0888 0.2767 0.2767 0.2984 0.5836 0.6086 0.6086 0.8197
0.9407 1.1187 1.4129 1.4129 1.6664 1.6665 1.8255 1.9584
1.9584 2.3136 2.3136 2.3148 2.3148 2.4447 2.5558 2.9336
3.1433 3.1433 3.2045 3.8506 3.8506 4.2712 4.7639 4.7639
4.8789 5.2992 5.2992 6.0382 6.0382 6.5055 6.5055 6.9473
6.9473 6.9495 7.0242 7.0243 7.1940 7.3826 7.3826 7.4809
7.4810 8.1087 8.1087 8.3041 8.9886 9.3769 9.3772 9.4073
9.4073 9.4502 9.4741 9.4741 9.7687 12.6431 13.0791 13.2376
13.2376 16.6997 26.2554 27.7362
--------------------------------------------------------------
Ground-State Mulliken Net Atomic Charges
Atom Charge (a.u.) Spin (a.u.)
--------------------------------------------------------
1 H -0.000000 1.000000
2 H 0.000000 1.000000
--------------------------------------------------------
Sum of atomic charges = 0.000000
Sum of spin charges = 2.000000
-----------------------------------------------------------------
Cartesian Multipole Moments
-----------------------------------------------------------------
Charge (ESU x 10^10)
0.0000
Dipole Moment (Debye)
X -0.0000 Y -0.0000 Z -0.0000
Tot 0.0000
Quadrupole Moments (Debye-Ang)
XX -3.1980 XY -0.0000 YY -3.1980
XZ 0.0000 YZ 0.0000 ZZ -7.8943
Octopole Moments (Debye-Ang^2)
XXX -0.0000 XXY -0.0000 XYY -0.0000
YYY -0.0000 XXZ -0.0000 XYZ -0.0000
YYZ -0.0000 XZZ -0.0000 YZZ -0.0000
ZZZ -0.0000
Hexadecapole Moments (Debye-Ang^3)
XXXX -5.4739 XXXY -0.0000 XXYY -1.8246
XYYY -0.0000 YYYY -5.4739 XXXZ 0.0000
XXYZ 0.0000 XYYZ 0.0000 YYYZ 0.0000
XXZZ -5.3889 XYZZ -0.0000 YYZZ -5.3889
XZZZ 0.0000 YZZZ 0.0000 ZZZZ -27.5841
-----------------------------------------------------------------
Archival summary:
1\1\lcpq-curie.ups-tlse.fr\SP\ProcedureUnspecified\BasisUnspecified\2(3)\emonino\FriJan2216:31:502021FriJan2216:31:502021\0\\#,ProcedureUnspecified,BasisUnspecified,\\0,3\H\H,1,0.65\\\@
Total job time: 5.35s(wall), 4.88s(cpu)
Fri Jan 22 16:31:50 2021
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