sfBSE/output/H2/SF-TDDFT/bhhlyp/h2_2.75.log
2021-01-22 16:55:53 +01:00

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Running Job 1 of 1 h2_2.75.inp
qchem h2_2.75.inp_11608.0 /mnt/beegfs/tmpdir/qchem11608/ 0
/share/apps/common/q-chem/5.2.1/exe/qcprog.exe_s h2_2.75.inp_11608.0 /mnt/beegfs/tmpdir/qchem11608/
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 16:34:39 2021
Host:
0
Scratch files written to /mnt/beegfs/tmpdir/qchem11608//
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 2.75
$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 -1.3750000000
2 H 0.0000000000 0.0000000000 1.3750000000
----------------------------------------------------------------
Molecular Point Group D*h NOp =***
Largest Abelian Subgroup D2h NOp = 1
Nuclear Repulsion Energy = 0.19242808 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) 2.750000
A cutoff of 1.0D-12 yielded 204 shell pairs
There are 2625 function pairs
Smallest overlap matrix eigenvalue = 1.74E-03
Scale SEOQF with 1.000000e+00/1.000000e+00/1.000000e+00
Standard Electronic Orientation quadrupole field applied
Nucleus-field energy = -0.0000000041 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 0.1224527660 7.43e-04
2 -0.9692697692 8.08e-03
3 -0.9705000781 7.84e-03
4 -0.9924789553 2.13e-03
5 -0.9957416040 1.43e-05
6 -0.9957414732 3.23e-05
7 -0.9957424244 1.19e-06
8 -0.9957424253 4.14e-08
9 -0.9957424253 4.51e-09
10 -0.9957424253 1.19e-10 Convergence criterion met
---------------------------------------
SCF time: CPU 1.41s wall 1.00s
<S^2> = 2.000000000
SCF energy in the final basis set = -0.9957424253
Total energy in the final basis set = -0.9957424253
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 0.048097 0.004325
2 0 20 0.001610 0.000169
3 7 13 0.000033 0.000004
4 20 0 0.000001 0.000000 Roots Converged
---------------------------------------------------
---------------------------------------------------
SF-DFT Excitation Energies
(The first "excited" state might be the ground state)
---------------------------------------------------
Excited state 1: excitation energy (eV) = 4.6770
Total energy for state 1: -0.82386666 au
<S**2> : 0.0394
S( 1) --> S( 2) amplitude = -0.4919 alpha
S( 1) --> V( 2) amplitude = 0.1657 alpha
S( 2) --> S( 1) amplitude = 0.8323 alpha
S( 2) --> V( 1) amplitude = 0.1858 alpha
Excited state 2: excitation energy (eV) = 4.9263
Total energy for state 2: -0.81470473 au
<S**2> : 1.9617
S( 1) --> S( 1) amplitude = 0.7184 alpha
S( 1) --> V( 1) amplitude = 0.1779 alpha
S( 2) --> S( 2) amplitude = -0.6413 alpha
S( 2) --> V( 2) amplitude = 0.1935 alpha
Excited state 3: excitation energy (eV) = 9.2888
Total energy for state 3: -0.65438502 au
<S**2> : 0.1883
S( 1) --> S( 1) amplitude = 0.6754 alpha
S( 2) --> S( 2) amplitude = 0.7310 alpha
Excited state 4: excitation energy (eV) = 9.5846
Total energy for state 4: -0.64351664 au
<S**2> : 0.1811
S( 1) --> S( 2) amplitude = 0.8293 alpha
S( 2) --> S( 1) amplitude = 0.5347 alpha
Excited state 5: excitation energy (eV) = 14.5755
Total energy for state 5: -0.46010158 au
<S**2> : 0.9617
S( 1) --> S( 2) amplitude = 0.2441 alpha
S( 1) --> V( 2) amplitude = 0.5431 alpha
S( 2) --> V( 1) amplitude = 0.7855 alpha
Excited state 6: excitation energy (eV) = 14.6022
Total energy for state 6: -0.45912200 au
<S**2> : 1.0285
S( 1) --> S( 1) amplitude = -0.1604 alpha
S( 1) --> V( 1) amplitude = 0.6003 alpha
S( 2) --> S( 2) amplitude = 0.2188 alpha
S( 2) --> V( 2) amplitude = 0.7471 alpha
Excited state 7: excitation energy (eV) = 17.8756
Total energy for state 7: -0.33882450 au
<S**2> : 0.8412
S( 1) --> V( 1) amplitude = 0.7729 alpha
S( 2) --> V( 2) amplitude = -0.6268 alpha
Excited state 8: excitation energy (eV) = 17.8851
Total energy for state 8: -0.33847724 au
<S**2> : 0.8466
S( 1) --> V( 2) amplitude = 0.7000 alpha
S( 2) --> V( 1) amplitude = -0.4842 alpha
S( 2) --> V( 3) amplitude = 0.5096 alpha
Excited state 9: excitation energy (eV) = 18.1254
Total energy for state 9: -0.32964524 au
<S**2> : 0.9897
S( 1) --> V( 2) amplitude = -0.4107 alpha
S( 2) --> V( 1) amplitude = 0.3211 alpha
S( 2) --> V( 3) amplitude = 0.8353 alpha
Excited state 10: excitation energy (eV) = 18.8405
Total energy for state 10: -0.30336677 au
<S**2> : 0.9927
S( 1) --> V( 3) amplitude = 0.9670 alpha
S( 2) --> V( 8) amplitude = -0.2197 alpha
Excited state 11: excitation energy (eV) = 18.8775
Total energy for state 11: -0.30200872 au
<S**2> : 1.0000
S( 1) --> V( 7) amplitude = -0.4539 alpha
S( 2) --> V( 5) amplitude = 0.8902 alpha
Excited state 12: excitation energy (eV) = 18.8775
Total energy for state 12: -0.30200872 au
<S**2> : 1.0000
S( 1) --> V( 6) amplitude = -0.4539 alpha
S( 2) --> V( 4) amplitude = 0.8902 alpha
Excited state 13: excitation energy (eV) = 19.2409
Total energy for state 13: -0.28865077 au
<S**2> : 1.0000
S( 1) --> V( 5) amplitude = 0.7735 alpha
S( 2) --> V( 7) amplitude = -0.6325 alpha
Excited state 14: excitation energy (eV) = 19.2409
Total energy for state 14: -0.28865077 au
<S**2> : 1.0000
S( 1) --> V( 4) amplitude = 0.7735 alpha
S( 2) --> V( 6) amplitude = -0.6325 alpha
Excited state 15: excitation energy (eV) = 22.7927
Total energy for state 15: -0.15812450 au
<S**2> : 1.0000
S( 1) --> V( 5) amplitude = 0.6332 alpha
S( 2) --> V( 7) amplitude = 0.7739 alpha
Excited state 16: excitation energy (eV) = 22.7927
Total energy for state 16: -0.15812450 au
<S**2> : 1.0000
S( 1) --> V( 4) amplitude = 0.6332 alpha
S( 2) --> V( 6) amplitude = 0.7739 alpha
Excited state 17: excitation energy (eV) = 23.1795
Total energy for state 17: -0.14391304 au
<S**2> : 1.0000
S( 1) --> V( 7) amplitude = 0.8904 alpha
S( 2) --> V( 5) amplitude = 0.4547 alpha
Excited state 18: excitation energy (eV) = 23.1795
Total energy for state 18: -0.14391304 au
<S**2> : 1.0000
S( 1) --> V( 6) amplitude = 0.8904 alpha
S( 2) --> V( 4) amplitude = 0.4547 alpha
Excited state 19: excitation energy (eV) = 26.0306
Total energy for state 19: -0.03913639 au
<S**2> : 0.9984
S( 1) --> V( 3) amplitude = 0.2231 alpha
S( 2) --> V( 8) amplitude = 0.9724 alpha
Excited state 20: excitation energy (eV) = 26.8853
Total energy for state 20: -0.00772448 au
<S**2> : 0.9983
S( 1) --> V( 8) amplitude = 0.9806 alpha
S( 2) --> V( 3) amplitude = 0.1816 alpha
---------------------------------------------------
SETman timing summary (seconds)
CPU time 1.01s
System time 0.00s
Wall time 1.26s
--------------------------------------------------------------
Orbital Energies (a.u.)
--------------------------------------------------------------
Alpha MOs
-- Occupied --
-0.4011 -0.3676
-- Virtual --
0.1979 0.2133 0.3244 0.3762 0.3762 0.4309 0.4309 0.5891
0.9827 1.0655 1.6708 1.6708 1.6966 1.7320 1.7320 1.7347
1.9254 1.9254 1.9294 1.9322 1.9326 1.9339 1.9343 1.9533
1.9533 2.1752 2.8757 2.9291 4.2445 4.2445 4.2917 4.2917
4.3502 4.3550 5.8655 5.8655 5.8655 5.8655 5.8656 5.8656
5.8656 5.8656 5.8657 5.8657 5.8658 5.8658 5.8701 5.8775
7.8648 7.8791 7.8791 7.8855 7.8858 7.8866 7.8869 7.8957
7.8957 7.9739 9.3203 9.3544 9.4485 9.4485 9.4693 9.4693
9.4981 9.5114 22.1841 22.3413
--------------------------------------------------------------
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 -2.7385 XY 0.0000 YY -2.7385
XZ -0.0000 YZ 0.0000 ZZ -2.9080
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 -3.5414 XXXY 0.0000 XXYY -1.1805
XYYY 0.0000 YYYY -3.5414 XXXZ -0.0000
XXYZ 0.0000 XYYZ -0.0000 YYYZ 0.0000
XXZZ -6.4575 XYZZ 0.0000 YYZZ -6.4575
XZZZ -0.0000 YZZZ 0.0000 ZZZZ -35.6103
-----------------------------------------------------------------
Archival summary:
1\1\lcpq-curie.ups-tlse.fr\SP\ProcedureUnspecified\BasisUnspecified\2(3)\emonino\FriJan2216:34:422021FriJan2216:34:422021\0\\#,ProcedureUnspecified,BasisUnspecified,\\0,3\H\H,1,2.75\\\@
Total job time: 2.99s(wall), 2.53s(cpu)
Fri Jan 22 16:34:42 2021
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