Choosing an atomic basis set for TD-DFT, SOPPA, ADC(2), CIS(D), CC2 and EOM-CCSD calculations of low-lying excited states of organic dyes

Verfasser / Beitragende:
[Adèle Laurent, Aymeric Blondel, Denis Jacquemin]
Ort, Verlag, Jahr:
2015
Enthalten in:
Theoretical Chemistry Accounts, 134/6(2015-06-01), 1-11
Format:
Artikel (online)
ID: 605487251
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024 7 0 |a 10.1007/s00214-015-1676-9  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00214-015-1676-9 
245 0 0 |a Choosing an atomic basis set for TD-DFT, SOPPA, ADC(2), CIS(D), CC2 and EOM-CCSD calculations of low-lying excited states of organic dyes  |h [Elektronische Daten]  |c [Adèle Laurent, Aymeric Blondel, Denis Jacquemin] 
520 3 |a Aiming to pinpoint an atomic basis set providing accurate transition energies at a minimal computational cost, we investigate the evolution with basis set size of the energy of low-lying excited states in nine representative conjugated dyes with a wide panel of theoretical approaches, namely TD-DFT, SOPPA, ADC(2), CIS(D), CC2, EOM-CCSD, as well as several scaled opposite spin variants, namely SOS-CIS(D), SOS-CIS(D0) and SOS-ADC(2). At the exception of TD-DFT that displays the lowest basis set dependence, it turns out that the changes obtained when increasing the size of the basis set are rather independent of the selected wavefunction model, but strongly change according to the nature of the excited state considered. Reasonable compromises between accuracy and computational burden can be attained with 6-311+G(2d,p) that allows much faster calculations than the typical reference basis set, namely aug-cc-pVTZ, for an average loss of accuracy limited to ca. 0.02eV. 
540 |a Springer-Verlag Berlin Heidelberg, 2015 
690 7 |a TD-DFT  |2 nationallicence 
690 7 |a ADC  |2 nationallicence 
690 7 |a EOM-CC  |2 nationallicence 
690 7 |a CIS(D )  |2 nationallicence 
690 7 |a Basis set  |2 nationallicence 
700 1 |a Laurent  |D Adèle  |u Laboratoire CEISAM - UMR CNRS 6230, Université de Nantes, 2 Rue de la Houssinière, BP 92208, 44322, Nantes Cedex 3, France  |4 aut 
700 1 |a Blondel  |D Aymeric  |u Laboratoire CEISAM - UMR CNRS 6230, Université de Nantes, 2 Rue de la Houssinière, BP 92208, 44322, Nantes Cedex 3, France  |4 aut 
700 1 |a Jacquemin  |D Denis  |u Laboratoire CEISAM - UMR CNRS 6230, Université de Nantes, 2 Rue de la Houssinière, BP 92208, 44322, Nantes Cedex 3, France  |4 aut 
773 0 |t Theoretical Chemistry Accounts  |d Springer Berlin Heidelberg  |g 134/6(2015-06-01), 1-11  |x 1432-881X  |q 134:6<1  |1 2015  |2 134  |o 214 
856 4 0 |u https://doi.org/10.1007/s00214-015-1676-9  |q text/html  |z Onlinezugriff via DOI 
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900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
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949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00214-015-1676-9  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Laurent  |D Adèle  |u Laboratoire CEISAM - UMR CNRS 6230, Université de Nantes, 2 Rue de la Houssinière, BP 92208, 44322, Nantes Cedex 3, France  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Blondel  |D Aymeric  |u Laboratoire CEISAM - UMR CNRS 6230, Université de Nantes, 2 Rue de la Houssinière, BP 92208, 44322, Nantes Cedex 3, France  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Jacquemin  |D Denis  |u Laboratoire CEISAM - UMR CNRS 6230, Université de Nantes, 2 Rue de la Houssinière, BP 92208, 44322, Nantes Cedex 3, France  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Theoretical Chemistry Accounts  |d Springer Berlin Heidelberg  |g 134/6(2015-06-01), 1-11  |x 1432-881X  |q 134:6<1  |1 2015  |2 134  |o 214