Exploring systematic discrepancies in DFT calculations of chlorine nuclear quadrupole couplings
Previous studies have revealed significant discrepancies between density functional theory (DFT)-calculated and experimental nuclear quadrupolar coupling constants (CQ) for chlorine atoms, particularly in ionic solids. Various aspects of the computations are systematically investigated here, includi...
| Main Authors: | , , , , |
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| Format: | Journal article |
| Jezik: | English |
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American Chemical Society
2017
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| _version_ | 1826257864032780288 |
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| author | Socha, O Hodgkinson, P Widdifield, C Yates, J Dračínský, M |
| author_facet | Socha, O Hodgkinson, P Widdifield, C Yates, J Dračínský, M |
| author_sort | Socha, O |
| collection | OXFORD |
| description | Previous studies have revealed significant discrepancies between density functional theory (DFT)-calculated and experimental nuclear quadrupolar coupling constants (CQ) for chlorine atoms, particularly in ionic solids. Various aspects of the computations are systematically investigated here, including the choice of the DFT functional, basis set convergence, and geometry optimization protocol. The effects of fast (fs) time-scale dynamics are probed using molecular dynamics (MD) and nuclear quantum effects (NQEs) are considered using path-integral MD calculations. It is shown that the functional choice is the most important factor related to improving the accuracy of the quadrupolar coupling calculations, and that functionals beyond the generalized gradient approximation (GGA) level, such as hybrid and meta-GGA functionals, are required for good correlations with experiment. The influence of molecular dynamics and NQEs is less important than the functional choice in the studied systems. A method which involves scaling the calculated quadrupolar coupling constant is proposed here; its application leads to good agreement with experimental data. |
| first_indexed | 2024-03-06T18:24:54Z |
| format | Journal article |
| id | oxford-uuid:079d8817-de93-49cb-b4b5-337658efe2ca |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-06T18:24:54Z |
| publishDate | 2017 |
| publisher | American Chemical Society |
| record_format | dspace |
| spelling | oxford-uuid:079d8817-de93-49cb-b4b5-337658efe2ca2022-03-26T09:08:28ZExploring systematic discrepancies in DFT calculations of chlorine nuclear quadrupole couplingsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:079d8817-de93-49cb-b4b5-337658efe2caEnglishSymplectic Elements at OxfordAmerican Chemical Society2017Socha, OHodgkinson, PWiddifield, CYates, JDračínský, MPrevious studies have revealed significant discrepancies between density functional theory (DFT)-calculated and experimental nuclear quadrupolar coupling constants (CQ) for chlorine atoms, particularly in ionic solids. Various aspects of the computations are systematically investigated here, including the choice of the DFT functional, basis set convergence, and geometry optimization protocol. The effects of fast (fs) time-scale dynamics are probed using molecular dynamics (MD) and nuclear quantum effects (NQEs) are considered using path-integral MD calculations. It is shown that the functional choice is the most important factor related to improving the accuracy of the quadrupolar coupling calculations, and that functionals beyond the generalized gradient approximation (GGA) level, such as hybrid and meta-GGA functionals, are required for good correlations with experiment. The influence of molecular dynamics and NQEs is less important than the functional choice in the studied systems. A method which involves scaling the calculated quadrupolar coupling constant is proposed here; its application leads to good agreement with experimental data. |
| spellingShingle | Socha, O Hodgkinson, P Widdifield, C Yates, J Dračínský, M Exploring systematic discrepancies in DFT calculations of chlorine nuclear quadrupole couplings |
| title | Exploring systematic discrepancies in DFT calculations of chlorine nuclear quadrupole couplings |
| title_full | Exploring systematic discrepancies in DFT calculations of chlorine nuclear quadrupole couplings |
| title_fullStr | Exploring systematic discrepancies in DFT calculations of chlorine nuclear quadrupole couplings |
| title_full_unstemmed | Exploring systematic discrepancies in DFT calculations of chlorine nuclear quadrupole couplings |
| title_short | Exploring systematic discrepancies in DFT calculations of chlorine nuclear quadrupole couplings |
| title_sort | exploring systematic discrepancies in dft calculations of chlorine nuclear quadrupole couplings |
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