Accuracy of Charge Densities in Electronic Structure Calculations
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arXiv
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| Autores principales: | , , , |
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| Formato: | Preprint |
| Publicado: |
2024
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| _version_ | 1866916648988966912 |
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| author | Gubler, Moritz Schäfer, Moritz R. Behler, Jörg Goedecker, Stefan |
| author_facet | Gubler, Moritz Schäfer, Moritz R. Behler, Jörg Goedecker, Stefan |
| contents | Accurate charge densities are essential for reliable electronic structure calculations because they significantly impact predictions of various chemical properties and in particular, according to the Hellmann-Feynman theorem, atomic forces. This study examines the accuracy of charge densities obtained from different DFT exchange-correlation functionals in comparison with coupled cluster calculations with single and double excitations. We find that modern DFT functionals can provide highly accurate charge densities, particularly in case of meta-GGA and hybrid functionals. In connection with Gaussian basis sets, it is necessary to use the largest basis sets available to obtain densitites that are nearly basis set error free. These findings highlight the importance of selecting appropriate computational methods for generating high-precision charge densities, which are for instance needed to generate reference data for training modern machine learned potentials. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2410_17866 |
| institution | arXiv |
| publishDate | 2024 |
| record_format | arxiv |
| spellingShingle | Accuracy of Charge Densities in Electronic Structure Calculations Gubler, Moritz Schäfer, Moritz R. Behler, Jörg Goedecker, Stefan Chemical Physics Accurate charge densities are essential for reliable electronic structure calculations because they significantly impact predictions of various chemical properties and in particular, according to the Hellmann-Feynman theorem, atomic forces. This study examines the accuracy of charge densities obtained from different DFT exchange-correlation functionals in comparison with coupled cluster calculations with single and double excitations. We find that modern DFT functionals can provide highly accurate charge densities, particularly in case of meta-GGA and hybrid functionals. In connection with Gaussian basis sets, it is necessary to use the largest basis sets available to obtain densitites that are nearly basis set error free. These findings highlight the importance of selecting appropriate computational methods for generating high-precision charge densities, which are for instance needed to generate reference data for training modern machine learned potentials. |
| title | Accuracy of Charge Densities in Electronic Structure Calculations |
| topic | Chemical Physics |
| url | https://arxiv.org/abs/2410.17866 |