A General and Transferable Local Hybrid Functional for Electronic Structure Theory and Many-Fermion Approaches
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arXiv
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| Format: | Preprint |
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2024
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| _version_ | 1866912191407456256 |
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| author | Holzer, Christof Franzke, Yannick J. |
| author_facet | Holzer, Christof Franzke, Yannick J. |
| contents | Density functional theory has become the workhorse of quantum physics, chemistry, and materials science. Within these fields, a broad range of applications needs to be covered. These applications range from solids to molecular systems, from organic to inorganic chemistry, or even from electrons to other fermions such as protons or muons. This is emphasized by the plethora of density functional approximations that have been developed for various cases. In this work, a new local hybrid exchange-correlation density functional is constructed from first principles, promoting generality and transferability. We show that constraint satisfaction can be achieved even for admixtures with full exact exchange, without sacrificing accuracy. The performance of the new functional for electronic structure theory is assessed for thermochemical properties, excitation energies, Mössbauer isomer shifts, NMR spin--spin coupling constants, NMR shieldings and shifts, magnetizabilities, as well as EPR hyperfine coupling constants. Here, the new density functional shows excellent performance throughout all tests and is numerically robust only requiring small grids for converged results. Additionally, the functional can be easily generalized to arbitrary fermions as shown for electron-proton correlation energies. Therefore, we outline that density functionals generated in this way are general purpose tools for quantum mechanical studies. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2407_21727 |
| institution | arXiv |
| publishDate | 2024 |
| record_format | arxiv |
| spellingShingle | A General and Transferable Local Hybrid Functional for Electronic Structure Theory and Many-Fermion Approaches Holzer, Christof Franzke, Yannick J. Chemical Physics Density functional theory has become the workhorse of quantum physics, chemistry, and materials science. Within these fields, a broad range of applications needs to be covered. These applications range from solids to molecular systems, from organic to inorganic chemistry, or even from electrons to other fermions such as protons or muons. This is emphasized by the plethora of density functional approximations that have been developed for various cases. In this work, a new local hybrid exchange-correlation density functional is constructed from first principles, promoting generality and transferability. We show that constraint satisfaction can be achieved even for admixtures with full exact exchange, without sacrificing accuracy. The performance of the new functional for electronic structure theory is assessed for thermochemical properties, excitation energies, Mössbauer isomer shifts, NMR spin--spin coupling constants, NMR shieldings and shifts, magnetizabilities, as well as EPR hyperfine coupling constants. Here, the new density functional shows excellent performance throughout all tests and is numerically robust only requiring small grids for converged results. Additionally, the functional can be easily generalized to arbitrary fermions as shown for electron-proton correlation energies. Therefore, we outline that density functionals generated in this way are general purpose tools for quantum mechanical studies. |
| title | A General and Transferable Local Hybrid Functional for Electronic Structure Theory and Many-Fermion Approaches |
| topic | Chemical Physics |
| url | https://arxiv.org/abs/2407.21727 |