On the calculation of crystal field parameters using Wannier functions
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arXiv
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| Autori principali: | , , , |
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| Natura: | Preprint |
| Pubblicazione: |
2014
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| _version_ | 1866913883164246016 |
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| author | Scaramucci, Andrea Ammann, Jens Spaldin, Nicola A. Ederer, Claude |
| author_facet | Scaramucci, Andrea Ammann, Jens Spaldin, Nicola A. Ederer, Claude |
| contents | We discuss the calculation of crystal field splittings using Wannier functions and show how the ligand field contributions can be separated from the bare Coulomb contribution to the crystal field by constructing sets of Wannier functions incorporating different levels of hybridization. We demonstrate this method using SrVO$_3$ as a generic example of a transition metal oxide. We then calculate trends in the crystal field splitting for two series of hypothetical tetragonally distorted perovskite oxides and discuss the relation between the calculated "electro-static" contribution to the crystal field and the simple point charge model. Finally, we apply our method to the charge disproportionated 5$d$ electron system CsAuCl$_3$. We show that the negative charge transfer energy in this material leads to a reversal of the $p$-$d$ ligand contribution to the crystal field splitting such that the $e_g$ states of the nominally Au$^{3+}$ cation are energetically lower than the corresponding $t_{2g}$ states. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_1405_3804 |
| institution | arXiv |
| publishDate | 2014 |
| record_format | arxiv |
| spellingShingle | On the calculation of crystal field parameters using Wannier functions Scaramucci, Andrea Ammann, Jens Spaldin, Nicola A. Ederer, Claude Materials Science Strongly Correlated Electrons We discuss the calculation of crystal field splittings using Wannier functions and show how the ligand field contributions can be separated from the bare Coulomb contribution to the crystal field by constructing sets of Wannier functions incorporating different levels of hybridization. We demonstrate this method using SrVO$_3$ as a generic example of a transition metal oxide. We then calculate trends in the crystal field splitting for two series of hypothetical tetragonally distorted perovskite oxides and discuss the relation between the calculated "electro-static" contribution to the crystal field and the simple point charge model. Finally, we apply our method to the charge disproportionated 5$d$ electron system CsAuCl$_3$. We show that the negative charge transfer energy in this material leads to a reversal of the $p$-$d$ ligand contribution to the crystal field splitting such that the $e_g$ states of the nominally Au$^{3+}$ cation are energetically lower than the corresponding $t_{2g}$ states. |
| title | On the calculation of crystal field parameters using Wannier functions |
| topic | Materials Science Strongly Correlated Electrons |
| url | https://arxiv.org/abs/1405.3804 |