Relativistic Linear Response in Quantum-Electrodynamical Density Functional Theory
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arXiv
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| Auteurs principaux: | , , , , |
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| Format: | Preprint |
| Publié: |
2024
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| _version_ | 1866929412666032128 |
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| author | Konecny, Lukas Kosheleva, Valeriia P. Appel, Heiko Ruggenthaler, Michael Rubio, Angel |
| author_facet | Konecny, Lukas Kosheleva, Valeriia P. Appel, Heiko Ruggenthaler, Michael Rubio, Angel |
| contents | We present the theoretical derivation and numerical implementation of the linear response equations for relativistic quantum electrodynamical density functional theory (QEDFT). In contrast to previous works based on the Pauli-Fierz Hamiltonian, our approach describes electrons interacting with photonic cavity modes at the four-component Dirac-Kohn-Sham level, derived from fully relativistic QED through a series of established approximations. Moreover, we show that a new type of spin-orbit-like (SO) cavity-mediated interaction appears under the relativistic description of the coupling of matter with quantized cavity modes. Benchmark calculations performed for atoms of group 12 elements (Zn, Cd, Hg) demonstrate how a relativistic treatment enables the description of exciton polaritons which arise from the hybridization of formally forbidden singlet-triplet transitions with cavity modes. For atoms in cavities tuned on resonance with a singlet-triplet transition we discover a significant interplay between SO effects and coupling to an off-resonant intense singlet-singlet transition. This dynamic relationship highlights the crucial role of ab initio approaches in understanding cavity quantum electrodynamics. Finally, using the mercury porphyrin complex as an example, we show that relativistic linear response QEDFT provides computationally feasible first-principles calculations of polaritonic states in large heavy element-containing molecules of chemical interest. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2407_02441 |
| institution | arXiv |
| publishDate | 2024 |
| record_format | arxiv |
| spellingShingle | Relativistic Linear Response in Quantum-Electrodynamical Density Functional Theory Konecny, Lukas Kosheleva, Valeriia P. Appel, Heiko Ruggenthaler, Michael Rubio, Angel Chemical Physics We present the theoretical derivation and numerical implementation of the linear response equations for relativistic quantum electrodynamical density functional theory (QEDFT). In contrast to previous works based on the Pauli-Fierz Hamiltonian, our approach describes electrons interacting with photonic cavity modes at the four-component Dirac-Kohn-Sham level, derived from fully relativistic QED through a series of established approximations. Moreover, we show that a new type of spin-orbit-like (SO) cavity-mediated interaction appears under the relativistic description of the coupling of matter with quantized cavity modes. Benchmark calculations performed for atoms of group 12 elements (Zn, Cd, Hg) demonstrate how a relativistic treatment enables the description of exciton polaritons which arise from the hybridization of formally forbidden singlet-triplet transitions with cavity modes. For atoms in cavities tuned on resonance with a singlet-triplet transition we discover a significant interplay between SO effects and coupling to an off-resonant intense singlet-singlet transition. This dynamic relationship highlights the crucial role of ab initio approaches in understanding cavity quantum electrodynamics. Finally, using the mercury porphyrin complex as an example, we show that relativistic linear response QEDFT provides computationally feasible first-principles calculations of polaritonic states in large heavy element-containing molecules of chemical interest. |
| title | Relativistic Linear Response in Quantum-Electrodynamical Density Functional Theory |
| topic | Chemical Physics |
| url | https://arxiv.org/abs/2407.02441 |