Spin-Orbit Induced Non-Adiabatic Dynamics: An Exact $Ω$-Representation
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arXiv
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| Auteurs principaux: | , |
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| Format: | Preprint |
| Publié: |
2026
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| _version_ | 1866911498048110592 |
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| author | Brady, Ryan P. Yurchenko, Sergei N. |
| author_facet | Brady, Ryan P. Yurchenko, Sergei N. |
| contents | Transforming rovibronic Hamiltonians of molecular systems from the $ΛS$ (Hund's case a) basis to the adiabatic $Ω$ representation is widely used to "remove" spin-orbit coupling (SOC) and enable single-state treatments of spectra and dynamics. We show that this simplification is only apparent: the SOC elimination necessarily generates sizeable non-adiabatic couplings (NACs) from the nuclear kinetic energy operator. Neglecting these spin-orbit-induced NACs causes severe errors in rovibronic energies and transition properties. Using an analytically tractable two electronic state model and high-accuracy variational benchmarks, we derive the exact conditions for numerical equivalence between $Ω$ and $ΛS$ formulations and quantify how missing NAC terms and bond-length-dependent spin factors degrade predictions. We implement a complete $Ω$-representation workflow in Duo for diatomics, fully transforming all Hamiltonian terms and enabling side-by-side $Ω$ vs $ΛS$ calculations. For common single-state pipelines (e.g., LEVEL), we provide diagnostics that flag unsafe regimes and practical remedies to restore accuracy. The results deliver actionable guidance for spectroscopy, photophysics, and kinetics: $Ω$-based single-state approximations are reliable only when interacting states are well separated in the Franck-Condon region; otherwise, explicit non-adiabatic terms are required - even for "forbidden" transitions. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2603_06306 |
| institution | arXiv |
| publishDate | 2026 |
| record_format | arxiv |
| spellingShingle | Spin-Orbit Induced Non-Adiabatic Dynamics: An Exact $Ω$-Representation Brady, Ryan P. Yurchenko, Sergei N. Chemical Physics Computational Physics Transforming rovibronic Hamiltonians of molecular systems from the $ΛS$ (Hund's case a) basis to the adiabatic $Ω$ representation is widely used to "remove" spin-orbit coupling (SOC) and enable single-state treatments of spectra and dynamics. We show that this simplification is only apparent: the SOC elimination necessarily generates sizeable non-adiabatic couplings (NACs) from the nuclear kinetic energy operator. Neglecting these spin-orbit-induced NACs causes severe errors in rovibronic energies and transition properties. Using an analytically tractable two electronic state model and high-accuracy variational benchmarks, we derive the exact conditions for numerical equivalence between $Ω$ and $ΛS$ formulations and quantify how missing NAC terms and bond-length-dependent spin factors degrade predictions. We implement a complete $Ω$-representation workflow in Duo for diatomics, fully transforming all Hamiltonian terms and enabling side-by-side $Ω$ vs $ΛS$ calculations. For common single-state pipelines (e.g., LEVEL), we provide diagnostics that flag unsafe regimes and practical remedies to restore accuracy. The results deliver actionable guidance for spectroscopy, photophysics, and kinetics: $Ω$-based single-state approximations are reliable only when interacting states are well separated in the Franck-Condon region; otherwise, explicit non-adiabatic terms are required - even for "forbidden" transitions. |
| title | Spin-Orbit Induced Non-Adiabatic Dynamics: An Exact $Ω$-Representation |
| topic | Chemical Physics Computational Physics |
| url | https://arxiv.org/abs/2603.06306 |