Abstract
Electromagnetic response is commonly computed in two languages: length-gauge molecular polarizabilities and velocity-gauge (Kubo) conductivities for periodic solids. We introduce a compact, gauge-invariant bridge that carries the same microscopic inputs—transition dipoles and interaction kernels—from molecules to crystals and heterogeneous media, with explicit SI prefactors and fine-structure scaling via α fs. The long-wavelength limit is handled through a reduced dielectric matrix that retains local-field mixing; interfaces and 2D layers are treated with sheet boundary conditions (rather than naïve ultrathin films); and length–velocity equivalence is enforced in practice by including the equal-time (diamagnetic/contact) term alongside the paramagnetic current. Finite temperature is addressed on the Matsubara axis with numerically stable real-axis evaluation (complex polarization propagator), preserving unit consistency end-to-end. The framework enables predictive, unit-faithful observables from radio frequency to ultraviolet—RF/microwave heating and penetration depth, dielectric-logging contrast, interfacial optics of thin films and 2D sheets, and adsorption metrics via imaginary-axis polarizabilities. Numerical checks (gauge overlay and optical f-sum saturation) validate the implementation. Immediate priorities include compact, temperature- and salinity-aware kernels with quantified uncertainties and operando interfacial diagnostics for integration into multiphysics digital twins.
| Original language | English |
|---|---|
| Article number | 024108 |
| Journal | The Journal of Chemical Physics |
| Volume | 164 |
| Issue number | 2 |
| DOIs | |
| State | Published - 14 Jan 2026 |
Bibliographical note
Publisher Copyright:© 2026 Author(s).
ASJC Scopus subject areas
- General Physics and Astronomy
- Physical and Theoretical Chemistry
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