A metal nanoparticle much smaller than the light wavelength supports a localized surface plasmon resonance (LSPR): its free electrons oscillate collectively against the ionic core when driven by an incident field. In the quasistatic dipole (Fröhlich) approximation, resonance occurs when
Re[ε_metal(λ)] = −2 ε_host
Drude model: ε_metal(λ) ≈ 1 − (λ/λp)²
⇒ λ_res = λp · √(1 + 2 ε_host), ε_host = n_host²
λp is the metal's bulk plasma wavelength (≈135 nm Ag, ≈137 nm Au, ≈141 nm Cu in this simplified free-electron model, which ignores interband transitions). Embedding the nanoparticles in a higher-index semiconductor pushes λ_res deep into the visible/near-IR — exactly why plasmonic light-trapping layers are built directly on the absorber.
Near resonance, a nanoparticle scatters incident light at large angles rather than letting it pass straight through. In a thin film that is normally too thin to fully absorb long-wavelength light, this redirected, path-lengthened light has far more chance of being absorbed before it reaches the back contact — a real strategy used to cut absorber-layer thickness in thin-film photovoltaics (Atwater & Polman, Nat. Mater. 2010).
- Material — sets the metal's plasma wavelength λp.
- Host index n — the surrounding dielectric/semiconductor; raising it red-shifts λ_res.
- Wavelength — the monochromatic beam's photon wavelength; watch photons scatter sideways into the film only near resonance.
- Size/coverage — larger, denser nanoparticles have a bigger scattering cross-section, raising the peak coupling probability.
The bare-film baseline uses a simplified Beer–Lambert absorptance 1 − e−α(λ)t with α falling toward longer wavelengths, modelling a weakly-absorbing near-band-edge film — the regime where plasmonic trapping helps most.