“…Interferometric scattering microscopy (iSCAT) − is a simple bright-field imaging technique that records the interference (Re[ E scat * E refl ] = | E scat || E refl | cos Δϕ) between a scattered field ( E scat ) from a NP and a field reflected from the interface between the substrate and medium (water or air) ( E refl ). The phase difference (Δϕ = ϕ scat + Φ Gouy + ϕ refl ) includes the scattering phase shift of the NP relative to the incident field (ϕ scat ), , as well as the phase shift induced by the substrate reflection (ϕ refl ), and the Gouy phase shift − (Φ Gouy ). The technique, which has far greater sensitivity than DFS, − , has been used successfully for NP tracking, ,,,, label-free single-biomolecule detection, − and molecular mass analysis. ,,,, However, iSCAT does not provide a separate amplitude (| E scat |) and intrinsic phase (ϕ scat ) of E scat , making it difficult to extract the quantitative spectroscopic information on the optical scattering of a single NP.…”