Highlights Spectroscopic Ellipsometry results showed plasmonic excitations with increased intensity as the average particle diameter increases. Scattering studies showed that the incorporation of Ag NPs enhances the non-specular reflectivity due to the scattering of light; the scattering is maximized and is not strongly affected by the angle of incidence. The resistivity of the hybrid layers is lower in relation to the single PEDOT:PSS sample.
AbstractWe compare the performance of a typical (for use as a hole transport layer in organic photovoltaics) PEDOT:PSS thin film [Poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate)] with a series of PEDOT:PSS layers doped with silver nanoparticles (NPs) of various size distributions. These hybrid layers have attracted great attention as buffer layers in plasmonic organic photovoltaics (OPV), although there is no report up today on their isolated performance. In the present study we prepared a series of PEDOT:PSS layers sandwiched between ITO and Au electrodes. Ag NPs were deposited on top of the ITO by e-beam evaporation followed by the spin coating of PEDOT:PSS. Electrical characterization, under dark, showed linear resistive behavior for all the samples; lower resistance was observed for the hybrid ones. The resistivity decreases as the NPs size increases; preferential current paths formed in PEDOT:PSS through Ag NPs increase substantially the electric field between the ITO and the Au electrodes. A striking observation is the slight change in the inclination of the I-V curves when measured under illumination for the case of the plasmonic layers; an indication that changes in the electric field in the vicinity of the NP due to plasmonic excitation is a non-vanishing factor.