Enhancement in Organic Photovoltaics Controlled by the Interplay between Charge-Transfer Excitons and Surface Plasmons.

In this work, we investigate plasmonic enhancement in poly(3-hexylthiophene):phenyl-C61-butyric acid methyl ester organic photovoltaics (OPVs) by integrating shape- and size-controlled bimetallic gold core-silver shell nanocrystals (Au-Ag NCs) into the poly(3,4-ethylenedioxythiophene):polystyrene sulfonate hole-transport layer. We observed that the best-performing Au-Ag NC-incorporated OPVs improved the power conversion efficiency by 9% via a broadband increase in photocurrent throughout the visible spectrum. Our experimental and computational results suggest that the observed photocurrent enhancement in plasmonic OPVs originates from both enhanced absorption and improved exciton dissociation and charge collection. This is particularly achieved by placing metal NCs near the interface of the active layer and hole-transport layer. The impedance spectroscopy results suggest that Au-Ag NCs reduce recombination and also increase the internal exciton to carrier efficiency by driving the dissociation of bound charge-transfer states to free carriers.

Plasmonic effects in ultrathin amorphous silicon solar cells: performance improvements with Ag nanoparticles on the front, the back, and both.

Thin-film hydrogenated amorphous silicon (a-Si:H) solar cells that are free-standing over a 2x2 mm area have been fabricated with thicknesses of 150 nm, 100 nm, and 60 nm. Silver nanoparticles (NPs) created on the front and/or back surfaces of the solar cells led to improvement in performance measures such as current density, overall efficiency, and external quantum efficiency. The effect of changing silver nanoparticle size and incident light angle was tested. Finite-Difference Time-Domain simulations are presented as a way to understand the experimental results as well as guide future research efforts.