Abstract
Truncated octahedral gold (Au) nanoparticles (NPs), Au nanocubes (NCs)-, and silver (Ag) NCs are used to study the effect of NPs shape, material and incorporation location on the performance of poly(3-hexylthiophene):[6,6]-phenyl-C(71)-butyric acid methyl ester (P3HT:PC(71)BM) based inverted bulk heterojunction (BHJ) organic solar cells (OSCs). Plasmonic OSCs (POSCs) with NPs incorporated as an interfacial layer between zinc oxide (ZnO) and active layer showed highest power conversion efficiency (PCE) and short circuit current density (J (sc)) values for all kind of shapes and material compared to POSCs with NPs blended into the active layer. Near-field enhancement as well as enhanced forward scattering cross section is attributed for POSC performance improvement. Among the NPs with two shapes, POSCs with truncated octahedral Au NPs exceeded the photovoltaic performance compared to those of POSCs with Au and Ag NCs. Large number of antennas in truncated octahedral Au NPs compared to NC is reasoned to be the cause for this improvement. Even though Ag has better localised surface plasmon resoanance (LSPR) properties compared to Au, the POSCs with Ag NCs showed lower J (sc) value and is due to reduced number of photons at the blue shifted LSPR wavelength of Ag NCs. The improvement in J (sc) values of POSCs is confirmed by enhancement in absorption, external quantum efficiency (EQE), exciton generation and exciton dissociation probability measurements and is due to improved LSPR coupling of the NPs with the active layer. The surface enhanced Raman scattering (SERS) and photoluminescence (PL) studies confirm the absorption enhancement in the active layer by NP LSPR coupling and further confirm the enhancement in the photovoltaic performance of POSCs.