Control of Dye Aggregation and Electron Injection for Highly Efficient Porphyrin Sensitizers Adsorbed on Semiconductor Films with Varying Ratios of Coadsorbate

Abstract

We report the photovoltaic performances and kinetics of femtosecond fluorescence for three zinc-porphyrin sensitizers (YD0−YD2) coadsorbed with chenodeoxycholic acid (CDCA) at three molar ratios on nanocrystalline semiconductor (TiO2 or Al2O3) films. The addition of CDCA improved the efficiencies of YD0 and YD1 so that their maximum performance occurred at a dye/CDCA ratio of 1:2, but the presence of CDCA had a negative effect for YD2. Porphyrin aggregation on TiO2 surfaces not only accelerates the rate of intermolecular energy transfer but also increases the rate of interfacial electron injection, so that the electron injection yields (Φinj) are balanced by these two important factors. As a result, Φinj increased slightly with increasing amount of CDCA for both YD0 and YD1, but decreased for YD2; for this reason, the presence of CDCA failed to improve the photovoltaic performance for YD2, unlike for YD0 and YD1. The cell performances were optimized on TiO2 films of ∼10-μm thickness with a scattering layer of ∼4-μm thickness: the efficiencies of power conversion of YD1 and YD2 are slightly smaller than, but near, that of N719, being 6.5% and 6.8%, respectively, compared to 7.3%. Without a scattering layer on the films, the performance of N719 was degraded significantly (6.3%), whereas the efficiencies of YD1 and YD2 decreased only slightly (6.4% and 6.6%), making this series of green sensitizers promising candidates for future light-penetrable photovoltaic applications.