No abstract

The effect of chenodeoxycholic acid as a coadsorbent on TiO 2 nanocrystalline solar cells incorporating phthalocyanine sensitizers was studied under various conditions. Adding chenodeoxycholic acid onto TiO 2 nanoparticles not only reduces the adsorption of phthalocyanine sensitizers but also prevents sensitizer aggregation, leading to different photovoltaic performance. The inspection of IPCE and absorption spectra showed that the load of phthalocyanine sensitizers is strongly dependent on the molar concentration of chenodeoxycholic acid coadsorbent. The open circuit voltage of the solar cells with chenodeoxycholic acid coadsorbent increases due to the enhanced electron lifetime in TiO 2 nanoparticles coupled with the band edge shift of TiO 2 to negative potentials.

Dye-sensitized solar cells based on co-sensitization of organic dyes having complementary spectral absorption in the visible region resulted in a panchromatic response, which exhibited 86% incident monochromatic photon-to-current conversion efficiency in the visible region; the optimized cell gave a short circuit current density of 15.5 mA cm(-2), an open circuit voltage of 685 mV and a fill factor of 0.70 corresponding to an overall conversion efficiency of 7.43% under solar simulated light irradiation of 100 mW cm(-2).

Effects of incorporation of acid-treated single-wall carbon nanotubes (a-SWCNs) in TiO(2) film and of anchorage of dye-linked, a-SWCNs (hereafter dye-SWCNs) to the TiO(2)/electrolyte interface on photocurrent-voltage characteristics of dye-sensitized solar cells were studied. Compared with an unmodified cell, the modified cell with the a-SWCNs in TiO(2) film showed a 25% increase in short-circuit photocurrent (J(sc)). The J(sc) increase is correlated with improved connectivity between the a-SWCNs and the TiO(2) particles and with enhanced light scattering by TiO(2) clusters formed in the presence of the a-SWCNs. In the case of anchoring dye-SWCNs to the TiO(2)/electrolyte interface, the open-circuit voltage (V(oc)) increased by as much as 0.1 V, possibly due to the basicity of the TiO(2) surface from NH groups of ethylenediamine moieties of the anchored dye-SWCNs.