The effect of the orientation of the porphyrin sensitizer onto the TiO2 surface on the performance of dye-sensitized solar cells (DSSCs) is reported. Free-base and zinc porphyrins bearing a carboxyl anchoring group at the para, meta, or ortho positions of one of the meso-phenyl rings were synthesized for application in Grätzel-type photoelectrochemical cells. The remainder of the meso-phenyl rings was substituted with alkyl chains of different length to visualize any aggregation effects. Absorption and fluorescence studies were performed to characterize and observe spectral coverage of the thirteen newly synthesized porphyrin derivatives. Photoelectrochemical studies were performed after immobilization of porphyrins onto nanocrystalline TiO2 and compared with DSSC constructed using N719 dye as reference. The performance of DSSCs with the porphyrin anchoring at the para or meta position were found to greatly exceed those with the anchoring group in the ortho position. Additionally, cells constructed using zinc porphyrin derivatives outperformed the free-base porphyrin analogs. Better dye regeneration efficiency for the zinc porphyrin derivatives compared to their free-base porphyrin analogs, and for the meta and para derivatives over the ortho derivatives was evaluated from electrochemical impedance spectroscopy studies. Femtosecond transient absorption spectroscopy studies were performed to probe the kinetics of charge injection and charge recombination with respect to the orientation of porphyrin macrocycle on TiO2 surface. The ortho porphyrin derivative with an almost flat orientation to the TiO2 surface revealed fast charge recombination and suggested occurrence of through-space charge transfer. The overall structure-performance trends observed for the present porphyrin DSSCs have been rationalized based on spectral, electrochemical, electrochemical impedance spectroscopy, and transient spectroscopy results.

Effect of positioning of the cyanoacrylic acid anchoring group on ring periphery of phenothiazine dye on the performance of dye-sensitized solar cells (DSSCs) is reported. Two types of dyes, one having substitution on the C-3 aromatic ring (Type 1) and another through the N-terminal (Type 2), have been synthesized for this purpose. Absorption and fluorescence studies have been performed to visualize the effect of substitution pattern on the spectral coverage and electrochemical studies to monitor the tuning of redox levels. B3LYP/6-31G* studies are performed to visualize the frontier orbital location and their significance in charge injection when surface modified on semiconducting TiO₂. New DSSCs have been built on nanocrystalline TiO₂ according to traditional two-electrode Grätzel solar cell setup with a reference cell based on N719 dye for comparison. The lifetime of the adsorbed phenothiazine dye is found to be quenched significantly upon immobilizing on TiO₂ suggesting charge injection from excited dye to semiconducting TiO₂. The performances of the cells are found to be prominent for solar cells made out of Type 1 dyes compared to Type 2 dyes. This trend has been rationalized on the basis of spectral, electrochemical, computational, and electrochemical impedance spectroscopy results.

Mercury (Hg) contamination is a global issue with implications for both ecosystem and human health. In this study, we use a new approach to link Hg exposure to health effects in spotted gar (Lepisosteus oculatus) from Caddo Lake (TX/LA). Previous field studies have reported elevated incidences of macrophage centers in liver, kidney, and spleen of fish with high concentrations of Hg. Macrophage centers are aggregates of specialized white blood cells that form as an immune response to tissue damage, and are considered a general biomarker of contaminant toxicity. We found elevated incidences of macrophage centers in liver of spotted gar and used a new technology for ecotoxicology studies, laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), to colocalize aggregates and Hg deposits within the tissue architecture. We conclude that Hg compromises the health of spotted gar in our study and, perhaps, other fish exposed to elevated concentrations of Hg.

A multilayer Langmuir-Blodgett (LB) film of the self-assembled electron donor-acceptor dyad of Zn phthalocyanine, appended with four long-chain aliphatic ether peripheral substituents, and an imidazole adduct of C60 was prepared and applied as a photoactive material in a photoelectrochemical cell. Changes in the simultaneously recorded surface pressure and surface potential vs area per molecule compression isotherms for Langmuir films of the dyad and, separately, of its components helped to identify phase transitions and mutual interactions of molecules in films. The Brewster angle microscopy (BAM) imaging of the Langmuir films showed circular condensed phase domains of the dyad molecules. The determined area per molecule was lower than that estimated for the dyad and its components, separately. The multilayer LB films of the dyad were transferred onto hydrophobized fluorine-doped tin oxide-coated (FTO) glass slides under different conditions. The presence of both components in the dyad LB films was confirmed with the UV-vis spectroscopy measurements. For the LB films transferred at different surface pressures, the PM-IRRAS measurements revealed that the phthalocyanine macrocycle planes and ether moieties in films were tilted with respect to the FTO surface. The AFM imaging of the LB films indicated formation of relatively uniform dyad LB films. Then, the femtosecond transient absorption spectral studies evidenced photoinduced electron transfer in the LB film. The obtained transient signals corresponding to both Zn(TPPE)(•+) and C60im(•-) confirmed the occurrence of intramolecular electron transfer. The determined rate constants of charge separation, kcs = 2.6 × 10(11) s(-1), and charge recombination, kcr = 9.7 × 10(9) s(-1), indicated quite efficient electron transfer within the film. In the photoelectrochemical studies, either photoanodic or photocathodic current was generated depending on the applied bias potential when the dyad LB film-coated FTO was used as the working electrode and ascorbic acid or methylviologen, respectively, as the charge mediator in an aqueous solution.