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This study establishes the relationships between the structure of a series of meso-substituted tin­(IV) porphyrins and their efficiency as photosensitizers for hydrogen generation in the Sn­(IV)­P/Pt–TiO2 nanocomposite system. The electrochemical properties of a series of SnPs, the catalytic performance of Pt nanomodifications, and the morphology of the Pt/TiO2 nanocomposites were characterized by electrochemical and electron microscopy methods. The dependence of photocatalytic performance on the structure for a series of Sn­(IV) meso-substituted phenyl porphyrins was studied, and possible mechanisms are discussed employing the results of the electrochemical studies. It was found that the time course and type of the photochemically reduced species of Sn­(IV)­Ps, which are essential intermediates, are important factors and depend on the electronegativity of the metal center, the character of meso-substituents of the porphyrin ring, and pH and are correlated with the redox potential sequence of the respective Sn­(IV)­Ps: SnTMPyP > SnTPyP > SnTPPS > SnTPPC. Optimization of the experimental parameters was performed with regard to the SnPs with different functional groups, pH values, concentrations of Pt/TiO2, light intensity, and Pt nanoparticles with different surface stabilizers. Finally, the maximum hydrogen yield under visible light was obtained from the system of Sn­(IV) meso-tetra­(4-pyridyl)­porphyrin dichloride (SnTPyP) sensitized TiO2/Pt prepared by the citrate method/EDTA at pH 9.0. This demonstrates that the photochemically reduced species of SnTPyP are relatively long lived, so they have enough time to complete electron transfer to TiO2 and/or Pt. The adsorption of SnTPyP on the TiO2/Pt surface is therefore not essential for hydrogen generation. Moreover, this study demonstrates for the first time the synergic effect of the excitation of TiO2 and mostly Q-bands of Sn­(IV)P (wavelength range 390–650 nm), which enhances the efficiency of photocatalytic hydrogen generation in the system. The Soret band of Sn­(IV)­TPyP was found to produce a minor (about 23%) contribution to the photocatalytic activity of the porphyrin sensitizer in this system. Possible processes involved are discussed, and mechanisms are proposed explaining different aspects of a series of photocatalytic systems with SnPs and Pt catalysts for hydrogen production under visible light. These structure–function relationships are essential to effectively harness solar energy for hydrogen production as well as for a wide range of energy and environmentally related problems.

Methods to prepare ultrathin gold nanowires and monodisperse nanoparticles based on the intrinsic property of gold(I) ions to form aurophilic interactions stabilized by oleylamine and long-chain alkylamine have been widely explored. Due to the low thermodynamic stability of the high aspect ratio nanostructures, their conjugation and assembly into functional nanosystems have not been explored so far. One of the reasons for this is that the surface of the nanostructures is insulated by stabilization compounds, which preserve the integrity of the nanostructures but at the same time form an insulating barrier in electronic and electrochemical systems in contact areas and for the charge transfer reactions. Conjugation of a metalloprotein cytochrome c (Cyt c) with oleylamine-stabilized gold ultrathin nanowires and nanoparticles into a bioelectrochemically active nanoarchitecture is presented here for the first time. Methods of preparing and assembling the ultrathin nanowires and nanoparticles on the thin-film gold electrodes are shown. Thermodynamic and kinetic parameters were obtained for the direct electron transfer reaction of cyt c on these surfaces. Nanowires are responsible for an approximately −20 mV shift in the redox potential of the ferri/ferro-cyt c couple relative to a thin-film gold electrode.

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