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Photoelectrochemical water splitting can be regarded as a promising technology for renewable hydrogen production. In the current work, a facile hydrothermal synthesis method was used to directly grow TiO2 flower-like structures/TiO2 nanorods on a conductive glass substrate. Moreover, three different gold deposition methods, namely, a photoreduction method (PR), the Turkevich method (TK) and a combination of both methods (CM), were applied to decorate the formed flower-like structures with gold nanoparticles (GNPs). The type of deposition technique affected the size, size distribution, loading, surface coverage and shape of the obtained GNPs. With the PR technique, the photocurrent increased 3.5-fold compared to that of the bare flower-like structures. With the TK method, a narrow GNP distribution was obtained, yielding a 6.15-fold increase in photocurrent. Using the CM approach, a 1.21-, 26.86- and 12.79-fold increase was observed for current density compared to that of the corresponding bare samples. All samples showed stable chronoamperometric performance under illumination without any signs of photocorrosion or performance deterioration. Electrochemical impedance spectroscopy showed that the CM approach decreased the semiconductor/electrolyte interfacial resistance to 37, 2.5 and 3.1% of the values for the bare samples. Bode phase plots showed that the stacked flower-like structures can be considered electron-hole recombination centres, leading to an observable broadening of the maximum-frequency peak.

Results reported in this research paper are related to the photo-oxidation of water into molecular oxygen, using n-type photoelectrodes operated with the support of an external electric bias. These photoanodes are made of 1 cm2 rectangular glass substrates, surface-covered by thin films of conductive fluorine-doped tin oxide (FTO). Thin mats of titanium dioxide nanorods (TDNRs) have been deposited over the FTO surfaces. The TDNRs have then been sensitized by surface deposition of cobalt dodecahedral Zeolitic Imidazolate Framework (ZIF-67) metal organic framwork (MOF). ZIF-67 has been deposited using a two-step process: (i) deposition of cobalt hydroxide by chronoamperometry; (ii) in-situ transformation of cobalt hydroxide into ZIF-67 by chemical reaction with a solution of 2-methylimidazol. The amount of ZIF-67 has been adjusted by monitoring the duration of the electro-reduction step. The photoanodes have been characterized by scanning electron microscopy, X-ray diffraction spectroscopy, X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy, and UV–Vis absorption spectroscopy. The photoelectrochemical responses of the different photoanodes have been measured under chopped illumination conditions. Dark currents as high as 100–150 μA/cm2 and photocurrents of only 10–15 μA/cm2 have been measured on fresh samples with large MOF contents, at an operating potential of +1.0 V vs. saturated calomel electrode, 25 °C, under UV–Vis irradiation. No dark current and photocurrents close to 40 μA/cm2 have been measured on samples with low MOF contents. The dynamics of charge transfer leading to the formation of molecular oxygen has been analyzed by photoelectrochemical impedance spectroscopy to understand the interplay between the OER electroactivity and photoelectroactivity. It is shown that large MOF contents induce two contradictory effects: the first one (faster charge transfer kinetics) is desirable while the second one (faster charge recombination kinetics) is not desirable. Only limited MOF contents are beneficial to maximize the photocurrent density.