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This study presents an effective and the simplest method to substantially improve the photoelectrochemical water-splitting ability of hydrothermally grown ZnO nanorod arrays (NRAs). In the hydrothermal growth of ZnO NRAs, unwanted Zn(OH) species are formed, which act as trapping sites of photoexcited charges. We found that those inherent charge-trapping sites could be annihilated by the desorption of the hydroxyl groups upon vacuum annealing above 200 °C, which resulted in an enhancement of the charge-separation efficiency and photocurrent density. Another drastic increase in the photocurrent density occurred when ZnO NRAs were treated with annealing at higher temperature (700 °C), which can be attributed to the introduced oxygen vacancies acting as shallow donors in the ZnO crystal lattice. The removal of the charge-trapping Zn(OH) and the generation of oxygen vacancies were confirmed by photoluminescence (PL) and XPS analyses. The ZnO NRAs treated by this simple method yield a photocurrent density of 600 μA/cm at 1.23 V under 1 sun illumination, which is 20 times higher than that obtained from as-grown ZnO NRAs. This study presents a highly efficient way of increasing the bulk electric conductivity and photoelectrochemical activity of metal oxide nanorods without requiring the introduction of any extrinsic dopants.

In this work, enhanced light stability of perovskite solar cell (PSC) achieved by the introduction of a core/shell-structured CdS/TiO2 electrode and the related mechanism are reported. By a simple solution-based process (SILAR), a uniform CdS shell was coated onto the surface of a TiO2 layer, suppressing the activation of intrinsic trap sites originating from the oxygen vacancies of the TiO2 layer. As a result, the proposed CdS-PSC exhibited highly improved light stability, maintaining nearly 80% of the initial efficiency after 12 h of full sunlight illumination. From the X-ray diffraction analyses, it is suggested that the degradation of the efficiency of PSC during illumination occurs regardless of the decomposition of the perovskite absorber. Considering the light-soaking profiles of the encapsulated cells and the OCVD characteristics, it is likely that the CdS shell had efficiently suppressed the undesirable electron kinetics, such as trapping at the surface defects of the TiO2 and preventing the resultant charge losses by recombination. This study suggests that further complementary research on various effective methods for passivation of the TiO2 layer would be highly meaningful, leading to insight into the fabrication of PSCs stable to UV-light for a long time.

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Among three polymorphs of TiO, the brookite is the least known phase in many aspects of its properties and photoactivities (especially comparable to anatase and rutile) because it is the rarest phase to be synthesized in the standard environment among the TiO polymorphs. In this study, we address the unrevealed photocatalytic properties of pure brookite TiO film as an environmental photocatalyst. Highly crystalline brookite nanostructures were synthesized on titanium foil using a well-designed hydrothermal reaction, without harmful precursors and selective etching of anatase, to afford pure brookite. The photocatalytic degradation of rhodamine B, tetramethylammonium chloride, and 4-chlorophenol on UV-illuminated pure brookite were investigated and compared with those on anatase and rutile TiO. The present research explores the generation of OH radicals as main oxidants on brookite. In addition, tetramethylammonium, as a mobile OH radical indicator, was degraded over both pure anatase and brookite phases, but not rutile. The brookite phase showed much higher photoactivity among TiO polymorphs, despite its smaller surface area compared with anatase. This result can be ascribed to the following properties of the brookite TiO film: (i) the higher driving force with more negative flat-band potential, (ii) the efficient charge transfer kinetics with low resistance, and (iii) the generation of more hydroxyl radicals, including mobile OH radicals. The brookite-nanostructured TiO electrode facilitates photocatalyst collection and recycling with excellent stability, and readily controls photocatalytic degradation rates with facile input of additional potential.