Manipulating the Fate of Charge Carriers with Tungsten Concentration: Enhancing Photoelectrochemical Water Oxidation of Bi2 WO6.

Bismuth tungstate (Bi2 WO6 ) thin film photoanode has exhibited an excellent photoelectrochemical (PEC) performance when the tungsten (W) concentration is increased during the fabrication. Plate-like Bi2 WO6 thin film with distinct particle sizes and surface area of different exposed facets are successfully prepared via hydrothermal reaction. The smaller particle size in conjunction with higher exposure extent of electron-dominated {010} crystal facet leads to a shorter electron transport pathway to the bulk surface, assuring a lower charge transfer resistance and thus minimal energy loss. In addition, it is proposed based on the results from conductive atomic force microscopy that higher W concentration plays a crucial role in facilitating the charge transport of the thin film. The "self-doped" of W in Bi2 WO6 will lead to the higher carrier density and improved conductivity. Thus, the variation in the W concentration during a synthesis can be served as a promising strategy for future W based photoanode design to achieve high photoactivity in water splitting application.

Pulsed Electrodeposition of Co3 O4 Nanocrystals on One-Dimensional ZnO Scaffolds for Enhanced Electrochemical Water Oxidation.

Pulsed electrodeposition has been introduced to deposit ultrathin flakes of Co3 O4 nanocrystals on ZnO nanorods. By fixing the seeding process, the scaffolding function of ZnO nanorods was studied by varying deposition times (30 s, 60 s, and 90 s) of Co3 O4 at a nucleation current of -1.0 mA cm-2 . The amount of deposited Co3 O4 has a strong influence on the oxygen evolution performance with ZnO scaffolds. To deliver a current density of 10.0 mA cm-2 in neutral solutions (0.5 M K2 SO4 ), the presence of ZnO scaffold electrodes negatively shifted the overpotential by ∼200 mV. In particular, the Co3 O4 /ZnO hybrid nanostructured electrode (60 s) exhibits the lowest onset potential of 1.5 V (vs. reversible hydrogen electrode, RHE). Electrochemical impedance spectra and double layer capacitance showed that the enhanced oxygen evolution activities originated from the improved charge transfer capability and the increased electrochemically active interface between Co3 O4 and ZnO.

Pulsed Electrodeposition of Co3 O4 Nanocrystals on One-Dimensional ZnO Scaffolds for Enhanced Electrochemical Water Oxidation.

Invited for this month's cover are the collaborative groups of Dr. Yun Hau Ng at University of New South Wales, Australia and Dr. Yiming Tang at South China Normal University, China. The front cover picture shows ultrathin Co3 O4 nanoflakes that are deposited on ZnO nanorods by pulsed electrodeposition. The performance of the nanostructured hybrid Co3 O4 /ZnO anode in electrochemical O2 evolution is better than that of neat Co3 O4 . Well-aligned one-dimensional ZnO nanorod arrays are integrated as a scaffold which functions as a "highway" to facilitate improved charge transfer, while the porosity of the anode material allows the penetration of the electrolyte, thus promoting efficient utilization of the catalytically active species. Read the full text of the article at 10.1002/cplu.201800218.

Oxygen-deficient bismuth tungstate and bismuth oxide composite photoanode with improved photostability.

A homogeneous layer of Bi2O3-Bi14WO24 composite (BWO/Bi2O3) thin film was fabricated using a combination of electrodeposition and thermal treatment. The evenly distributed Bi14WO24 component within the Bi2O3 layer was found to be important in stabilising the photoelectrochemical performances of Bi2O3 photoanode by promoting the photoelectron transport. The unmodified Bi2O3 suffered from severe photocorrosion as proven by X-ray diffraction (XRD) and inductively coupled plasma (ICP) analyses while the composite thin film was active without noticeable activity decay for at least 3 h of illumination. This strategy might be applicable to other photocatalysts with stability issues.