Developing noble metal-free water oxidation catalysts is essential for many energy conversion/storage processes (e.g., water splitting). Herein, we report the facile synthesis of hollow Co3O4 microspheres composed of porous, ultrathin (<5 nm), single-crystal-like nanosheets via a novel "self-template" route. The successful preparation of these hollow Co3O4 nanomaterials includes three main steps: (1) the synthesis of solid cobalt alkoxide microspheres, (2) their subsequent self-template conversion into hollow cobalt hydroxide microspheres composed of ultrathin nanosheets, and finally (3) thermal treatment of hollow cobalt hydroxide microspheres into the hollow Co3O4 material. The as-obtained hollow Co3O4 nanomaterial possesses a high BET surface area (∼180 m(2) g(-1)), and can serve as an active and stable water oxidation catalyst under both electrochemical and photochemical reaction conditions, owing to its unique structural features. In the electrochemical water oxidation, this catalyst affords a current density of 10 mA cm(-2) (a value related to practical relevance) at an overpotential of ∼0.40 V. Moreover, with the assistance of a sensitizer [Ru(bpy)3](2+) (bpy = 2,2'-bipyridine), this nanomaterial can catalyze water oxidation reactions under visible light irradiation with an O2 evolution rate of ∼12 218 μmol g(-1) h(-1). Our results suggest that delicate nanostructuring can offer unique advantages for developing efficient water oxidation catalysts.

We present a facile synthetic method that yields Ag@Co x P core–shell-type heterogeneous nanostructures with excellent oxygen evolution reaction (OER) activity. This nanocatalyst can deliver a current density of 10 mA/cm2 at a small overpotential of 310 mV and exhibits high catalytic stability. Additionally, the catalytic activity of Ag@Co x P is 8 times higher than that of the Co2P nanoparticles, owing primarily to the strong electronic interaction between the Ag core and the Co x P shell.

It is highly desirable to develop durable photocatalysts for efficiently boosting water splitting, but it is challenging for CdS to realize the expected result without using any hole sacrificial agents. Herein, improved photocatalytic hydrogen evolution and enhanced stability are simultaneously realized in the absence of any sacrificial agents by introducing Zinc 5-, 10-, 15-, 20-mesotetra (4-hydrazidephenyl) porphyrin (ZnTHPP) onto CdS nanosheets (CdS NSs). In this system (ZnTHPP/CdS NSs), a novel hole transfer channel is achieved by an internal chemical reaction using the functional group of acylhydrazine in ZnTHPP. Compared with CdS NSs, the ZnTHPP/CdS NSs exhibit excellent photostability (15 h) and efficient photocatalytic activity for pure water splitting (≈6.4 times). Furthermore, it is found that the rate constant for photogenerated holes is about 1.7 times higher than the pure CdS NSs under light irradiation. This suggests that the promising charge transfer channel can efficiently suppress charge recombination and photocorrosion of pure CdS NSs. The pattern via internal charge transfer channel not only can solve the stability of CdS based materials, but also design more semiconductors for efficient photocatalytic water splitting.

A boronized nickel plate shows surface structural evolution and activity enhancement during the OER due to synergistic geometric and electronic effects, and shows good catalytic stability for over 1500 hours.

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Despite the superior oxygen evolution electrocatalytic activity of metal-selenide nanostructures, especially when compared with their oxide counterparts, the origin behind their excellent activity remains unclear.

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