Abstract
Unusually high photocatalytic activity of visible light-induced O₂ generation can be achieved by electrostatically-derived self-assembly between exfoliated Zn-Cr-LDH 2D nanosheets and POM 0D nanoclusters (W₇O₂₄⁶⁻ and V₁₀O₂₈⁶⁻) acting as an electron acceptor. This self-assembly can provide a high flexibility in the control of the chemical composition and pore structure of the resulting LDH-based nanohybrids. The hybridization with POM nanoclusters remarkably enhances the photocatalytic activity of the pristine Zn-Cr-LDH, which is attributable to the formation of porous structure and depression of charge recombination. Of prime interest is that the excellent photocatalytic activity of the as-prepared Zn-Cr-LDH-POM nanohybrid for visible light-induced O₂ generation can be further enhanced by calcination at 200 °C, leading to the very high apparent quantum yield of ∼75.2% at 420 nm. The present findings clearly demonstrate that the self-assembly of LDH-POM is fairly powerful in synthesizing novel LDH-based porous nanohybrid photocatalyst for visible light-induced O₂ generation.