Highly Efficient Visible Light-Induced O2 Generation by Self-Assembled Nanohybrids of Inorganic Nanosheets and Polyoxometalate Nanoclusters
nanotechnology
transmission electron microscopy
powder diffraction
02 engineering and technology
0210 nano-technology
7. Clean energy
Article
inorganic compound
DOI:
10.1038/srep02080
Publication Date:
2013-06-26T09:03:33Z
AUTHORS (5)
ABSTRACT
Unusually high photocatalytic activity of visible light-induced O(2) generation can be achieved by electrostatically-derived self-assembly between exfoliated Zn-Cr-LDH 2D nanosheets and POM 0D nanoclusters (W(7)O(24)(6−) and V(10)O(28)(6−)) 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 O(2) 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 O(2) generation.
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