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Highly Efficient Visible Light-Induced O2 Generation by Self-Assembled Nanohybrids of Inorganic Nanosheets and Polyoxometalate Nanoclusters

机译:无机纳米片和多金属氧酸盐纳米团簇的自组装纳米杂化物高效产生可见光诱导的O2

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摘要

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.
机译:可通过剥落的Zn-Cr-LDH 2D纳米片和POM 0D纳米团簇(W7O24 6-和V10O28 )之间的静电自组装来实现可见光诱导的O2异常高的光催化活性6 − )充当电子受体。这种自组装可以在控制所得的基于LDH的纳米杂化物的化学组成和孔结构方面提供高度的灵活性。与POM纳米簇的杂交显着增强了原始Zn-Cr-LDH的光催化活性,这归因于多孔结构的形成和电荷重组的降低。最令人感兴趣的是,通过在200°C下煅烧,可以进一步增强所制备的Zn-Cr-LDH-POM纳米杂化物对可见光诱导的O2生成的优异的光催化活性,从而导致〜的非常高的表观量子产率。在420nm处为75.2%。目前的发现清楚地表明,LDH-POM的自组装在合成新型的基于LDH的多孔纳米杂化光催化剂中,对于可见光诱导的O2生成是相当强大的。

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