BiVO4 quadrangular nanoprisms with highly exposed {101} facets for selective photocatalytic oxidation of benzylamine
Photocatalytic oxidation of amines to high value-added imines is crucial but challenging. The adsorption ability to reactant molecules and the charge separation ability are important factors affecting the reactivity. Different facets of monoclinic BiVO4 (m-BiVO4) have varied electronic structures, l...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2022-09, Vol.10 (37), p.19699-19709 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Photocatalytic oxidation of amines to high value-added imines is crucial but challenging. The adsorption ability to reactant molecules and the charge separation ability are important factors affecting the reactivity. Different facets of monoclinic BiVO4 (m-BiVO4) have varied electronic structures, leading to differences in the adsorption ability and charge separation ability. Thus, tailoring the exposed facets is a promising strategy to optimize the reactivity. Herein, the density functional theory (DFT) calculations demonstrate that for m-BiVO4, both the benzylamine (BnNH2) adsorption ability and charge separation ability of {101} facets were stronger than those of {110} facets. These results motivate us to synthesize m-BiVO4 quadrangular nanoprisms (Q-BiVO4) with highly exposed {101} facets through a colloidal two-phase method. Q-BiVO4 exhibits highly enhanced charge separation efficiency and excellent photocatalytic performance for oxidizing BnNH2 to N-benzylidenebenzylamine (N-BB). More impressively, the efficient charge transfer between Q-BiVO4 and BnNH2 was directly confirmed via single-particle spectroscopy in situ. This work provides direct evidence to deeply understand the interaction between Q-BiVO4 and the reactant molecules and provides insights for rational design of photocatalysts with specific exposed facets for selective oxidation of amines. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d2ta01758j |