Article ID Journal Published Year Pages File Type
6453666 Applied Catalysis B: Environmental 2018 11 Pages PDF
Abstract

•Plate-like BiOCl/2D networks Bi2S3 heterostructures were synthesized.•The selective ion-exchange reaction was observed in the growth process.•The crystal lattice matching are responsible for the topotactic transformation.•The BiOCl/Bi2S3 exhibited enhanced photocatalytic activity.

We herein demonstrate the uniform porous hierarchical plate-like BiOCl/2D networks Bi2S3 heterostructures realized by a facile two-step hydrothermal technique. The synthesis involved an anion exchange process by reacting pre-synthesized BiOCl irregular octagonal nanoplates with Na2S2O3·5H2O in an aqueous solution. The experiment results revealed that the 3D plate-like heterostructures were composed of internal BiOCl and outside networks interwoven by 1D Bi2S3 nanorods. Interestingly, the heterostructures had almost the same thickness and the bigger length compared to the precursor BiOCl. We proposed the possible formation mechanism of the composites which involved selective ion-exchange reaction, the following Ostwald ripening process and epitaxial growth. And the crystal lattice matching between the a- or b-axis of tetragonal BiOCl (a = b = 3.89 Å) and the a-axis of orthorhombic Bi2S3 (a = 3.981 Å) could be responsible for the in-situ topotactic transformation. Due to the formation of hetero-nanostructures, the unique spatial architecture features and the existence of oxygen vacancies, the BiOCl/Bi2S3 composites exhibited significantly extended photo-responsive range and improved photocatalytic activity for reduction of CrVI under visible-light irradiation. Moreover, the possible mechanism of photocatalysis process was investigated. Our work is expected to inspire further attempts for hierarchical and unconventional hetero-nanostructures with unique spatial architecture, which is very promising for photocatalysis and other applications.

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Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
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