Search

As a visible-light response semiconductor materials, bismuth vanadate (BiVO4) is extensively applied in photodegradation organic dye field. In this study, we synthesized C3N5 nanosheets and coupled with decahedral BiVO4 to construct a Z-scheme C3N5/BiVO4 heterostructure with close interface contact. By introducing C3N5 into BiVO4, the built Z-scheme transfer pathway provides silky channel for charge carrier migration between different moieties and enables photoexcited electrons and holes accumulated on the surface of BiVO4 and C3N5. The accelerated separation of charge carriers ensures C3N5/BiVO4 heterostructures with a powerful oxidation capacity compared with pure BiVO4. Due to the synergistic effect in Z-scheme heterostructure, the C3N5/BiVO4 demonstrated an improved photodegradation ability of rhodamine B (RhB) and methylene blue (MB) that of bare BiVO4. [ABSTRACT FROM AUTHOR]

Introducing piezoelectric materials with the built-in electric field caused by mechanical force has been confirmed as an effective strategy to boost the separation efficiency of photoexcited charge carriers that determines the photocatalytic performance. In this study, we introduced Bi4Ti3O12 with superior piezoelectric properties into BiVO4–Bi4V2O10 materials to synthesize a 2D Bi4Ti3O12–BiVO4–Bi4V2O10 photocatalyst via a facile hydrothermal method. Compared with bare BiVO4, the Bi4Ti3O12–BiVO4–Bi4V2O10 piezo-photocatalytic activity towards Cr(VI) removal and oxygen evolution is boosted remarkably under both illumination and ultrasound treatments. The promoted photocatalytic activity can be ascribed to the accelerated photoexcited carrier separation efficiency driven by the polarization electric field and the synergy effect in the heterostructure. This work provides a simple and sustainable strategy for the design and development of piezo-photocatalysts with high photoredox activity capacity. [ABSTRACT FROM AUTHOR]

The construction of Z-scheme heterostructures using matching band semiconductors is an effective strategy for producing highly efficient photocatalysts. In this study, MgIn 2 S 4 (MIS) was grown in situ on In 2 O 3 microrods created with an In-based MOF material (In-MIL-68) as a template to successfully establish a unique MIS-In 2 O 3 heterojunction with a well-matched Z-scheme interface charge transfer channel. Tetracycline (TC) as a typical antibiotic was chosen as the target pollutant to evaluate the photocatalytic activity. After 120 min of visible light irradiation, the MIS-In 2 O 3 -(10:1) material had the greatest photocatalytic degradation activity of tetracycline with 96.55%, which was 2.39 and 4.26 times that of MIS and In 2 O 3 , respectively. The improved photocatalytic activity is attributed to the in situ growth of MIS on In 2 O 3 , forming a Z-scheme heterojunction at the interface, which not only increases the specific surface area, exposes the abundant active site, and improves light utilization but also facilitates the migration and separation of photogenic carriers. The photocatalytic degradation products of TC were detected by liquid chromatography-mass spectrometry (LC-MS), and a preliminary degradation pathway was proposed. Radical capture experiments and ESR analysis confirmed that the main active species were holes (h + ), superoxide radicals ( • O 2 - ), and superoxide and hydroxyl radicals ( • OH). Finally, combined with band position analysis, this study proposes a direct Z-scheme heterojunction mechanism to improve the photocatalytic degradation of tetracycline in MIS under visible light.

Introducing piezoelectric materials with the built-in electric field caused by mechanical force has been confirmed as an effective strategy to boost the separation efficiency of photoexcited charge carriers that determines the photocatalytic performance. In this study, we introduced Bi 4 Ti 3 O 12 with superior piezoelectric properties into BiVO 4 -Bi 4 V 2 O 10 materials to synthesize a 2D Bi 4 Ti 3 O 12 -BiVO 4 -Bi 4 V 2 O 10 photocatalyst via a facile hydrothermal method. Compared with bare BiVO 4 , the Bi 4 Ti 3 O 12 -BiVO 4 -Bi 4 V 2 O 10 piezo-photocatalytic activity towards Cr(VI) removal and oxygen evolution is boosted remarkably under both illumination and ultrasound treatments. The promoted photocatalytic activity can be ascribed to the accelerated photoexcited carrier separation efficiency driven by the polarization electric field and the synergy effect in the heterostructure. This work provides a simple and sustainable strategy for the design and development of piezo-photocatalysts with high photoredox activity capacity.

Bismuth vanadate (BiVO 4 ) is a promising photocatalyst for water pollution degradation and photocatalytic oxygen evolution. In this work, we prepared 2D/2D BiVO 4 -Bi 4 V 2 O 10 heterostructure with tight interfacial contact via a facile one-step hydrothermal process. The crystal structure and morphology of the samples could be easily regulated by changing the pH values of the solution. The BiVO 4 -Bi 4 V 2 O 10 heterostructure exhibited an enhanced photodegradation rate of Cr(VI) and oxygen evolution that of bare BiVO 4 , indicating that the synergistic effect and the interfacial fusions between BiVO 4 and Bi 4 V 2 O 10 can effectively promote the migration and separation rate of photoexcited charge carriers.