Abstract

Accelerating the separation efficiency of photoexcited electron-hole pairs with the help of binary heterojunction structure is considered to be a promising approach for significantly enhancing the photocatalytic hydrogen production performance of TiO2. Providing more (Sr0.6Bi0.305)2Bi2O7 (SBO) catalysts to function as active sites of TiO2, together with the ability to construct heterojunction structures, is highly desirable for photocatalytic hydrogen evolution and pollutant photodegradation. To achieve this goal, in this work, (Sr0.6Bi0.305)2Bi2O7/P25 (SBO/P25) binary heterojunction catalyst is formed in situ on the TiO2 surface by a simple one-step hydrothermal method. To evaluate the feasibility of SBO/P25 as a very efficient photocatalyst for degradation of MB and photocatalytic hydrogen evolution, a series of photocatalytic experimental studies were carried out. The experimental result indicated that the existence of heterojunction structure in the SBO/P25 nanocomposites improves the photocatalytic activity of P25. The photocatalytic performance of H2 evolution from water splitting and MB degradation for an optimal SBO/P25 photocatalyst reached 3.18 mmol g–1 h−1 and 3.42 × 10−2 min−1, respectively, which were 7.40 and 5.26 times higher than those of pure P25, respectively. The significantly improved catalytic capability on SBO/P25 is mainly ascribed to the enhanced visible light absorption and charge transfer in comparison with P25. In addition, SBO/P25 composites have excellent stability and recyclability, showing great potential for application in wastewater treatment and photocatalytic hydrogen evolution.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.