Abstract

Photocatalytic performance of semiconductors is currently limited by low solar light utilization, rapid charge recombination and limited reactive sites. Reducing the thickness of layered photocatalysts can shorten the charge transport distance to inhibit their recombination and provide more reactive sites. Surface ionic grafting can broaden the light absorption range and promote the separation efficiency of carriers. In this work, the surface iodine ion modified Bi2O2[BO2(OH)] nanosheets are synthesized by combining the surfactant-assisted hydrothermal method and room-temperature KI solution treatment route. These nanosheets show increased photoabsorption in visible region, enlarged specific surface area and promoted charge separation. Compared with the pristine Bi2O2[BO2(OH)], the surface I- modified Bi2O2[BO2(OH)] nanosheets exhibit substantially strengthened photocatalytic performance for degradation of BPA, which increases beyond 25 times. The total organic carbon content (TOC) test reveals that the mineralization process of BPA. Electron spin resonance (ESR) measurements disclose the radicals that play dominant role in the photocatalytic process and confirm their increased yield over I- modified Bi2O2[BO2(OH)] nanosheets. In addition, BiOB-S-I2 also shows universality for degradation of a variety of high-concentration pollutants, including rhodamine B, methyl orange, methylene blue, phenol, 2,4-dichlorophenol and tetracycline hydrochloride. This study may provide a combined strategy for exploring high-performance photocatalysts via microstructure control and surface ionic decoration.

Full Text
Paper version not known

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.