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Published on: August 23, 2012
Construction of visible light driven silver sulfide/graphitic carbon nitride p-n heterojunction for improving
Weiyuan Zuo1, Ling Liang2, Fanggui Ye2
1State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources, College of Chemistry and Pharmaceutical Science of Guangxi Normal University, Guilin, 541004, PR China; Key Laboratory of Regional Ecological Environment Analysis and Pollution Control of West Guangxi, College of Chemistry and Environmental Engineering, Baise University, Baise, 533000, PR China.
Abstract:
Compared with the Z-scheme and type-II heterojunctions, p-n type heterojunctions are more favorable for the migration of photo-induced carriers owing to the advantage of built-in electric fields. In addition, it is still of great significance to understand the carrier migration properties of the p-n heterojunction. Therefore, the development of new p-n heterojunctions and the development of high-efficiency catalysts with effective modulation of light responsiveness and rapid transfer of charge to achieve photocatalytic inactivation have attracted much attention. In this study, we synthesized a Ag2S/g-C3N4 heterojunction via the in situ deposition of Ag2S onto the g-C3N4 substrate. The prepared Ag2S/g-C3N4 composite facilitated photo-generated charge carrier transfer and exhibited outstanding photocatalytic inactivation of bacteria compared to that of a single catalyst under visible light irradiation. In addition, the ACN-2 composites fully deactivated 7 log10 CFU/mL E. coli and 7 log10 CFU/mL S. aureus cells in 90 min under visible light. The quenching experiments confirmed that photo-generated active species (O2-, OH, and h+) were the major reactive oxygen species that contributed to the inactivation of bacteria. Energy band alignment analysis indicated that a type-II band alignment was formed in the p-n heterostructure, thereby providing strong support for the photocatalytic mechanism. This study not only provides insights into the design of p-n heterostructures, but also presents a promising strategy to enhance the photocatalytic capacities of g-C3N4 based materials for pathogen inactivation.

