Heterostructure engineering of resorcinol-formaldehyde resins and sulfur-vacancy-containing Zn3In2S6 for high-efficiency photocatalytic H2O2 production

Abstract

Resorcinol-formaldehyde (RF) resins have garnered significant interest due to their remarkable efficiency in producing photocatalytic H2O2. The combination of RF with inorganic semiconductors to create organic–inorganic heterojunctions represents a promising strategy for enhancing photocatalytic activity. In this work, RF was coated onto Zn3In2S6 nanoflowers with sulfur-vacancy, creating RF/Zn3In2S6 composites with an S-scheme heterostructure. This novel composite exhibited superior photocatalytic activity for H2O2 production in both pure water and seawater, without sacrificial agents. Specifically, the production rate of RF/Zn3In2S6-0.3 in pure water under simulated solar illumination achieved 3174.34 μmol/h/g, marking 8.53 and 4.17 times over RF and Zn3In2S6, respectively. Moreover, its photocatalytic activity in seawater reached an impressive 2290.81 μmol/h/g, 4.93 and 3.12 times greater than that of RF and Zn3In2S6, respectively. The enhanced photocatalytic activity is attributed to the S-scheme charge transfer mechanism, which facilitates efficient charge separation and amplifies redox capabilities. Both experimental and density function theory analyses confirm the S-scheme route in RF/Zn3In2S6-0.3 for photocatalytic H2O2 production. This study not only presents the first account of an organic semiconductor RF being employed in an S-scheme heterojunction interface but also introduces the surface sulfur-vacancy mediated S-scheme heterojunction strategy for photocatalytic H2O2 production, representing a significant advancement in the field.