Synergistic effect of novel pyrite/N-doped reduced graphene oxide composite with heterojunction structure for enhanced photo-assisted reduction of Cr(VI) in oxic water: Specific role of molecular oxygen

• Published in: The Science of the total environment 2024-01, Vol.907, p.168123-168123, Article 168123
• Main Authors: Yang, Kunlun, Chi, Yanxiao, Yang, Yuxuan, Lou, Zimo, Wang, Tonghui, Wang, Dengyang, Miao, Hengfeng, Xu, Xinhua
• Format: Article
• Language: English
• Subjects: aerobic conditions; catalysts; chromium; decontamination; dissolved oxygen; electron paramagnetic resonance spectroscopy; graphene; graphene oxide; Hexavalent chromium; irradiation; Oxic water; oxygen; Photo-assisted reduction; photocatalysis; pyrite; Pyrite/N-doped reduced graphene oxide composite; species; synergism; Type II heterojunction
• ISSN: 0048-9697; 1879-1026
• DOI: 10.1016/j.scitotenv.2023.168123

To avoid severe aggregation and synergistically utilize the intrinsic and photocatalytic reducibility, pyrite (FeS2) was loaded onto N-doped reduced graphene oxides (N-rGO) to fabricate a novel FeS2/N-rGO heterojunction catalyst for enhanced chromium (Cr(VI)) reduction in oxic condition to simultaneously investigate the specific effect and role of dissolved oxygen (DO). Characterization results showed that strong interaction and combination of FeS2 and N-rGO not only achieved the uniform distribution of FeS2, but also increased the defects, and exposed more functional groups. Meanwhile, the Type II heterojunction was formed in FeS2/N-rGO, which facilitated the separation efficiency of photo-generated carriers and electrons, endowing FeS2/N-rGO a superior photocatalytic activity. Cr(VI) was almost completely reduced via FeS2/N-rGO within 60 min under irradiation (Cr(VI) = 10 mg/L, dosage = 0.2 g/L), 3 times that of pristine FeS2 (18.7 %). Trapping and Electron Spin Resonance (ESR) experiments indicated that photo-generated e− and derived O2− species from photoactivation of dioxygen (DO) were the key reactive species for the enhancement of photo-assisted Cr(VI) reduction, rather than reductive Fe2+ and S22− species. Although the photocatalysis of FeS2/N-rGO cannot directly generate hydroxyl radicals (OH), the oxidative OH ascribed to superoxide radicals (O2−), photo-induced holes and free DO preferentially consumed by Fe2+ and S22− with stronger reducibility. Hence, as compared to the anoxic condition, the reduction rate of Cr(VI) was slightly decreased, but still can be totally removed within 60 min in the oxic conditions. Due to the excessive amount of FeS2/N-rGO, Cr(III) after reduction would not be influenced by oxidative species and maintain stability under oxic condition. This study provided a facile modification strategy for FeS2 based composites and uncovered its working mechanism for Cr(VI) decontamination. [Display omitted] •Type II heterojunction was constructed to improve photocatalysis activity of FeS2/N-rGO.•More defects and functional reductive active sites (Fe2+ and S22−) were generated and exposed on FeS2/N-rGO.•Photo-generated e− and derived O2− were key reactive species for enhancement of photo-assisted Cr(VI) reduction.•Photo-induced h+, oxidative OH and DO in oxic water were preferentially consumed by Fe2+ and S22−.