具有共轭 S 型电荷调动功能的 MOF 衍生分层 α-Bi2O3-BiVO4-CuFe2O4 多结异质结构:光催化去污研究、毒性评估和机理阐明

Swagat Kumar Nayak, Sibun Kumar Pradhan, Saumyaranjan Panda, Ranjit Bariki, B.G. Mishra
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摘要

通过将一键式 MOF 衍生的 BiO-BiVO 微晶块与铜氧化铁纳米片整合在一起,设计出了一系列分层的 α-BiO-BiVO-CuFeO 多结异质结构。通过 MOF 衍生途径,BiO-BiVO 获得了相互连接的多孔结构。综合研究表明,该材料保留了结晶相,具有最佳的光收集能力、更长的使用寿命、较大的电化学活性表面积和更好的电荷动力学特性。这种异质结构能有效地光降解具有潜在毒性和致突变性的间苯三酚(MTE)除草剂,降解率是母体半导体的 6-12 倍。根据 QSAR 方案分析,光降解的最终产物在急性毒性、生物累积因子和致突变性方面均大大低于母体 MTE。在 60 分钟的照射时间内,异质结构对细菌的完全光灭活同样有效。扫描电子显微镜(SEM)、原子力显微镜(AFM)高度剖面和共聚焦显微镜研究提供了有关光灭活过程的重要信息。根据详细的能带结构分析,提出了共轭 S 型电子传递机制,从而阐明了多接面光催化剂活性的提高。
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MOF derived hierarchical α-Bi2O3-BiVO4-CuFe2O4 multijunction heterostructure with conjugated S-scheme charge mobilization: Photocatalytic decontamination study, toxicity assessment and mechanistic elucidation
A series of hierarchical α-BiO-BiVO-CuFeO multijunction heterostructure was designed by integrating one-pot MOF derived BiO-BiVO microrods with CuFeO nanosheets. The MOF-derived route afforded BiO-BiVO with interconnecting porous architecture. Comprehensive investigations revealed preservation of crystalline phases, optimal light harvesting ability, higher lifetime, large electrochemically active surface area and improved charge dynamics. The heterostructure efficiently performed the photo-degradation of potentially toxic and mutagenic mesotrione (MTE) herbicide with rates 6–12 times greater than the parent semiconductors. The photo-degraded end products displayed profoundly less acute toxicity, bioaccumulation factor and mutagenic nature than parent MTE as analyzed by QSAR protocol. The heterostructure was equally effective for complete photo-inactivation of bacteria within 60 min of irradiation. SEM, AFM height profile and confocal microscopic investigation provided crucial information about the photo-inactivation process. A conjugated S-scheme electron transfer mechanism was proposed based on detailed band structure analysis to elucidate the improved activity of the multijunction photocatalyst.
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