Murad Z. A. Warshagha, Ziyaur Rasool, Mohammad Saud Athar, Mohammad Muneer, Hatem M. Altass, Raad Felemban, Abdelrahman S. Khder and Saleh A. Ahmed
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The AgBr–NiO composite showed greater photocatalytic degradation efficiency than bare AgBr and NiO when exposed to visible light for the colored anionic dye rhodamine B (RhB) and bisphenol A (BPA), a colorless endocrine-disrupting contaminant (EDC), resulting in high photocatalytic activity for the degradation of RhB (97.6% in 11 min) and BPA (85% in 120 min). Additionally, a notable decrease in TOC over time was observed under similar reaction conditions in the photo-mineralization examination of both model pollutants. Trapping tests were conducted to determine which reactive oxygen species (ROS) were involved in the degradation process. A plausible Z-scheme mechanism for this n–p heterojunction was proposed to explain the formation of e<small><sup>−</sup></small>/h<small><sup>+</sup></small> pairs induced by visible light. 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引用次数: 0
摘要
采用一锅溶胶-凝胶法制备了一种高效、独特的AgBr-NiO二元异质结。利用x射线衍射(XRD)、扫描电子显微镜(SEM)、能量色散x射线(EDX)分析、透射电子显微镜(TEM)、布鲁诺尔-埃米特-泰勒(BET)、紫外-可见漫反射光谱(UV-vis-DRS)、傅里叶变换红外光谱(FTIR)和光致发光(PL)等分析技术仔细检查了所制备材料的物理化学性质。BET分析显示AgBr-NiO具有介孔性质和高表面性能。在可见光下,AgBr-NiO复合材料对有色阴离子染料罗丹明B (RhB)和无色内分泌干扰污染物双酚A (BPA)的光催化降解效率高于裸AgBr和NiO,对RhB和BPA的光催化降解活性分别为11 min 97.6%和120 min 85%。此外,在两种模式污染物的光矿化检测中,在相似的反应条件下,TOC随时间的显著降低。进行了捕集试验以确定哪些活性氧(ROS)参与了降解过程。提出了一种合理的n-p异质结的z图式机制来解释可见光诱导下e-/h+对的形成。本研究有助于开发具有高生物活性和低毒性的可回收光催化剂。
Development of a crystalline n-AgBr/p-NiO binary heterojunction for photocatalytic degradation of organic contaminants with accompanying mineralization, adsorption, and antimicrobial studies†
A highly effective and unique AgBr–NiO binary heterojunction was developed using an effective one-pot sol–gel method. The physicochemical properties of the produced materials were carefully examined using analytical techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX) analysis, transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET), ultraviolet-visible diffuse reflectance spectroscopy (UV-vis-DRS), Fourier transform infrared spectroscopy (FTIR), and photoluminescence (PL). The mesoporous nature and high surface properties of AgBr–NiO were revealed by the BET analysis. The AgBr–NiO composite showed greater photocatalytic degradation efficiency than bare AgBr and NiO when exposed to visible light for the colored anionic dye rhodamine B (RhB) and bisphenol A (BPA), a colorless endocrine-disrupting contaminant (EDC), resulting in high photocatalytic activity for the degradation of RhB (97.6% in 11 min) and BPA (85% in 120 min). Additionally, a notable decrease in TOC over time was observed under similar reaction conditions in the photo-mineralization examination of both model pollutants. Trapping tests were conducted to determine which reactive oxygen species (ROS) were involved in the degradation process. A plausible Z-scheme mechanism for this n–p heterojunction was proposed to explain the formation of e−/h+ pairs induced by visible light. The proposed work facilitates the development of a recyclable photocatalyst characterized by high biological activity and low toxicity.