氧化还原
降级(电信)
激进的
盐(化学)
环境修复
化学
光化学
异质结
化学工程
核化学
材料科学
无机化学
催化作用
污染
有机化学
计算机科学
光电子学
工程类
生物
电信
生态学
作者
Gui Yang,Yujun Liang,Zhuoran Xiong,Jian Yang,Kun Wang,Zikang Zeng
标识
DOI:10.1016/j.cej.2021.130689
摘要
Photo-Fenton as an advanced oxidation technology has been proved as a multifunctional strategy for environmental remediation. In this study, a novel Ce4O7 modified Bi4MoO9 (C-BMO) Photo-Fenton heterojunction catalyst with the in-built dual redox centers (Ce4+/Ce3+ and Mo6+/Mo5+) was successfully constructed via a facile molten salt-assisted synthesis route. Systematic studies showed that 0.4C-BMO (0.4 meant the molar ratio of Ce and Bi was 0.4) heterojunction exhibited the optimal degradation rate of 2.16032 h−1 in the Photo-Fenton degradation of tetracycline (TC), being nearly 12.28 and 7.69 times higher than that of pristine Bi4MoO9 and Ce4O7. Such remarkably enhanced Photo-Fenton performance was mainly ascribed to the formation of intimate contacted interface favoring the highly effective transfer and spatial separation of photoexcited carriers, and the Ce4+/Ce3+ and Mo6+/Mo5+ cycling redox couples accelerating the activation of H2O2 to generate massive reaction radicals. Additionally, the possible Photo-Fenton degradation pathways of TC were proposed and the toxicity changes during TC degradation were detailed investigated. This present study broadens the application of Ce4O7 and highlights its promise in environmental remediation.
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