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可见光光催化燃料电池中同时 PMS 激活增强的非诺贝特降解和发电。

Enhanced bezafibrate degradation and power generation via the simultaneous PMS activation in visible light photocatalytic fuel cell.

机构信息

Key Laboratory of the Three Gorges Reservoir Regions Eco-Environment, Ministry of Education, Chongqing University, Chongqing 400045, China.

Key Laboratory of the Three Gorges Reservoir Regions Eco-Environment, Ministry of Education, Chongqing University, Chongqing 400045, China.

出版信息

Water Res. 2021 Dec 1;207:117800. doi: 10.1016/j.watres.2021.117800. Epub 2021 Oct 25.

Abstract

A collaborative system including peroxymonosulfate (PMS) activation in a photocatalytic fuel cell (PFC) with an BiOI/TiO nanotube arrays p-n type heterojunction as photoanode under visible light (PFC(BiOI/TNA)/PMS/vis system) was established. Xenon lamp was used as the light source of visible light. A 4.6 times higher pseudo-first-order bezafibrate (BZF) degradation rate constant was achieved in this system compared with the single PFC(BiOI/TNA)/vis system. The radical quenching experiments revealed that the contribution of reactive oxidative species (ROS) followed the order of O ≈ h >> •OH > SO >>O. The EPR tests demonstrated that PMS addition enlarged the formation of O, •OH and SO, but suppressed O yield. Interestingly, O was further proved to dominantly originated from the priority reaction between positive photoinduced holes (h) and negatively charged PMS. Besides, N-purging tests and density functional theory calculation indicated that PMS probably reacted with residual photoinduced electron (e) on the more negative conduction band (CB) of BiOI to form •OH and SO, but competed with dissolved oxygen. Other e transferred to the less negative CB of TNA through p-n junction will efficiently move to cathode through the external circuit. The greatly promoted power generation of PFC system was observed after PMS addition due to extra h consumption and efficient e separation and transfer. Besides, three possible pathways for BZF degradation were proposed including hydroxylation, fibrate chain substituent and amino bond fracture. This study can provide new insights into the mechanisms of PMS assisted photocatalysis and accompanying energy recovery.

摘要

建立了一种协同体系,包括在可见光下用光阳极 BiOI/TiO 纳米管阵列 p-n 型异质结(PFC(BiOI/TNA))中激活过一硫酸盐(PMS)的光催化燃料电池(PFC)(PFC(BiOI/TNA)/PMS/vis 系统)。氙灯用作可见光光源。与单一 PFC(BiOI/TNA)/vis 系统相比,该系统中假一级贝扎贝特(BZF)的降解速率常数提高了 4.6 倍。自由基猝灭实验表明,活性氧化物种(ROS)的贡献顺序为 O ≈ h >> •OH > SO >>O。EPR 测试表明,添加 PMS 会增加 O、•OH 和 SO 的形成,但会抑制 O 的生成。有趣的是,进一步证明 O 主要源自正光生空穴(h)和带负电荷的 PMS 之间的优先反应。此外,N 吹扫测试和密度泛函理论计算表明,PMS 可能与 BiOI 更负的导带(CB)上的残留光致电子(e)反应形成•OH 和 SO,但与溶解氧竞争。其他通过 p-n 结转移到 TNA 较负的 CB 的 e 通过外部电路有效地转移到阴极。由于额外的 h 消耗以及有效的 e 分离和转移,添加 PMS 后,PFC 系统的发电得到了极大的促进。此外,还提出了 BZF 降解的三种可能途径,包括羟化、纤维酸链取代和氨基键断裂。这项研究可为 PMS 辅助光催化及其伴随的能量回收机制提供新的见解。

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