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TiO/WO 光阳极与 Sb-SnO 电极的协同催化作用,用于高效生成 ClO•,以处理尿液。

Synergistic catalysis of TiO/WO photoanode and Sb-SnO electrode with highly efficient ClO• generation for urine treatment.

机构信息

School of Environmental Science and Engineering, Key Laboratory of Thin Film and Microfabrication Technology (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, PR China.

School of Environmental Science and Engineering, Key Laboratory of Thin Film and Microfabrication Technology (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, PR China.

出版信息

J Hazard Mater. 2024 May 15;470:134118. doi: 10.1016/j.jhazmat.2024.134118. Epub 2024 Mar 24.

Abstract

Urine is the major source of nitrogen pollutants in domestic sewage and is a neglected source of H. Although ClO• is used to overcome the poor selectivity and slow kinetics of urea decomposition, the generation of ClO• suffers from the inefficient formation reaction of HO• and reactive chlorine species (RCS). In this study, a synergistic catalytic method based on TiO/WO photoanode and Sb-SnO electrode efficiently producing ClO• is proposed for urine treatment. The critical design is that TiO/WO photoanode and Sb-SnO electrode that generate HO• and RCS, respectively, are assembled in a confined space through face-to-face (TiO/WO//Sb-SnO), which effectively strengthens the direct reaction of HO• and RCS. Furthermore, a Si solar panel as rear photovoltaic cell (Si PVC) is placed behind TiO/WO//Sb-SnO to fully use sunlight and provide the driving force of charge separation. The composite photoanode (TiO/WO//Sb-SnO @Si PVC) has a ClO• generation rate of 260% compared with the back-to-bake assembly way. In addition, the electrons transfer to the NiFe LDH@Cu NWs/CF cathode for rapid H production by the constructed photoelectric catalytic (PEC) cell without applied external biasing potential, in which the H production yield reaches 84.55 μmol h with 25% improvement of the urine denitrification rate. The superior performance and long-term stability of PEC cell provide an effective and promising method for denitrification and H generation.

摘要

尿液是生活污水中氮污染物的主要来源,也是被忽视的 H 产生源。尽管 ClO•可用于克服尿素分解的选择性差和动力学缓慢的问题,但 ClO•的生成受到 HO•和活性氯物质(RCS)的形成反应效率低的限制。在这项研究中,提出了一种基于 TiO/WO 光阳极和 Sb-SnO 电极的协同催化方法,可有效产生 ClO•,用于尿液处理。关键设计是,分别生成 HO•和 RCS 的 TiO/WO 光阳极和 Sb-SnO 电极通过面对面(TiO/WO//Sb-SnO)组装在一个受限空间内,这有效地增强了 HO•和 RCS 的直接反应。此外,将 Si 太阳能电池板作为背面光伏电池(Si PVC)放置在 TiO/WO//Sb-SnO 后面,以充分利用阳光并提供电荷分离的驱动力。与背面烘烤组装方式相比,复合光阳极(TiO/WO//Sb-SnO@Si PVC)的 ClO•生成速率提高了 260%。此外,通过构建的光电催化(PEC)电池,电子转移到 NiFe LDH@Cu NWs/CF 阴极,用于快速 H 生产,无需施加外部偏置电势,其中 H 产量达到 84.55 μmol h,尿液脱硝率提高了 25%。PEC 电池的优异性能和长期稳定性为脱硝和 H 生成提供了一种有效且有前景的方法。

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