Facile synthesis of direct Z-scheme PPy/NH2-UiO-66 heterojunction for enhanced photocatalytic Cr(VI) reduction, industrial electroplating wastewater treatment, and tetracycline degradation

光催化 材料科学 异质结 化学工程 氧化还原 降级(电信) 光化学 化学 催化作用 光电子学 有机化学 计算机科学 电信 工程类 冶金
作者
Qi Wang,Shuzhen Zheng,Wanggang Ma,Jianying Qian,Lingye Huang,Hao Deng,Qi Zhou,Sirui Zheng,Shuangjun Li,Hao Du,Qiang Li,Derek Hao,Guoxiang Yang
出处
期刊:Applied Catalysis B-environmental [Elsevier]
卷期号:344: 123669-123669 被引量:60
标识
DOI:10.1016/j.apcatb.2023.123669
摘要

Z-scheme heterojunction photocatalysts generally have excellent redox ability and robust removal efficiency for contaminants in water. Herein, we combined p-type PPy and n-type NH2-UiO-66 by ball milling to prepare a direct Z-scheme PPy/NH2-UiO-66 photocatalyst with ultra-high redox potential. Notably, the optimized efficiency of PPy/NH2-UiO-66 (the mass ratio of PPy to NH2-UiO-66 is 1 wt%, named PPy/NU-1) rapidly reduced Cr(VI) (>95%, 60 min) and TC degradation (>90%, 180 min) at 100 W LED light. Moreover, the PPy/NU-1 has high stability and good anti-interference ability, which can effectively remove Cr(VI) from industrial electroplating wastewater, and the Cr(VI) removal rate is 99%, which meets the industrial wastewater standard and has the potential attraction of actual wastewater treatment. In addition, the techniques of UV-Vis diffuse reflection, electron spin resonance (ESR), photoluminescence (PL), and photoelectrochemical measurement showed that PPy/NH2-UiO-66 composites improved the light capture ability, thereby improving the photocatalytic efficiency. The PPy/NU-1 has a very high redox potential by constructing a Z-scheme heterojunction, enhances the interfacial charge transfer ability, and improves the separation efficiency of photogenerated carriers. Finally, the mechanism of the Z-scheme was systematically by nitroblue tetrazolium (NBT) and p-phthalic acid (TA) transformation, ESR experiments, and density functional theory (DFT) calculations. This work provides a strategy for the preparation of visible photocatalysts with excellent photocatalytic activity and provides new insights for interfacial charge transfer and molecular oxygen activation.
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