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通过在一体化NiFeO/g-CN复合纳米颗粒之间插入零维电子介质将II型异质结转变为Z型异质结:促进光芬顿降解的自由基生成

Conversion of a Type-II to a Z-Scheme Heterojunction by Intercalation of a 0D Electron Mediator between the Integrative NiFeO/g-CN Composite Nanoparticles: Boosting the Radical Production for Photo-Fenton Degradation.

作者信息

Palanivel Baskaran, Mani Alagiri

机构信息

Department of Physics and Nanotechnology, SRM Institute of Science and Technology, Kattankulathur, Kancheepuram 603203, Tamil Nadu, India.

Nanotechnology Research Centre, SRM Institute of Science and Technology, Kattankulathur, Kancheepuram 603203, Tamil Nadu, India.

出版信息

ACS Omega. 2020 Jul 27;5(31):19747-19759. doi: 10.1021/acsomega.0c02477. eCollection 2020 Aug 11.

Abstract

A carbon dot (CD)-intercalated NiFeO (NFO)/graphitic carbon nitride (g-CN, g-CN) ternary Z-scheme heterojunction was synthesized by the facile wet chemical method and used for photo-Fenton degradation. The structural, optical, electrical, vibrational, and morphological properties of the photocatalysts were investigated through various analytical methods. The CD-intercalated heterojunction formation was analyzed by high-resolution transmission electron microscopy (HRTEM). The intercalated CD acted as an electron donor/acceptor, which converted a type-II heterojunction to a Z-scheme heterojunction. The formation of Z-scheme heterojunction was confirmed by the enormous production of radicals (hydroxyl (OH) and superoxide (O )) and the elemental trapping experiment. In particular, the heterojunction photocatalyst NFO/5g-CN/7.5CD showed the highest photo-Fenton degradation efficiency of 99% for rhodamine B (Rh B) and 93% for tetracycline (TCN) in the presence of HO. The charge separation and electron transport behaviors of the photocatalyst were examined by photoluminescence (PL) and photocurrent measurements. In the Z-scheme photo-Fenton system, hydroxyl and superoxide radicals played a vital role in the visible-light-driven degradation process. Hence, the prepared Z-scheme ternary photocatalyst is well suitable for wastewater treatment in practical use.

摘要

通过简便的湿化学方法合成了一种碳点(CD)插层的NiFeO(NFO)/石墨相氮化碳(g-CN)三元Z型异质结,并将其用于光芬顿降解。通过各种分析方法研究了光催化剂的结构、光学、电学、振动和形态性质。通过高分辨率透射电子显微镜(HRTEM)分析了CD插层异质结的形成。插层的CD充当电子供体/受体,将II型异质结转变为Z型异质结。自由基(羟基(OH)和超氧阴离子(O ))的大量产生和元素捕获实验证实了Z型异质结的形成。特别是,异质结光催化剂NFO/5g-CN/7.5CD在HO存在下对罗丹明B(Rh B)的光芬顿降解效率最高,为99%,对四环素(TCN)的降解效率为93%。通过光致发光(PL)和光电流测量研究了光催化剂的电荷分离和电子传输行为。在Z型光芬顿体系中,羟基和超氧阴离子自由基在可见光驱动的降解过程中起着至关重要的作用。因此,所制备的Z型三元光催化剂非常适合实际废水处理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b9f/7424713/919aabac28ae/ao0c02477_0001.jpg

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