Conversion of a Type-II to a Z-Scheme Heterojunction by Intercalation of a 0D Electron Mediator between the Integrative NiFe2O4/g-C3N4 Composite Nanoparticles: Boosting the Radical Production for Photo-Fenton Degradation

被引:125
|
作者
Palanivel, Baskaran [1 ,2 ]
Mani, Alagiri [1 ]
机构
[1] SRM Inst Sci & Technol, Dept Phys & Nanotechnol, Kancheepuram 603203, Tamil Nadu, India
[2] SRM Inst Sci & Technol, Nanotechnol Res Ctr, Kancheepuram 603203, Tamil Nadu, India
来源
ACS OMEGA | 2020年 / 5卷 / 31期
关键词
CARBON QUANTUM DOTS; PHOTOCATALYTIC ACTIVITY; NANOCOMPOSITES; FABRICATION; REMOVAL; HYBRIDS; TIO2;
D O I
10.1021/acsomega.0c02477
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A carbon dot (CD)-intercalated NiFe2O4 (NFO)/graphitic carbon nitride (g-C3N4, 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 Zscheme heterojunction. The formation of Z-scheme heterojunction was confirmed by the enormous production of radicals (hydroxyl (OH center dot) and superoxide (O-2(-))) 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 H2O2. 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.
引用
收藏
页码:19747 / 19759
页数:13
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