光催化
光降解
石墨氮化碳
可见光谱
X射线光电子能谱
化学
光化学
傅里叶变换红外光谱
扫描电子显微镜
高分辨率透射电子显微镜
光致发光
氮化碳
核化学
材料科学
化学工程
透射电子显微镜
纳米技术
催化作用
有机化学
光电子学
复合材料
工程类
作者
Pankaj Raizada,Prachi Thakur,Anita Sudhaik,Pardeep Singh,Vijay Kumar Thakur,Ahmad Hosseini–Bandegharaei
标识
DOI:10.1016/j.arabjc.2019.10.001
摘要
Advances in noble metal mediated Z-scheme photocatalytic system have ushered in a climax on environmental remediation. Herein, graphitic carbon nitride (GCN) and phosphorus sulphur co-doped graphitic carbon nitride (PSCN) were synthesized via calcination process. GCN, PSCN and Z-scheme visible light driven (VLD) ternary BiOBr/PSCN/Ag/AgCl nanophotocatalyst were characterized by X-ray diffraction pattern (XRD), Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and UV–visible diffuse reflectance spectra (UV–vis DRS). BiOBr/PSCN/Ag/AgCl nanocomposite exhibited superior visible light driven photocatalytic ability as compared to pristine PSCN, AgCl and BiOBr towards degradation of phenol. The results explicated promising photocatalytic activity along with space separation of photocarriers caused via formation of BiOBr/PSCN/Ag/AgCl Z-scheme heterojunction. The visible light absorption efficacy of BiOBr/PSCN/Ag/AgCl photocatalyst was confirmed by photoluminescence (PL) spectra. Finally, recycling experiments were explored for the mechanistic detailing of phenol photodegradation employing BiOBr/PSCN/Ag/AgCl photocatalyst. After seven successive cycles photodegradation efficacy of photocatalyst was reduced to 90% from 98%. Proposed mechanism of BiOBr/PSCN/Ag/AgCl nanophotocatalyst for degradation of phenol was discussed. OH and O2− radicals were main reactive species responsible for photocatalytic phenol degradation.
科研通智能强力驱动
Strongly Powered by AbleSci AI