Integration of biochar into Ag3PO4/α-Fe2O3 heterojunction for enhanced reactive oxygen species generation towards organic pollutants removal

• Published in: Environmental pollution (1987) 2022-06, Vol.303, p.119131-119131, Article 119131
• Main Authors: Qian, Yifan, Shi, Jun, Yang, Xianni, Yuan, Yangfan, Liu, Li, Zhou, Ganghua, Yi, Jianjian, Wang, Xiaozhi, Wang, Shengsen
• Format: Article
• Language: English
• Subjects: Ag3PO4; Biochar; Degradation of dye and antibiotics; Photocatalysis; α-Fe2O3
• ISSN: 0269-7491; 1873-6424
• DOI: 10.1016/j.envpol.2022.119131

A biochar (BC) harbored Ag3PO4/α-Fe2O3 type-Ⅰ heterojunction (Ag-Fe-BC) was prepared by a hydrothermal-impregnation method to transfer active center of heterojunctions. The electrochemical and spectroscopic tests demonstrated that BC enhanced the catalytic performance of the heterojunction by enhancing photocurrent, reducing fluorescence intensity, and facilitating separation of electron-hole pairs. The photocatalytic activity showed the Ag-Fe-BC (5:1:3) could degrade Rhodamine B (20 mg/L) by up to 92.7%, which was 3.35 times higher than Ag3PO4/α-Fe2O3. Tetracycline and ciprofloxacin (20 mg/L) were degraded efficiently by 58.3% and 79.4% within 2 h, respectively. Electron paramagnetic resonance and scavenging experiments confirmed the major reactive oxygen species (ROS) consisted of singlet oxygen (1O2) and superoxide (·O2−). Excellent RhB adsorption and electrons capturing capacity of BC facilitated electron-hole pairs separation and ROS transferring to target organics followed by elevated degradation. Thus, a facile method was proposed to synthesize a highly efficient visible-light responsive photocatalyst for degradation of various organics in water. •Ag-Fe-BC showed good catalytic performance towards organic pollutants.•Organics were mainly degraded by singlet oxygen and superoxide.•BC served as an electron acceptor and active center.•BC enhanced pollutant adsorption and ROS-driven degradation of dye and antibiotics.