光催化
异质结
降级(电信)
催化作用
材料科学
石墨氮化碳
化学工程
产量(工程)
磷
化学
光化学
光电子学
复合材料
有机化学
计算机科学
工程类
电信
冶金
作者
Jiaqi Li,Yuqing Mei,Shouchun Ma,Qing‐Feng Yang,Baojiang Jiang,Baifu Xin,Tongjie Yao,Jie Wu
标识
DOI:10.1016/j.jcis.2021.10.119
摘要
Herein, a type-I phosphorus-doped carbon nitride/oxygen-doped carbon nitride (P-C3N4/O-C3N4) heterojunction was designed for photocatalysis-self-Fenton reaction (photocatalytic H2O2 production and following Fenton reaction). In P-C3N4/O-C3N4, the photoinduced charge carriers were effectively separated with the help of internal-electric-field near the interface, ensuring the high catalytic performance. As a result, the production rate of H2O2 in an air-saturated solution was 179 μM·h-1, about 7.2, 2.5, 2.5 and 2.1 times quicker than that on C3N4, P-C3N4, O-C3N4, and phosphorus and oxygen co-doped C3N4, respectively. By taking advantage of the cascade mode in photocatalysis-self-Fenton reaction, H2O2 utilization efficiency was remarkably improved to 77.7%, about 9.0 times higher than that of traditional homogeneous Fenton reaction. Befitting from the superior yield and utilization efficiency, the degradation performance of P-C3N4/O-C3N4 was undoubtedly superior than other photocatalysts. This work well addressed two bottlenecks in traditional Fenton reaction: source of H2O2 and their low utilization efficiency, and the findings were beneficial to understand the mechanism and advantage of the photocatalysis-self-Fenton system in environmental remediation.
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