光催化
纳米片
盐酸四环素
降级(电信)
兴奋剂
可见光谱
四环素
材料科学
核化学
化学工程
光化学
化学
光电子学
纳米技术
催化作用
有机化学
计算机科学
电信
工程类
生物化学
抗生素
作者
Huabing Zhang,Wenxin Luo,Houxiang Sun,Haiyan Yang,Tao Yang,Dongqi Liu,Xuejun Zhu,Lihua Zhao,Mingyong Shu,Fengli Yang
标识
DOI:10.1021/acsanm.4c01096
摘要
In this paper, a facile and efficient photocatalytic system for tetracycline hydrochloride (TCH) degradation is proposed. Ce-doped Bi2WO6 (Ce–Bi2WO6) nanosheets rich in oxygen vacancies were synthesized using a simple hydrothermal method and were systematically characterized. The results exhibited that a 10% Ce–Bi2WO6 (BWCe-10) catalyst with thinner and curling nanosheets was rich in oxygen vacancies, and the band gap was narrowed from 2.78 eV (Bi2WO6) to 1.61 eV, which was conducive to enhancing the photocatalytic activity of BWCe-10. As expected, BWCe-10 nanosheets exhibited much higher photocatalytic performance with 61.1% degradation of TCH within 40 min due to the formation of oxygen vacancies. Moreover, the addition of H2O2 further enhanced the TCH degradation efficiency and yielded a removal rate of 90.4%, revealing a strong synergistic effect between oxygen vacancies and H2O2 in the BWCe-10/H2O2/light system. As an electron acceptor, H2O2 boosts the separation rate of the photogenerated carriers, thereby improving the photocatalytic activity. Furthermore, the potential applications of the BWCe-10 nanosheet in terms of the effect of coexisting ions, stability, and universality were investigated. In addition, possible degradation mechanisms and pathways were proposed. In this system, h+ and e– played important roles in TCH degradation and followed the sequence h+/e– > •O2– > •OH, and the formation of •OH and •O2– was proved by ESR analysis. This simulated sunlight-driven system offers insights into the degradation of organic contaminants.
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