Jiang Enhui, Liu Xiaoteng, Che Huinan, Liu Chunbo, Dong Hongjun, Che Guangbo
School of Chemistry and Chemical Engineering, Jiangsu University Zhenjiang 212013 P. R. China.
Institute of Green Chemistry and Chemical Technology, School of Chemistry and Chemical Engineering, Jiangsu University Zhenjiang 212013 P. R. China.
RSC Adv. 2018 Nov 5;8(65):37200-37207. doi: 10.1039/c8ra07482h. eCollection 2018 Nov 1.
In this study, a novel Ag/BiOCl photocatalyst has been synthesized by a facile photodeposition process. Its photocatalytic performance was evaluated from the degradation of tetracycline (TC) under visible light irradiation ( > 420 nm). The 1.0 wt% Ag/BiOCl photocatalyst could significantly enhance the degradation of TC compared with pure BiOCl, with the degradation level reaching 94.2% in 120 minutes. The enhancement of photocatalytic activity could be attributed to the synergetic effect of the photogenerated electrons (e) of BiOCl and the surface plasmon resonance (SPR) caused by Ag nanoparticles, which could improve the absorption capacity of visible light and facilitate the separation of photogenerated electron-hole pairs. In addition, electron spin resonance (ESR) analysis and trapping experiments demonstrated that the superoxide radicals (˙O), hydroxyl radicals (˙OH) and holes (h) played crucial roles in the photocatalytic process of TC degradation. The present work provides a promising approach for the development of highly efficient photocatalysts to address current environmental pollution, energy issues and other related areas.
在本研究中,通过简便的光沉积法合成了一种新型的Ag/BiOCl光催化剂。在可见光(>420 nm)照射下,通过四环素(TC)的降解来评估其光催化性能。与纯BiOCl相比,1.0 wt%的Ag/BiOCl光催化剂能显著提高TC的降解率,120分钟内降解率达到94.2%。光催化活性的提高可归因于BiOCl光生电子(e)与Ag纳米颗粒引起的表面等离子体共振(SPR)的协同效应,这可以提高可见光的吸收能力并促进光生电子-空穴对的分离。此外,电子自旋共振(ESR)分析和捕获实验表明,超氧自由基(˙O)、羟基自由基(˙OH)和空穴(h)在TC降解的光催化过程中起关键作用。目前的工作为开发高效光催化剂以解决当前环境污染、能源问题及其他相关领域提供了一种有前景的方法。
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