A novel synergy of Er3+/Fe3+ co-doped porous Bi5O7I microspheres with enhanced photocatalytic activity under visible-light irradiation

光催化 光降解 材料科学 可见光谱 光化学 吸收边 光子上转换 激进的 苯酚 吸收(声学) 降级(电信) 兴奋剂 辐照 核化学 催化作用 光电子学 有机化学 化学 复合材料 物理 电信 带隙 核物理学 计算机科学
作者
Yongbao Liu,Gangqiang Zhu,Jianzhi Gao,Runliang Zhu,Mirabbos Hojamberdiev,Chenghui Wang,Xiumei Wei,Peng Liu
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:205: 421-432 被引量:132
标识
DOI:10.1016/j.apcatb.2016.12.061
摘要

Uniform porous Bi5O7I (BOI) microspheres photocatalysts co-doped with Fe3+ and Er3+ were synthesized by a solvothermal-thermal decomposition method, in which Er3+ with upconversion properties could transform infrared light beyond the absorption edge of Bi5O7I into visible light, and also activate the Fe3+-doped Bi5O7I (Fe-BOI). The photocatalytic activities of the photocatalysts were evaluated by the degradation of three typical colorless model pollutants, i.e., phenol, bisphenol A (BPA), and chloramphenicol (CAP), under visible light irradiation (800 nm > λ > 400 nm). The results showed that the photocatalytic activity of Fe3+/Er3+ co-doped Bi5O7I (Er/Fe-BOI) was much higher than that of the undoped, Fe3+-doped and Er3+-doped Bi5O7I photocatalysts. In addition, Fe3+/Er3+ co-doped Bi5O7I exhibited photocatalytic activity under a 3W LED lamp (red light, λ = 630 nm) with the wavelength beyond the absorption edge of Bi5O7I, which further testified that the upconversion effect of Er3+ generates the enhanced photocatalytic activity of Bi5O7I. Photodegradation mechanism was systematically studied by using various radical quenchers and it was revealed that photogenerated holes (h+) and superoxide radicals (O2−) actively participated, whereas hydroxyl (OH) radicals had negligible contribution in photodegradation of phenol.
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