Prussian blue-conjugated ZnO nanoparticles for near-infrared light-responsive photocatalysis

光催化 材料科学 吸光度 普鲁士蓝 可见光谱 纳米颗粒 带隙 光化学 氧化物 纳米技术 亚甲蓝 光电子学 电化学 光学 有机化学 催化作用 物理化学 化学 冶金 物理 电极
作者
Hira Fatima,Muhammad Rizwan Azhar,Mehdi Khiadani,Yijun Zhong,Wei Wang,Chao Su,Zongping Shao
出处
期刊:Materials Today Energy [Elsevier]
卷期号:23: 100895-100895 被引量:35
标识
DOI:10.1016/j.mtener.2021.100895
摘要

Zinc oxide (ZnO)-based photocatalysis has great potential in wastewater treatment, but its photocatalytic performance suffers from the limitation of low-wavelength photon absorption. Herein, a near-infrared-responsive photocatalyst is developed to tackle this challenge, which is composed of Prussian blue (PB) dye conjugated iron oxide-zinc oxide hybrid nanoparticles (Fe3O4@[email protected]) with spherical morphology (∼14 nm). Fe3O4@[email protected] shows a higher-wavelength absorbance region centered at 781 nm as compared with PB-free Fe3O4-ZnO composite (Fe3O4@ZnO, 494 nm) and pristine ZnO (361 nm). The inclusion of a charge transfer band (FeII-CN-FeIII) after the conjugation of PB is responsible for such a profound absorbance shift. A comparative study of three samples as potential photocatalysts is performed in terms of the methylene blue degradation, which is found to be in an order of Fe3O4@[email protected] ˃ Fe3O4@ZnO ˃ ZnO. The enhanced photocatalysis rate of Fe3O4@[email protected] is credited to the lower bandgap of 1.2 eV from the presence of PB with low bandgap, retarded the recombination rate of electron-hole pair to produce enough reactive oxygen species from the rich surface vacancies and hole scavenging properties of PB. A plausible degradation mechanism of photocatalysis is proposed, revealing the singlet oxygen as the central point of enhanced performance.
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