Heterostructural Ag3PO4/UiO-66 composite for highly efficient visible-light photocatalysts with long-term stability

被引:48
作者
Zhang, Na [1 ]
Zhang, Xiaolei [1 ]
Gan, Chuanxian [1 ]
Zhang, Jianyong [1 ,2 ]
Liu, Yufeng [1 ]
Zhou, Min [2 ]
Zhang, Cheng [1 ]
Fang, Yongzheng [1 ]
机构
[1] Shanghai Inst Technol, Shanghai 201418, Peoples R China
[2] Southeast Univ, Sch Mat Sci & Engn, Nanjing 211189, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Heterostructure photocatalyst; Metal-organic-frameworks; Synergistic effect; METAL-ORGANIC FRAMEWORKS; HYDROGEN-PRODUCTION; DEGRADATION; OXIDATION; AG3PO4; SEMICONDUCTOR; MICROCRYSTALS; OCTAHEDRONS; MECHANISM; OXIDE;
D O I
10.1016/j.jphotochem.2019.03.025
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
To aim to extent the advantage of the high optical absorbance and overcome the shortcoming of the instability on Ag3PO4, a novel visible-light-driven heterostructure photocatalyst Ag3PO4/UiO-66 (APU) composite with a synergistic effect of adsorption enrichment and photocatalysis degradation has been successfully fabricated via a facile chemical bath deposition method. The APU photocatalyst is not only favorable to increasing the absorption ability for organic pollutants owing to a larger surface area, but also promotes the separation and transformation of electron-hole pairs due to the good conductivity performance in the presence of Ag/Ag3PO4/UiO-66 structure. Under visible-light illumination, the APU-15% composite photocatalyst has exhibited the excellent removal capacity, and the degradation efficiency can be up to 100% in 18 min. The degradation constant are about 80 and 2.7 times higher than those of bare UiO-66 and Ag3PO4 for the removal of RhB in the dynamic system, respectively. The enhancement of removal efficiency is due to a synergistic effect of adsorption enrichment and photocatalysis degradation. The removal rate of the APU-15% composite photocatalyst has only 9.5% decrease for 5 cycles of the photoreaction, showing the relatively good stability. The trapping experiment and ESR show the main active species is O2(center dot)(-). Furthermore, the photocatalytic mechanism has been proposed in the end.
引用
收藏
页码:305 / 315
页数:11
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