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Synthesis of WO3 nanofibers decorated with BiOCl nanosheets for photocatalytic degradation of organic pollutants under visible light

Journal 2019 · IF 3.131 · 发表于 2019 年 8 月 6 日
作者: Yi Xiao,Zeqing He,Renshan Wang,Xueqin Tao,Benxia Li
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摘要

Notwithstanding intensive research in recent decades, the conspicuous restrictions in photocatalysts still remain as low utilization of visible light, poor charge transfer/separation, and insufficient surface active sites. Designing semiconductor heterostructures as photocatalysts is a promising approach to enhance the photocatalytic efficiency for degrading organic pollutants. In this work, a novel WO 3 /BiOCl p–n heterostructure photocatalyst with optimal molar ratio was successfully fabricated by growing BiOCl nanosheets on WO 3 nanofibers through the electrospinning method followed with a solvothermal process. The optical properties and photoelectrochemical tests indicated that the WO 3 /BiOCl heterostructures possess high ability of photogenerated charge separation. The photocatalytic performance of the as-obtained materials was assessed by the degradations of rhodamine B (RhB) and phenol in water under visible light. Compared with pure WO 3 nanofibers and BiOCl nanosheets, the WO 3 /BiOCl heterostructure catalysts showed improved photocatalytic efficiencies, and the apparent rate constant of RhB degradation is 0.259 min −1 on the optimal WO 3 /BiOCl(2) sample, which is about 2.3 times that of pure BiOCl (0.113 min −1 ). The roles of different active species in the photocatalytic system were determined by active-species-eliminating experiments, revealing that the photogenerated holes play a leading function in the degradation of organic pollutants. The enhanced photocatalysis of WO 3 /BiOCl(2) heterostructures results from the joint effect of high activity of BiOCl nanosheets, anti-agglomeration of WO 3 nanofibers, and well-matched straddling band-structures for charge separation. This photocatalyst presents great potential in the removal of organic pollutants from aquatic environment.

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