光催化
光电流
可见光谱
异质结
电子顺磁共振
吸收边
吸收(声学)
降级(电信)
化学工程
激进的
材料科学
光化学
化学
带隙
催化作用
光电子学
有机化学
复合材料
工程类
电信
物理
核磁共振
计算机科学
作者
Min Liu,Mengjie Lu,Huihui Xie,Xiaojuan Fu,Yao Wang,Weidong Zhang,Ya-Hong Xie,Ying Qi
标识
DOI:10.1016/j.seppur.2022.121920
摘要
Herein, flower-like Bi2WO6/BiOCOOH heterojunction photocatalysts were synthesized by one-pot method. Morphological characterizations had demonstrated that the Bi2WO6 nanoparticles were tightly anchored on the surface of BiOCOOH, which indicated that the successful synthesis of the Bi2WO6-BiOCOOH photocatalysts. Compared with pure BiOCOOH and Bi2WO6, the Bi2WO6/BiOCOOH photocatalysts had exhibited a red shift in absorption edge and enhanced visible light absorption. EIS, PL and photocurrent response results suggested that the form of the Bi2WO6-BiOCOOH heterojunction facilitated the separation of photogenerated electron and hole pairs. Furthermore, the photoactivity of Bi2WO6/BiOCOOH were evaluated by the photocatalytic degradation of tetracycline (TC) and ciprofloxacin (CIP) under the simulated sunlight irradiation. The results manifested that the W/Bi-2 photocatalyst exhibited the best photocatalytic activity, which TC was degraded by 88 % within 75 min and CIP was degraded by 90 % within 90 min. The improvement of photocatalytic activity was mainly attributed to the decrease in the composite rate of photo-induced electron-hole pairs. Radical trapping experiments and EPR results indicated that holes (h+) and superoxide radicals (·O2–) were dominant during the degradation of TC. The possible photocatalytic mechanism was discussed based on the band structures of BiOCOOH and Bi2WO6.
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