One-pot synthesis of flower-like Bi2WO6/BiOCOOH microspheres with enhanced visible light photocatalytic activity

被引:9
|
作者
Liu, Min [1 ]
Lu, Mengjie [2 ]
Xie, Huihui [2 ]
Fu, Xiaojuan [2 ]
Wang, Yao [3 ]
Zhang, Weidong [4 ]
Xie, Yahong [1 ]
Qi, Ying [1 ]
机构
[1] Xinjiang Univ, Sch Chem Engn & Technol, Key Lab Petr & Nat Gas Fine Chem, Urumqi 830046, Peoples R China
[2] Xinjiang Univ, Sch Chem, Key Lab Petr & Nat Gas Fine Chem, Urumqi 830046, Peoples R China
[3] Chinese Acad Sci, Xinjiang Inst Ecol & Geog, Urumqi 830011, Peoples R China
[4] Qinghai Univ, Sch Chem Engn, Xining 810016, Peoples R China
关键词
Bi2WO6/BiOCOOH nanoparticles; Visible light nanophotocatalysts; Tetracycline; Antibiotics photodegradation; Semiconductors heterojunction; HETEROJUNCTION PHOTOCATALYSTS; CONSTRUCTION; NANOPARTICLES; COMPOSITE; REMOVAL; BI2WO6;
D O I
10.1016/j.seppur.2022.121920
中图分类号
TQ [化学工业];
学科分类号
0817 ;
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 (center dot O-2(-)) 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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页数:11
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