Fabrication of a novel BiOI/KTaO3 p-n heterostructure with enhanced photocatalytic performance under visible-light irradiation

被引:15
|
作者
Lu, Xiaoxiao [1 ,2 ]
Li, Qiang [1 ,2 ]
Liu, Shihao [1 ,2 ]
Luo, Rui [1 ,2 ]
Li, Hong [1 ,2 ]
Zhang, Min [1 ,2 ]
Cui, Chaopeng [1 ,2 ]
Zhu, Guangping [1 ,2 ]
Chen, San [1 ,2 ]
Liang, Changhao [3 ]
机构
[1] Huaibei Normal Univ, Coll Phys & Elect Informat, Huaibei 235000, Peoples R China
[2] Huaibei Normal Univ, Anhui Prov Key Lab Pollutant Sensit Mat & Environ, Huaibei 235000, Peoples R China
[3] Chinese Acad Sci, Anhui Key Lab Nanomat & Nanotechnol, Inst Solid State Phys, Key Lab Mat Phys,Hefei Inst Phys Sci, Hefei 230031, Peoples R China
关键词
JUNCTION PHOTOCATALYSTS; DEGRADATION; DRIVEN; KTAO3; HETEROJUNCTION; COMPOSITE; STRATEGY; TIO2; NANOPARTICLES; EFFICIENCY;
D O I
10.1039/c9ra10231k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, a series of BiOI/KTaO3 p-n heterojunctions were prepared via a facile in situ chemical bath strategy. The photocatalytic properties of the catalysts was tested by the degradation of Rhodamine B (RhB) and phenol under visible light irradiation. The BiOI/KTaO3 composites exhibited improved photocatalytic efficiency compared to the individual catalysts. In particular, 54 wt% BiOI/KTaO3 displayed the highest photocatalytic activity since it degraded 98.6% RhB within 30 minutes, while only 68.1% RhB was degraded over pure BiOI under identical conditions. In addition, the reaction kinetic constant of RhB degradation over 54 wt% BiOI/KTaO3 was approximately 2.56 and 115-fold larger than those of pure BiOI and KTaO3, respectively. The results of PL, photocurrent and EIS indicated that the improved photocatalytic efficiency could root in the p-n junction formed between BiOI and KTaO3, which was conducive to the separation and migration of photo-generated carriers. Furthermore, a free-radical capture experiment illustrated that h(+) and O-center dot(2)- were the key factors in the photodegradation of RhB.
引用
收藏
页码:10921 / 10931
页数:11
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