g-C3N4-modified BiOCl as a visible light catalyst and its enhanced photocatalytic degradation/sterilization performance

被引:0
作者
Su, Yu [1 ]
Gao, Zheng [1 ]
Zhang, Lei [1 ,2 ]
Zhang, Bo [1 ,2 ]
Xu, Rui [1 ,2 ]
Cheng, Xiang [1 ]
Li, Nansha [1 ]
Zhao, Wei [1 ,2 ]
机构
[1] Tianjin Chengjian Univ, Sch Mat Sci & Engn, Tianjin 300384, Peoples R China
[2] Tianjin Key Lab Bldg Green Funct Mat, Tianjin 300384, Peoples R China
基金
中国国家自然科学基金;
关键词
GRAPHITIC CARBON NITRIDE; CHARGE-TRANSFER; G-C3N4; PHOTODEGRADATION; NANOSHEETS; HETEROJUNCTIONS; PHOTOACTIVITY; BIOCL/G-C3N4; BAND; BR;
D O I
10.1039/d4cy01561d
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
In an effort to tackle the disadvantages of the narrow photo-responsive range and easy recombination of carriers in BiOCl materials, a simple calcination strategy was adopted to modify BiOCl with g-C3N4. BiOCl/g-C3N4 nanoplates with a high specific surface area (48.11 m2 g-1) and visible photoresponse were obtained. When BiOCl/g-C3N4 (mass ratio: 10 : 2) was used, the degradation rate of RhB exceeded 90% within 10 min, while the degradation of MO was completed within 3 h. In addition, 91.35% of the sulfur-oxidizing bacteria could be eliminated. The sheet-to-sheet intercalation structure formed between g-C3N4 and BiOCl not only led to an increase in specific surface area but also facilitated electron transfer and carrier separation through the BiOCl/g-C3N4 heterojunction. In addition to these experimental evidence, the efficient utilization of solar energy and remarkable separation of photogenerated carriers, confirmed by energy band regulation and significant electron accumulation in the heterojunction (as provided by DFT calculations), contribute to the superior catalytic performance of the BiOCl/g-C3N4 heterojunction.
引用
收藏
页码:2261 / 2271
页数:11
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