0D boron carbon nitride quantum dots decorated 2D Bi4O5I2 as 0D/2D efficient visible-light-driven photocatalysts for tetracyclines photodegradation

被引:21
作者
Xu, Kailin [1 ]
Zhang, Qiuya [1 ]
Wang, Chuqiao [2 ]
Xu, Jinmei [3 ]
Bu, Yiming [1 ]
Liang, Bin [1 ]
Liu, Yushuai [1 ]
Wang, Liping [1 ,3 ]
机构
[1] Changzhou Univ, Sch Environm & Safety Engn, Changzhou 213164, Peoples R China
[2] East China Jiaotong Univ, Sch Civil Engn & Architecture, Nanchang 330013, Jiangxi, Peoples R China
[3] Changzhou Univ, Huaide Coll, Jingjiang 214500, Peoples R China
基金
中国国家自然科学基金;
关键词
Bi4O5I2; Boron carbon nitride quantum dots; Tetracyclines; 0D/2d heterojunction; Photocatalysis; DEGRADATION PATHWAYS; REACTION-MECHANISM; FACILE SYNTHESIS; WATER; REMOVAL; OXYTETRACYCLINE; ANTIBIOTICS; IRRADIATION; FABRICATION; ADSORPTION;
D O I
10.1016/j.chemosphere.2021.133230
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A series of 0D boron carbon nitride quantum dots (BCNQDs) modified 2D Bi4O5I2 (0D/2D Bi4O5I2/BCNQDs) composites were synthesized and applied to photodegradation of tetracyclines (TCs), including tetracycline (TC) and oxytetracycline (OTC). The Bi4O5I2/BCNQDs (1) (1 mL BCNQDs) composite exhibits the highest photo catalytic performance for TCs degradation. The degradation rate constants of TC and OTC by the optimal sample were 4.95 and 2.17 times that of Bi4O5I2, respectively. This can be attributed to the fact that the narrow bandgap Bi4O5I2 is the electron acceptor, and the oxygen-containing functional group with the negative charge on BCNQDs can promote the formation of photoexcited holes, which makes the effective separation of photoexcited carriers easier. Furthermore, the active substance (h(+) and .O2-) is the major active substance for TCs photo degradation. On this basis, the possible photocatalytic reaction mechanism of Bi4O5I2/BCNQDs (1) composite is proposed. This study provides a new idea for 0D/2D interface engineering of BCNQDs heterojunction.
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页数:12
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