Molecular engineering of polymeric carbon nitride for highly efficient photocatalytic oxytetracycline degradation and H2O2 production

被引:359
作者
Yang, Yang
Zeng, Guangming [1 ]
Huang, Danlian [1 ]
Zhang, Chen [1 ]
He, Donghui
Zhou, Chengyun
Wang, Wenjun
Xiong, Weiping
Li, Xiaopei
Li, Bisheng
Dong, Wanyue
Zhou, Yin
机构
[1] Hunan Univ, Coll Environm Sci & Engn, Changsha 410082, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon nitride; Molecular engineering; Photocatalysis; Oxytetracycline degradation; H2O2; production; HYDROGEN-PEROXIDE PRODUCTION; HETEROJUNCTION PHOTOCATALYSTS; CHARGE-TRANSFER; WASTE-WATER; G-C3N4; TETRACYCLINE; ENERGY; OXYGEN; REDUCTION; EVOLUTION;
D O I
10.1016/j.apcatb.2020.118970
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
Developing highly efficient photocatalysts for refractory pollutants degradation and hydrogen peroxide (H2O2) production is an ideal strategy to tackle environmental pollution and energy crisis. Herein, we synthesize a novel 2-hydroxy-4,6-dimethylpyrimidine (HDMP) grafted polymeric carbon nitride (CN) photocatalyst (ACN) by a facile in situ keto-enol cyclization method for addressing these issues. The photogenerated electrons and holes are migrated to HDMP and heptazine moiety, respectively. And the average decay lifetime of photogenerated charges of CN and ACN-10 is increased form (222 +/- 23) to (289 +/- 38) ps. Benefiting from the controllable electronic migration and accelerated intramolecular charge separation, the ACN photocatalyst exhibits a superior visible-light-driven photocatalytic activity for oxytetracycline degradation and H2O2 production. This work makes an insight into the intramolecular charge dynamics in CN, and presents a promising approach to the oxytetracycline degradation and H2O2 production.
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页数:14
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