Enhancing photodegradation activity of g-C3N4 via decorating with S-doped carbon nitride quantum dots by in situ polymerization

被引:33
|
作者
Li, Hongling [1 ]
Huang, Guozhi [1 ]
Xu, Huazhen [1 ]
Yang, Zhiqing [1 ]
Xu, Xinmei [1 ]
Li, Jinyu [2 ]
Qu, Ailan [1 ,3 ]
Chen, Yao [1 ]
机构
[1] Jinan Univ, Chem & Mat Sch, 601 West Huangpu Rd, Guangzhou 510632, Peoples R China
[2] Yale Univ, Physiol Dept, New Haven, CT 06511 USA
[3] XINGFULE Biotechnol Co Ltd, Fuzhou 362200, Fujian, Peoples R China
关键词
Nonmetallic quantum dots; Graphitic carbon nitride; In situ polymerization; Photocatalytic activity; VISIBLE-LIGHT; FACILE SYNTHESIS; PHOTOCATALYTIC ACTIVITY; CONTROLLABLE SYNTHESIS; METHYL-ORANGE; SURFACE-AREA; RHODAMINE-B; SULFUR; DEGRADATION; WATER;
D O I
10.1016/j.jssc.2020.121705
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In this work, sulfur doped carbon nitride quantum dots (S-CNQDs) were prepared by one-pot copolymerization using melamine and thiourea as starting materials. The composite (g-C3N4/S-CNQDs), showing enlarged surface area, was fabricated by one-step in situ polymerization. The composites displayed much better photocatalytic activity than pristine g-C3N4 in degradation of methyl orange (MO) under UV-visible light irradiation. The removal efficiency of MO reached by 94.3% under visible light (lambda > 420 nm) illumination within 80 min, whereas it was nearly 100% under UV-visible light (lambda > 350 nm) irradiation within 40 min. The enhanced photocatalytic activity of composites is attributed to the doping of S-CNQDs, which leads to higher separation of photo-generated electron-holes, extended visible light response and more active sites. Additionally, the potential mechanism of photocatalytic degradation on MO by g-C3N4/S-CNQDs was proposed. This work presented a simple way for constructing S-CNQDs-based g-C(3)N(4 )catalyst.
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页数:14
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