光催化
兴奋剂
材料科学
带隙
罗丹明B
石墨氮化碳
吸收边
长石
氮化碳
纳米技术
光化学
化学工程
催化作用
化学
氧化物
光电子学
有机化学
工程类
冶金
作者
Yan Zheng,Yang Liu,Linlin Zhang,Jingde Luan,Xin Ke
出处
期刊:Langmuir
[American Chemical Society]
日期:2023-09-12
卷期号:39 (38): 13705-13716
被引量:4
标识
DOI:10.1021/acs.langmuir.3c01935
摘要
Constructing a nanostructure with a high surface area and regulating the band gap by nonmetallic doping are two effective methods for improving the photocatalytic activity of catalysts. A green template-free synthesis strategy of S-doped g-C3N4 nanosheets is proposed via doping cystine as both the structural additive and S source. The features of S-doped samples (GCN-x%) were systematically studied, including morphology and textural and photoelectric properties, which demonstrated that the introduction of cystine and simple manipulation of the preparation process could realize self-exfoliation of g-C3N4 into nanosheets. The GCN-3% sample showed a surface area (131.88 m2·g-1) 10.7 times enlarged compared with bulk g-C3N4 (bulk-phase carbon nitride). Obvious redshift on the absorption edge induced by S doping can be observed, revealing a narrowed band gap and enhanced efficiency of photogenerated charge carrier separation. The DFT calculation results also verified that the introduced C-S site could lead to polarization of the local electric field and thus decrease the bandgap of g-C3N4 nanosheets. GCN-3% showed a 99.3% photocatalytic degradation ratio of rhodamine B in 60 min at a rate of 0.17 min-1. By scavengers experiment revealed that superoxide anion (·O2-) radicals and holes (h+) were vital active components during the photocatalytic degradation.
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