Facile fabrication of 3D hollow porous aminopyridine rings decorated polymeric carbon nitride for enhanced photocatalytic hydrogen evolution and dye elimination

光催化 催化作用 三聚氰胺 化学工程 材料科学 降级(电信) 氮化碳 复合数 制氢 石墨氮化碳 光化学 化学 复合材料 有机化学 电信 工程类 计算机科学
作者
Dong Liu,Congyue Zhao,Chunling Li,Jiaojiao Jia,Ming‐Hui Chen,Likun Pan,Yichun Bai,Weidong Wu,Tianjun Ni
出处
期刊:Journal of Colloid and Interface Science [Elsevier]
卷期号:649: 334-343 被引量:4
标识
DOI:10.1016/j.jcis.2023.06.128
摘要

In consideration of energy shortages and environmental pollution, there is a critical need to develop a photocatalyst with high catalytic performance for rapid hydrogen production and efficient pollutant degradation. We synthesized a photocatalytic composite catalyst with three-dimensional (3D) porous aminopyridine rings grafted on the edge of g-C3N4 (APCN) using melamine, cyanuric acid and 4-aminopyridine as raw materials. The composite catalyst exhibited excellent photocatalytic performance for H2 production (2.44 mmol g−1h−1) and RhB degradation (97.08%) under visible light. Subsequently, a possible enhanced mechanism of the catalyst was proposed on the basis of a series of characterization and photocatalytic experiments. The 3D porous structure not only enhanced the structural stability but also increased the surface area of the APCN catalysts, which generated more exposed active sites. Moreover, the aminopyridine ring embellishment was beneficial for achieving a narrowed bandgap and charge migration and separation, which decreased the occurrence of photogenerated carrier recombination. In summary, these two structural features showed a synergistic effect to enhance the photocatalytic performance of the APCN catalyst. Finally, an integrated feasible enhanced mechanism of photocatalytic activity was elucidated according to the results of active substance capture tests, showing that O2•− played an important role during RhB degradation.
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