降级(电信)
石墨氮化碳
制氢
光催化
氢
污染物
氮化碳
氮气
碳纤维
材料科学
可见光谱
氮化物
兴奋剂
化学工程
环境化学
环境科学
光化学
化学
催化作用
纳米技术
光电子学
计算机科学
有机化学
电信
复合材料
工程类
生物化学
复合数
图层(电子)
作者
Jun Hu,Chenghui Hu,Hongyin Liu,Feipeng Jiao
标识
DOI:10.1021/acs.iecr.4c04688
摘要
The photocatalytic activity of graphitic carbon nitride (g-C3N4) is always constrained by rapid carrier recombination, a low specific surface area, and narrowed light response. In this study, nitrogen self-doped g-C3N4 (NCN) with optimized band structure was successfully fabricated by the copolymerization of a mixture including melamine and ethylenediamine. The resultant samples were perfectly applied to the photocatalytic hydrogen production and photodegradation of tetracycline. Characterizations and density functional theory (DFT) calculations identified the introduction of a nitrogen doping site within the g-C3N4 framework. The narrowed band gap, limited photoinduced carrier recombination, and rapid charge transfer were attributed to the DFT, optical properties, and photoelectrochemical analysis, which improved the visible light absorption and optimized the carrier migration channel. Specifically, NCN6 exhibited a 13.47 times higher hydrogen evolution rate (3.07 mmol g–1 h–1) with an apparent quantum yield of 12.65% at 420 nm and 1.78-fold (82.49%) better photodegradation efficiencies than pristine g-C3N4 (0.23 mmol g–1 h–1 and 58.79%), respectively. This study offers a straightforward approach to the synthesis of functionalized g-C3N4, with the objective of enhancing the photocatalytic activity and elucidating the doping mechanism. Furthermore, it provides guidance for the development of nonmetal-doped organic semiconductor photocatalysts.
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