石墨氮化碳
量子点
材料科学
异质结
光催化
氮化碳
制氢
氮化物
光热治疗
纳米技术
肖特基势垒
多孔性
碳纤维
化学工程
氢
光电子学
复合数
催化作用
化学
复合材料
图层(电子)
有机化学
工程类
二极管
生物化学
作者
Jinghua Li,Hao Peng,Bing Luo,Jiamei Cao,Lijing Ma,Dengwei Jing
标识
DOI:10.1016/j.jcis.2023.03.015
摘要
A new heterostructure between Ti3C2 MXene quantum dot and 3D macroscopic porous graphitic carbon nitride (PGCN) was successfully obtained by integrating Ti3C2 quantum dots onto porous graphitized carbon nitride (Ti3C2QDs/PGCN) using in situ electrostatic self-assembly techniques. The photocatalytic H2 evolution rate of optimized 5.5 wt% Ti3C2 QD/PGCN composites is nearly 15.24 and 3.53 times higher than pristine CN, and PGCN, respectively. Ti3C2 quantum dots can significantly enhance the hydrogen production activity of PGCN. In addition, their good photothermal conversion ability accelerates the overall reaction process and enhances the light absorption and carrier density. Furthermore, to elucidate the photocatalytic mechanism, a series of tests involving electron spin resonance (ESR) and density functional theory (DFT) calculations were performed. The results confirmed that the Schottky barrier between PGCN and Ti3C2 QD can effectively promote spatial charge separation and significantly improve the photocatalytic performance. This work provides a new approach for the construction of photocatalytic systems and the application of MXene QD.
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