Xu Yongzhang, Luo Xingrui, Wang Fulin, Xiang Wentao, Zhou Chensheng, Huang Weiya, Lu Kangqiang, Li Shaoyu, Zhou Man, Yang Kai
Jiangxi Provincial Key Laboratory of Functional Molecular Materials Chemistry, School of Chemistry and Chemical Engineering, Jiangxi University of Science and Technology, Ganzhou 341000, China.
Jiangxi Provincial Engineering Technology Research Center for Electronic Chemicals of Printed Circuit Boards, Ganzhou 341000, China.
Molecules. 2024 Sep 4;29(17):4196. doi: 10.3390/molecules29174196.
The development of efficient and environmentally friendly photocatalysts is crucial for addressing global energy and environmental challenges. Perylene diimide, an organic supramolecular material, holds great potential for applications in mineralized phenol. In this study, through the integration of different mass ratios of unmodified perylenimide (PDI-NH) into the self-assembly of amino acid-substituted perylenimide (PDI-COOH), a novel supramolecular organic heterojunction (PDICOOH/PDINH) was fabricated. The ensuing investigation focuses on its visible-light mineralized phenol properties. The results show that the optimal performance is observed with a composite mass fraction of 10%, leading to complete mineralization of 5 mg/L phenol within 5 h. The reaction exhibits one-stage kinetics with rate constants 13.80 and 1.30 times higher than those of PDI-NH and PDI-COOH, respectively. SEM and TEM reveal a heterogeneous interface between PDI-NH and PDI-COOH. Photoelectrochemical and Kelvin probe characterization confirm the generation of a built-in electric field at the interface, which is 1.73 times stronger than that of PDI-COOH. The introduction of PDI-NH promotes π-π stacking of PDI-COOH, while the built-in electric field facilitates efficient charge transfer at the interface, thereby enhancing phenol decomposition. The finding demonstrates that supramolecular heterojunctions have great potential as highly effective photocatalysts for environmental remediation applications.
开发高效且环保的光催化剂对于应对全球能源和环境挑战至关重要。苝二亚胺作为一种有机超分子材料,在矿化苯酚方面具有巨大的应用潜力。在本研究中,通过将不同质量比的未改性苝酰亚胺(PDI-NH)融入氨基酸取代苝酰亚胺(PDI-COOH)的自组装过程,制备了一种新型超分子有机异质结(PDI-COOH/PDI-NH)。随后的研究聚焦于其可见光矿化苯酚的性能。结果表明,当复合质量分数为10%时观察到最佳性能,可在5小时内使5 mg/L苯酚完全矿化。该反应呈现一级动力学,速率常数分别比PDI-NH和PDI-COOH高13.80倍和1.30倍。扫描电子显微镜(SEM)和透射电子显微镜(TEM)显示PDI-NH和PDI-COOH之间存在异质界面。光电化学和开尔文探针表征证实了界面处产生了内建电场,其强度比PDI-COOH强1.73倍。PDI-NH的引入促进了PDI-COOH的π-π堆积,而内建电场有助于界面处的高效电荷转移,从而增强了苯酚的分解。该发现表明超分子异质结作为用于环境修复应用的高效光催化剂具有巨大潜力。