化学
固氮
敏化
光催化
纳米-
氮气
固定(群体遗传学)
光化学
叶绿素
化学工程
催化作用
有机化学
生物化学
免疫学
工程类
基因
生物
作者
Yangyang Sun,Tianyu Huang,Wanchang Feng,Guangxun Zhang,Houqiang Ji,Ying Zhu,Huijie Zhou,Fei Dou,Yichun Su,Zheng Liu,Meifang Yang,Huan Pang
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-12-16
卷期号:63 (52): 24876-24884
被引量:2
标识
DOI:10.1021/acs.inorgchem.4c04391
摘要
Metal–organic frameworks (MOFs) are potential semiconductor materials, but they still face limitations, such as insufficient photoresponse, high recombination rates, and inadequate N2 adsorption/activation capabilities. Herein, a UiO-66-based system is designed via a natural chlorophyll sensitization strategy. Density functional theory calculations confirm the coordination interactions between chlorophyll and UiO-66. The chlorophyll-sensitized UiO-66 (Chlor@UiO-66) exhibits an improved NH3 production rate of 73.1 μmol g–1 h–1, compared to UiO-66 (6.3 μmol g–1 h–1). This enhancement is attributed to the dye properties of chlorophyll and the electron-donating effect of the structure, which broadens the visible light absorption range and facilitates charge carrier separation and transfer, as well as N2 adsorption/activation. In situ FT-IR characterization combined with theoretical calculations demonstrates that the reduction of N2 at the Chlor@UiO-66 surface follows the alternating hydrogenation pathway. This research provides new insights for the design and synthesis of novel natural chlorophyll-sensitized nanomaterials for the photocatalysis of small molecules.
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