Suppr超能文献

混合配体功能化铀酰有机框架光催化产过氧化氢

Photocatalytic Hydrogen Peroxide Production by a Mixed Ligand-Functionalized Uranyl-Organic Framework.

作者信息

Wang Xuemin, Li Jinlu, Wei Xiaoyu, Song Jianxin, Xie Jian, Li Zhenyu, Yuan Mengnan, Jiang Lisha, Wang Yanlong, Liang Chao, Liu Wei

机构信息

School of Environmental and Material Engineering, Yantai University, Yantai 264005, Shandong, China.

Shandong Nuclear and Radiation Safety Monitoring Center, No. 145 Jingshi West Road, Jinan 250117, Shandong, China.

出版信息

ACS Omega. 2024 Jul 25;9(31):33671-33678. doi: 10.1021/acsomega.4c02181. eCollection 2024 Aug 6.

Abstract

Hydrogen peroxide (HO) production driven by solar energy has received enormous attention due to its high efficiency, low cost, and environmental friendliness characteristics. Searching for new photocatalytic materials for HO production is one of the most important targets. In this work, a new three-dimensional (3D) uranyl-organic framework material was constructed with mixed ligands via a solvothermal reaction and used for photocatalytic HO production. The mixed ligand strategy not only benefits the construction of a 3D uranyl-organic framework but also introduces strong photon absorption groups into the framework. The thiophene and pyridine rings in the framework enhance photon absorption and carrier transfer. In addition, with the assistance of the hydrogen abstraction reaction of uranyl centers, the HO production rate reaches 345 μmol h g. This study provides a new blueprint for exploring the artificial photosynthesis of HO through uranium-based metal-organic frameworks.

摘要

由于具有高效、低成本和环境友好的特性,由太阳能驱动的过氧化氢(HO)生产受到了广泛关注。寻找用于生产HO的新型光催化材料是最重要的目标之一。在这项工作中,通过溶剂热反应构建了一种新型的三维(3D)铀酰有机框架材料,并将其用于光催化生产HO。混合配体策略不仅有利于三维铀酰有机框架的构建,还将强光子吸收基团引入到框架中。框架中的噻吩和吡啶环增强了光子吸收和载流子转移。此外,在铀酰中心的氢提取反应的辅助下,HO的产率达到345 μmol h g。这项研究为通过铀基金属有机框架探索HO的人工光合作用提供了新的蓝图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adc9/11307301/9a03de1ba35a/ao4c02181_0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验