材料科学
光催化
共价键
期限(时间)
生产(经济)
化学工程
纳米技术
催化作用
有机化学
化学
量子力学
物理
工程类
宏观经济学
经济
作者
Prasenjit Das,Gouri Chakraborty,Jin Yang,Jérôme Roeser,Hüseyin Küçükkeçeci,Nguyễn Anh Dũng,Michael Schwarze,José Gabriel,Christopher Penschke,Shengjun Du,Vincent Weigelt,Islam E. Khalil,Johannes Schmidt,Peter Saalfrank,Martin Oschatz,Jabor Rabeah,Reinhard Schomäcker,Franziska Emmerling,Arne Thomas
标识
DOI:10.1002/aenm.202501193
摘要
Abstract In nature, organic molecules play a vital role in light harvesting and photosynthesis. However, regarding artificial water splitting, the research focus is primarily on inorganic semiconductors. Although organic photocatalysts have high structural variability, they tend to exhibit lower quantum efficiencies for water splitting than their inorganic counterparts. Multicomponent reactions (MCRs) offer an attractive route to introduce different functional units into covalent organic frameworks (COFs) and enable semiconducting properties and high chemical stability, creating promising materials for long‐term photocatalytic applications, such as H 2 production. Herein, five highly crystalline donor‐acceptor based, 4‐substituted quinoline‐linked MCR‐COFs are presented that are prepared via the three‐component Povarov reaction. The pore functionality is varied by applying different vinyl derivatives (e.g., styrene, 2‐vinyl pyridine, 4‐vinylpyridine, 4‐vinyl imidazole, 2,3,4,5,6‐pentafluorostyrene), which has a strong influence on the obtained photocatalytic activity. Especially an imidazole‐functionalized COF displays promising photocatalytic performance due to its high surface area, crystallinity, and wettability. These properties enable it to maintain its photocatalytic activity even in a membrane support. Furthermore, such MCR‐COFs display dramatically enhanced (photo)chemical stability even after long‐term solar light irradiation and exhibit a high and steady H 2 evolution for at least 15 days.
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