光电流
人工光合作用
分解水
合理设计
三吡啶
催化作用
材料科学
金属有机骨架
光催化
纳米技术
光催化分解水
金属
化学工程
化学
光电子学
有机化学
工程类
吸附
冶金
作者
Jully Patel,Gabriel Bury,Yulia Pushkar
出处
期刊:Small
[Wiley]
日期:2024-05-15
卷期号:20 (37): e2310106-e2310106
被引量:18
标识
DOI:10.1002/smll.202310106
摘要
Abstract Metal‐Organic Frameworks (MOFs) recently emerged as a new platform for the realization of integrated devices for artificial photosynthesis. However, there remain few demonstrations of rational tuning of such devices for improved performance. Here, a fast molecular water oxidation catalyst working via water nucleophilic attack is integrated into the MOF MIL‐142, wherein Fe 3 O nodes absorb visible light, leading to charge separation. Materials are characterized by a range of structural and spectroscopic techniques. New, [Ru(tpy)(Qc)(H 2 O)] + (tpy = 2,2′:6′,2″‐terpyridine and Qc = 8‐quinolinecarboxylate)‐doped Fe MIL‐142 achieved a high photocurrent (1.6 × 10 −3 A·cm −2 ) in photo‐electrocatalytic water splitting at pH = 1. Unassisted photocatalytic H 2 evolution is also reported with Pt as the co‐catalyst (4.8 µmol g −1 min −1 ). The high activity of this new system enables hydrogen gas capture from an easy‐to‐manufacture, scaled‐up prototype utilizing MOF deposited on FTO glass as a photoanode. These findings provide insights for the development of MOF‐based light‐driven water‐splitting assemblies utilizing a minimal amount of precious metals and Fe‐based photosensitizers.
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