MOF-Based Dual-Layer Pickering Emulsion: Molecular-Level Gating of Water Delivery at Water-Oil Interface for Efficient Photocatalytic Hydrogenation Using H2O as a Hydrogen Source

IF 16.9 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Angewandte Chemie International Edition Pub Date : 2025-01-02 DOI:10.1002/anie.202421341
Prof. Dr. Kuo Yuan, Ying Zhang, Dr. Zhuang Yan, Prof. Dr. Qinbai Yun, Dr. Tianqun Song, Prof. Dr. Jun Guo, Jie Feng, Dr. Zheng Chen, Prof. Dr. Xiaotao Zhang, Prof. Dr. Zhiyong Tang, Prof. Dr. Wenping Hu, Prof. Dr. Tongbu Lu
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Abstract

Biphasic system not only presents a promising opportunity for complex catalytic processes, but also is a grand challenge in efficient tandem reactions. As an emerging solar-to-chemical conversion, the visible-light-driven and water-donating hydrogenation combines the sustainability of photocatalysis and economic-value of hydrogenation. However, the key and challenging point is to couple water-soluble photocatalytic hydrogen evolution reaction (HER) with oil-soluble hydrogenation. Herein, we employed metal–organic frameworks (MOFs) and CdS nanorods to construct a MOF-CdS dual-layer Pickering emulsion (water in oil, W/O), which compartmented aqueous phase for photocatalytic HER and oil phase for hydrogenation. The hydrophobic MOF and hydrophilic CdS were isolated at the inner and outer layers of W/O emulsion, respectively. The molecularly regulated hydrophobicity of MOF controlled the water delivery onto CdS photocatalysts, which realized the synergistic regulation of HER and hydrogenation. In the photocatalytic hydrogenation of cinnamaldehyde, the highest yield of MOF-CdS Pickering emulsion reached 187.37 mmol ⋅ g−1 ⋅ h−1, 30 times that of the counterpart without emulsion (6.44 mmol ⋅ g−1 ⋅ h−1). Its apparent quantum yield reached 43.24 % without co-catalysts. To our knowledge, this performance is at a top-level so far. Our work realized the precise regulation of water-oil interface to effectively couple two reactions in different phases, providing new perspective for challenging tandem catalysis.

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基于mof的双层酸洗乳液:水-油界面水输送的分子水平门控,以H2O为氢源进行高效光催化加氢
双相体系不仅为复杂的催化过程提供了良好的机会,而且对高效的串联反应提出了巨大的挑战。作为一种新兴的太阳能-化学转化技术,可见光驱动和供水加氢结合了光催化的可持续性和加氢的经济价值。然而,将水溶性光催化析氢反应(HER)与油溶性加氢反应(oil-soluble hydrogenation)结合起来是关键和难点。本文采用金属有机框架(mof)和CdS纳米棒构建了MOF-CdS双层Pickering乳剂(油中水,W/O),将水相分离用于光催化HER,油相分离用于加氢。在水乳状液的内层和外层分别分离到疏水性MOF和亲水性CdS。分子调控MOF的疏水性控制了CdS光催化剂上的水传递,实现了HER和加氢的协同调控。在肉桂醛的光催化加氢反应中,MOF-CdS Pickering乳液的产率最高可达187.37 mmol·g-1·h-1,是未加乳液的MOF-CdS Pickering乳液产率(6.44 mmol·g-1·h-1)的30倍。在无助催化剂的情况下,表观量子产率达到43.24%。据我们所知,这是迄今为止最高水平的表现。我们的工作实现了水-油界面的精确调控,有效地耦合了两个不同相的反应,为具有挑战性的串联催化提供了新的视角。
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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
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