Multidentate Macrocyclic Salphen-Based 2D Conjugated Metal-Organic Framework.

IF 16.9
Pei Chen, Mingxuan Liu, Ruofan Li, Xi Su, Guolong Xing, Xiao-Rui Ren, Dong Wang, Jian Zhang, Long Chen
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Abstract

Two-dimensional conjugated metal-organic frameworks (2D c-MOFs) represent an emerging class of crystalline porous materials with promising electrochemical applications. The design of novel organic ligands for constructing 2D c-MOFs remains a crucial research frontier. While the incorporation of macrocycle blocks into 2D c-MOFs can introduce intrinsic cavities with advantageous properties, most existing reports are limited to coordinating with only one equivalent metal ion per macrocyclic cavity. In this work, we developed a triangular-shaped Salphen macrocycle-based 2D c-MOF (SM-MOF-Cu) featuring multidentate internal coordination sites. SM-MOF-Cu exhibits high crystallinity, permanent porosity, and abundant accessible metal sites. Remarkably, this material demonstrates exceptional performance in the electrocatalytic hydrogenation of acetylene to ethylene (E-HAE), achieving a Faradaic efficiency of 96.6% for ethylene production at -0.85 V versus the reversible hydrogen electrode (RHE) under continuous pure acetylene feed. This study not only broadens the family of macrocycle-based 2D c-MOFs but also provides new insights into their potential for advanced electrocatalysis.

Abstract Image

多齿大环沙芬基二维共轭金属有机骨架。
二维共轭金属有机框架(2D c-MOFs)是一类具有良好电化学应用前景的新型晶体多孔材料。设计新型有机配体构建二维c-MOFs是一个重要的研究前沿。虽然将大环块结合到二维c- mof中可以引入具有优势性质的固有腔,但大多数现有报道仅限于每个大环腔仅与一个等效金属离子配合。在这项工作中,我们开发了一种具有多齿内配位位点的三角形Salphen大环型二维c-MOF (SM-MOF-Cu)。SM-MOF-Cu具有高结晶度、永久孔隙和丰富的可接近金属位点。值得注意的是,该材料在乙炔电催化加氢制乙烯(E-HAE)方面表现出优异的性能,与连续纯乙炔进料的可逆氢电极(RHE)相比,在-0.85 V下,乙烯生产的法拉第效率达到96.6%。这项研究不仅拓宽了基于大环的2D c- mof家族,而且为其在高级电催化方面的潜力提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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