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组装用于高效电催化将CO还原为甲酸盐的金属有机层复合材料。

Assembling Metal Organic Layer Composites for High-Performance Electrocatalytic CO Reduction to Formate.

作者信息

Liu Hang, Wang Hongguang, Song Qian, Küster Kathrin, Starke Ulrich, van Aken Peter A, Klemm Elias

机构信息

Universität Stuttgart, Institut für Technische Chemie, Pfaffenwaldring 55, 70569, Stuttgart, Germany.

Max Planck Institute for Solid State Research, Heisenbergstraße 1, 70569, Stuttgart, Germany.

出版信息

Angew Chem Int Ed Engl. 2022 Feb 21;61(9):e202117058. doi: 10.1002/anie.202117058. Epub 2022 Jan 17.

Abstract

2D metal-organic-framework (MOF) based composites have emerged as promising candidates for electrocatalysis due to their high structural flexibility and fully exposed active sites. Herein, a freestanding metal-organic layer (MOL) with a 2D kgd (kagome dual) lattice was constructed with abundant surface oxygenate groups serving as anchoring sites to immobilize diverse guests. Taking Bi as an example, tetragonal Bi O nanowires can be uniformly grown on MOLs after solvothermal treatment, the structural evolution of which was followed by ex situ electron microscopy. The as-prepared Bi O /MOL exhibits excellent CO electroreduction activity towards formate reaching a specific current of 2.3 A mg and Faradaic efficiencies of over 85 % with a wide potential range from -0.87 to -1.17 V, far surpassing Bi O /UiO (a 3D Zr -oxo based MOF) and Bi O /AB (Acetylene Black). Such a post-synthetic modification strategy can be flexibly extended to develop versatile MOL composites, highlighting the superiority of optimizing MOL-based composites for electrocatalysis.

摘要

基于二维金属有机框架(MOF)的复合材料因其高结构灵活性和完全暴露的活性位点,已成为电催化领域有潜力的候选材料。在此,构建了一种具有二维kgd( Kagome对偶)晶格的独立金属有机层(MOL),其具有丰富的表面含氧基团作为锚定位点,用于固定各种客体。以Bi为例,经溶剂热处理后,四方相BiO纳米线可在MOL上均匀生长,通过非原位电子显微镜跟踪其结构演变。所制备的BiO/MOL对甲酸盐表现出优异的CO电还原活性,在-0.87至-1.17 V的宽电位范围内,特定电流达到2.3 A mg,法拉第效率超过85%,远远超过BiO/UiO(一种基于三维Zr-氧的MOF)和BiO/AB(乙炔黑)。这种合成后修饰策略可以灵活扩展,以开发多功能MOL复合材料,突出了优化基于MOL的复合材料用于电催化的优越性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fba6/9303648/08224524fce2/ANIE-61-0-g004.jpg

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