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基于羟基桥联双核铜(II)菲咯啉化合物的异质化分子电催化剂用于将CO选择性还原为乙烯

Heterogenized Molecular Electrocatalyst Based on a Hydroxo-Bridged Binuclear Copper(II) Phenanthroline Compound for Selective Reduction of CO to Ethylene.

作者信息

Liu Na, Bartling Stephan, Springer Armin, Kubis Christoph, Bokareva Olga S, Salaya Evaristo, Sun Jiameng, Zhang Zhonghua, Wohlrab Sebastian, Abdel-Mageed Ali M, Liang Hong-Qing, Francke Robert

机构信息

Leibniz Institute for Catalysis, Albert-Einstein-Str. 29a, 18059, Rostock, Germany.

Electron Microscopy Center, University Medicine Rostock, Strempelstr. 14, 18057, Rostock, Germany.

出版信息

Adv Mater. 2024 Feb;36(6):e2309526. doi: 10.1002/adma.202309526. Epub 2023 Dec 6.

DOI:10.1002/adma.202309526
PMID:37983740
Abstract

Molecular copper catalysts have emerged as promising candidates for the electrochemical reduction of CO . Notable features of such systems include the ability of Cu to generate C  products and the well-defined active sites that allow for targeted structural tuning. However, the frequently observed in situ formation of Cu nanoclusters has undermined the advantages of the molecular frameworks. It is therefore desirable to develop Cu-based catalysts that retain their molecular structures during electrolysis. In this context, a heterogenized binuclear hydroxo-bridged phenanthroline Cu(II) compound with a short Cu···Cu distance is reported as a simple yet efficient catalyst for electrogeneration of ethylene and other C products. In an aqueous electrolyte, the catalyst demonstrates remarkable performance, with excellent Faradaic efficiency for C products (62%) and minimal H evolution (8%). Furthermore, it exhibits high stability, manifested by no observable degradation during 15 h of continuous electrolysis. The preservation of the atomic distribution of the active sites throughout electrolysis is substantiated through comprehensive characterizations, including X-ray photoelectron and absorption spectroscopy, scanning and transmission electron microscopy, UV-vis spectroscopy, as well as control experiments. These findings establish a solid foundation for further investigations into targeted structural tuning, opening new avenues for enhancing the catalytic performance of Cu-based molecular electrocatalysts.

摘要

分子铜催化剂已成为电化学还原CO的有前景的候选者。这类体系的显著特点包括铜生成含碳产物的能力以及允许进行有针对性结构调整的明确活性位点。然而,经常观察到的铜纳米团簇的原位形成削弱了分子框架的优势。因此,开发在电解过程中保持其分子结构的铜基催化剂是很有必要的。在此背景下,报道了一种具有短Cu···Cu距离的异质双核羟基桥联菲咯啉铜(II)化合物,它是一种用于电化学生成乙烯和其他含碳产物的简单而高效的催化剂。在水性电解质中,该催化剂表现出卓越的性能,对含碳产物具有优异的法拉第效率(62%),析氢量极少(8%)。此外,它还表现出高稳定性,在连续电解15小时期间没有观察到降解现象。通过包括X射线光电子能谱和吸收光谱、扫描和透射电子显微镜、紫外可见光谱以及对照实验在内的全面表征,证实了整个电解过程中活性位点原子分布的保留。这些发现为进一步研究有针对性的结构调整奠定了坚实基础,为提高铜基分子电催化剂的催化性能开辟了新途径。

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