n -邻苯甲酰-γ-氨基丁酸-钴1D MOF†高效电催化水氧化

IF 2.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY New Journal of Chemistry Pub Date : 2024-12-05 DOI:10.1039/D4NJ03470H
Milan Gumtya, Ayan Mondal, Rahul Banerjee and Debasish Haldar
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引用次数: 0

摘要

水电解是生产氢气和氧气作为替代可再生燃料的关键。主要的挑战在于开发简单、经济、环保、过电位最小的催化剂。本研究介绍了一种钴基一维金属有机骨架(MOF)作为电化学条件下水氧化的高效催化剂。值得注意的是,Co(II)中心之间的配体和水桥在电催化中起着至关重要的作用。通过电化学、光谱学和电子显微镜分析,我们证明了1D MOF是一种有效的水氧化非均相电催化剂,法拉第效率高达85%,过电位仅为390 mV。这些发现为设计经济高效的过渡金属基水氧化催化剂提供了新的方向。
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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Efficient electrocatalytic water oxidation by N-phthaloyl-γ-aminobutyric acid-cobalt 1D MOF†

Water electrolysis is critical for generating hydrogen and oxygen as alternative renewable fuels. The primary challenge lies in developing simple, economical, and eco-friendly catalysts with minimal overpotential. This study introduces a cobalt-based 1D metal–organic framework (MOF) as a highly efficient catalyst for water oxidation under electrochemical conditions. Significantly, the ligand and water bridges between Co(II) centers play a crucial role in electrocatalysis. Through electrochemical, spectroscopic, and electron microscopy analyses, we demonstrate that the 1D MOF is an effective heterogeneous electrocatalyst for water oxidation, achieving a high faradaic efficiency of 85% and an overpotential of just 390 mV. These findings offer a new direction in designing cost-effective and highly efficient transition-metal-based catalysts for water oxidation.

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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
期刊最新文献
Back cover Back cover Development and validation of a high-throughput HPLC-MS/MS method for the simultaneous determination of exatecan and its cathepsin B-sensitive prodrug in rat plasma† A bimetallic catalyst of Fe–Co nanocomposite encapsulated in N-doped carbon nanotubes for colorimetric monitoring and degradation of hydroquinone in rivers† Impact of coordinated nitrogen atoms on the electrocatalytic water oxidation properties of copper complexes with pentadentate ligands†
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