Electrically Conductive Metal-organic Frameworks-Based Electrocatalysts: from synthesis strategies to catalytic applications

Abstract

Over the past decade, metal-organic frameworks (MOFs) have aroused significant interest as promising electrocatalysts for energy-related reactions. However, despite their potential, current research remains far from meeting commercial requirements due to inherent challenges, including limited electrical conductivity and low chemical stability. In this context, researchers are increasingly focusing on conductive metal-organic frameworks (c-MOFs) that exhibit a combination of efficient charge transport with high porosity, offering unprecedented properties for constructing highly active and stable electrocatalysts. Unfortunately, most c-MOF electrocatalysts struggle to achieve both industrial current density and long-term stability. This feature article aims to review a comprehensive overview of the recent progress in c-MOFs for various electrocatalysis applications. We briefly discuss the latest synthetic strategies for developing various c-MOFs, with dimensionality decreasing from three-dimensional (3D) frameworks to two-dimensional (2D) nanosheets. The focus then shifts to the efforts made thus far to clarify the relationship between chemical structures and charge transport mechanisms in c-MOFs. In addition, the utilization of several representative c-MOFs for electrocatalysis, focusing on HER, OER, NRR, and CO2RR are showcased, providing a brief overview of the reaction mechanisms and ongoing catalytic performance bottlenecks. Finally, some existing obstacles and prospects for constructing c-MOFs electrocatalysts with long-term stability are proposed.

Article information

Article type
Highlight
Submitted
01 Apr 2025
Accepted
05 Aug 2025
First published
07 Aug 2025

Chem. Commun., 2025, Accepted Manuscript

Electrically Conductive Metal-organic Frameworks-Based Electrocatalysts: from synthesis strategies to catalytic applications

N. Q. Tran, T. A. Le, N. D. Hai, T. T. N. Tran and K. T. L. Trinh, Chem. Commun., 2025, Accepted Manuscript , DOI: 10.1039/D5CC01825K

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