Two-Dimensional Conjugated Metal-Organic Frameworks for Electrocatalysis: Opportunities and Challenges.

ACS Nano

Center for Advancing Electronics Dresden (cfaed) and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Dresden, 01062, Germany.

Published: February 2022

AI Article Synopsis

  • 2D conjugated metal-organic frameworks (c-MOFs) are promising electrocatalysts for electrochemical energy conversion due to their unique structural and chemical properties.
  • Recent advances in their design and synthesis are vital for enhancing their effectiveness in various electrochemical reactions, like hydrogen evolution and carbon dioxide reduction.
  • This review highlights both the current successes and the ongoing challenges in optimizing 2D c-MOF electrocatalysts for better performance in energy conversion applications.

Article Abstract

A highly effective electrocatalyst is the central component of advanced electrochemical energy conversion. Recently, two-dimensional conjugated metal-organic frameworks (2D c-MOFs) have emerged as a class of promising electrocatalysts because of their advantages including 2D layered structure with high in-plane conjugation, intrinsic electrical conductivity, permanent pores, large surface area, chemical stability, and structural diversity. In this Review, we summarize the recent advances of 2D c-MOF electrocatalysts for electrochemical energy conversion. First, we introduce the chemical design principles and synthetic strategies of the reported 2D c-MOFs, as well as the functional design for the electrocatalysis. Subsequently, we present the representative 2D c-MOF electrocatalysts in various electrochemical reactions, such as hydrogen/oxygen evolution, and reduction reactions of oxygen, carbon dioxide, and nitrogen. We highlight the strategies for the structural design and property tuning of 2D c-MOF electrocatalysts to boost the catalytic performance, and we offer our perspectives in regard to the challenges to be overcome.

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Source
http://dx.doi.org/10.1021/acsnano.1c10544DOI Listing

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