JOURNAL ARTICLE

Ultrathin 2D Cobalt Zeolite‐Imidazole Framework Nanosheets for Electrocatalytic Oxygen Evolution

Abstract

Abstract 2D layered materials, including metal‐di‐chalcogenides and transition metal layered double hydroxides, among others, are intensively studied because of new properties that emerge from their 2D confinement, which are attractive for advanced applications. Herein, 2D cobalt ion (Co 2+ ) and benzimidazole (bIm) based zeolite‐imidazole framework nanosheets, ZIF‐9(III), are reported as exceptionally efficient electrocatalysts for the oxygen evolution reaction (OER). Specifically, liquid‐phase ultrasonication is applied to exfoliate a [Co 4 (bIm) 16 ] zeolite‐imidazole framework (ZIF), named as ZIF‐9(III) phase, into nanoscale sheets. ZIF‐9(III) is selectively prepared through simple mechanical grinding of cobalt nitrate and benzimidazole in the presence of a small amount of ethanol. The resultant exfoliated nanosheets exhibit significantly higher OER activity in alkaline conditions than the corresponding bulk phases ZIF‐9 and ZIF‐9(III). The electrochemical and physicochemical characterization data support the assignment of the OER activity of the exfoliated nanosheet derived material to nitrogen coordinated cobalt oxyhydroxide N 4 CoOOH sites, following a mechanism known for Co‐porphyrin and related systems. Thus, exfoliated 2D nanosheets hold promise as potential alternatives to commercial noble metal electrocatalysts for the OER.

Keywords:
Oxygen evolution Nanosheet Cobalt Materials science Zeolite Chemical engineering Electrochemistry Electrocatalyst Catalysis Inorganic chemistry Nanotechnology Chemistry Electrode Organic chemistry Metallurgy

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Citation History

Topics

Electrocatalysts for Energy Conversion
Physical Sciences →  Energy →  Renewable Energy, Sustainability and the Environment
Electrochemical Analysis and Applications
Physical Sciences →  Chemistry →  Electrochemistry
Fuel Cells and Related Materials
Physical Sciences →  Engineering →  Electrical and Electronic Engineering

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