MnO<sub>2</sub>-Templated CuBDC Metal Organic Framework: A Noble-Metal-Free Stable and Efficient pH-Universal Electrocatalyst for Oxygen Reduction Reaction

The development of noble-metal-free, efficient, cost-effective, and stable pH-universal electrocatalysts for the oxygen reduction reaction (ORR) is essential for enabling the widespread adoption of ORR-based fuel cells and batteries in practical applications. Herein, we report the design and fabrication of a MnO2-supported Cu-Metal Organic Framework (Cu-MOF) as a cost-effective, efficient, stable, and above all a pH-universal ORR electrocatalyst. Specifically, a simple and scalable synthetic approach for the templated synthesis of CuBDC MOF networks over presynthesized MnO2 nanosheets for the fabrication of CuBDC/MnO2 composite is presented. The so-crafted CuBDC/MnO2 composite well-characterized for its chemical, morphological, and electrochemical characteristics is demonstrated to be a pH-universal ORR electrocatalyst exhibiting excellent stability and electrocatalytic performance that is at par with that reported recently for the state-of-the-art noble metal-based ORR catalysts. The CuBDC/MnO2 composite exhibits a mass transfer limited four-electron pathway ORR at a potential of just 0.74 V versus the reversible hydrogen electrode (RHE), with an overpotential (ηORR) of 0.45 V under alkaline conditions. The as-fabricated electrocatalyst delivers a specific activity (current per unit area) of −4.58 ± 0.01 mA/cm2 and the mass activity (current per unit mass) of 8641.50 ± 0.01 mA/mgcat. Our detailed physicochemical and electrochemical investigations clearly establish that the unique synergism among the metal-oxide and MOF components in the CuBDC/MnO2 composite endows it with unique features that result in the abundant availability and redox accessibility of Cu-redox sites and easy mass transportation of oxygen across an electronically and ionically good conducting [CuBDC/MnO2]/electrolyte interface. The work presented herein signifies a significant advancement toward the development of cost-effective and sustainable ORR electrocatalysts, potentially paving the way for their widespread adoption in clean and affordable electrochemical technologies for storage and conversion of energy.

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Publication Details

Journal
ACS Applied Energy Materials
Published
2025-04-23
DOI
https://doi.org/10.1021/acsaem.4c03315
Citations
6
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
2.18

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article

MnO2-Templated CuBDC Metal Organic Framework: A Noble-Metal-Free Stable and Efficient pH-Universal Electrocatalyst for Oxygen Reduction Reaction

Sajad A. Bhat, Pravin P. Ingole, Mohsin Ahmad Bhat, Murtaza Manzoor Bhat et al.
6 citations
ACS Applied Energy Materials
Electrocatalysts for Energy Conversion
2.18
article

MnO2-Templated CuBDC Metal Organic Framework: A Noble-Metal-Free Stable and Efficient pH-Universal Electrocatalyst for Oxygen Reduction Reaction

Sajad A. Bhat, Pravin P. Ingole, Mohsin Ahmad Bhat, Murtaza Manzoor Bhat, Feroz Ahmad Sofi, Adil Amin Wani, Aamir Yaseen Bhat
article en
6 citations

Abstract

The development of noble-metal-free, efficient, cost-effective, and stable pH-universal electrocatalysts for the oxygen reduction reaction (ORR) is essential for enabling the widespread adoption of ORR-based fuel cells and batteries in practical applications. Herein, we report the design and fabrication of a MnO2-supported Cu-Metal Organic Framework (Cu-MOF) as a cost-effective, efficient, stable, and above all a pH-universal ORR electrocatalyst. Specifically, a simple and scalable synthetic approach for the templated synthesis of CuBDC MOF networks over presynthesized MnO2 nanosheets for the fabrication of CuBDC/MnO2 composite is presented. The so-crafted CuBDC/MnO2 composite well-characterized for its chemical, morphological, and electrochemical characteristics is demonstrated to be a pH-universal ORR electrocatalyst exhibiting excellent stability and electrocatalytic performance that is at par with that reported recently for the state-of-the-art noble metal-based ORR catalysts. The CuBDC/MnO2 composite exhibits a mass transfer limited four-electron pathway ORR at a potential of just 0.74 V versus the reversible hydrogen electrode (RHE), with an overpotential (ηORR) of 0.45 V under alkaline conditions. The as-fabricated electrocatalyst delivers a specific activity (current per unit area) of −4.58 ± 0.01 mA/cm2 and the mass activity (current per unit mass) of 8641.50 ± 0.01 mA/mgcat. Our detailed physicochemical and electrochemical investigations clearly establish that the unique synergism among the metal-oxide and MOF components in the CuBDC/MnO2 composite endows it with unique features that result in the abundant availability and redox accessibility of Cu-redox sites and easy mass transportation of oxygen across an electronically and ionically good conducting [CuBDC/MnO2]/electrolyte interface. The work presented herein signifies a significant advancement toward the development of cost-effective and sustainable ORR electrocatalysts, potentially paving the way for their widespread adoption in clean and affordable electrochemical technologies for storage and conversion of energy.

ACS Applied Energy MaterialsVol. 8(9)
University of Kashmir (IN), University of Moratuwa (LK), Indian Institute of Technology Delhi (IN)
Science and Engineering Research Board
Clean water and sanitation
Openalex Percentile: Top 13%
Electrocatalysts for Energy Conversion
2.18
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