Surface Reconstruction of Cobalt-Based Polyoxometalate and CNT Fiber Composite for Efficient Oxygen Evolution Reaction

Polyoxometalates (POMs), as carbon-free metal-oxo-clusters with unique structural properties, are emerging water-splitting electrocatalysts. Herein, we explore the development of cobalt-containing polyoxometalate immobilized over the carbon nanotube fiber (CNTF) (Co4POM@CNTF) towards efficient elect...

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Bibliographic Details
Published in:Catalysts Vol. 12; no. 10; p. 1242
Main Authors: Irsa Tariq, Muhammad Adeel Asghar, Abid Ali, Amin Badshah, Syed Mustansar Abbas, Waheed Iqbal, Muhammad Zubair, Ali Haider, Shahid Zaman
Format: Journal Article
Language:English
Published: MDPI AG 01-10-2022
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Summary:Polyoxometalates (POMs), as carbon-free metal-oxo-clusters with unique structural properties, are emerging water-splitting electrocatalysts. Herein, we explore the development of cobalt-containing polyoxometalate immobilized over the carbon nanotube fiber (CNTF) (Co4POM@CNTF) towards efficient electrochemical oxygen evolution reaction (OER). CNTF serves as an excellent electron mediator and highly conductive support, while the self-activation of the part of Co4POM through restructuring in basic media generates cobalt oxides and/or hydroxides that serve as catalytic sites for OER. A modified electrode fabricated through the drop-casting method followed by thermal treatment showed higher OER activity and enhanced stability in alkaline media. Furthermore, advanced physical characterization and electrochemical results demonstrate efficient charge transfer kinetics and high OER performance in terms of low overpotential, small Tafel slope, and good stability over an extended reaction time. The significantly high activity and stability achieved can be ascribed to the efficient electron transfer and highly electrochemically active surface area (ECSA) of the self-activated electrocatalyst immobilized over the highly conductive CNTF. This research is expected to pave the way for developing POM-based electrocatalysts for oxygen electrocatalysis.
ISSN:2073-4344
DOI:10.3390/catal12101242