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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/19048
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dc.contributor.authorPandey, Jay-
dc.date.accessioned2025-07-22T06:49:56Z-
dc.date.available2025-07-22T06:49:56Z-
dc.date.issued2025-09-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0254058425006017-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/19048-
dc.description.abstractDeveloping cost-effective and high-performance electrocatalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is critical for advancements in metal-air batteries, proton exchange membrane PEM fuel cells, and water-splitting systems. These systems require highly active and stable electrocatalysts to enhance the ORR and OER performance to increase the device's efficiency. Herein, we report the synthesis of γ-Mn2O3 nanoparticles doped onto activated carbon cloth (A-CC) (γ-Mn2O3/A-CC) via simple and scalable hydrothermal process followed by annealing. This work investigates the potential of γ-Mn2O3/A-CC as a bifunctional electrocatalyst for ORR and OER in alkaline media. In ORR condition, the γ-Mn2O3/A-CC electrocatalyst exhibited half-wave potential (E1/2) of 0.708 V, while in OER, the electrocatalyst exhibited overpotential of 522 mV at 10 mA cm−2 and low Tafel slope of 40.6 mV dec−1. The electrochemical performance of the synthesized catalysts is comparable to the state-of-the-art Pt/C and RuO2/C electrocatalysts. This study provides a comprehensive understanding of the electrocatalytic activity of γ-Mn2O3/A-CC, highlighting its potential application in advanced energy conversion devices.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectChemical engineeringen_US
dc.subjectPEM fuel cellen_US
dc.subjectElectrocatalystsen_US
dc.subjectCarbon clothen_US
dc.subjectManganese oxideen_US
dc.titleIn-situ growth of γ-Mn2O3 on activated carbon cloth for enhanced bifunctional electrocatalysis of ORR and OERen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemical Engineering

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