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DC Field | Value | Language |
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dc.contributor.author | Pandey, Jay | - |
dc.date.accessioned | 2025-07-22T06:49:56Z | - |
dc.date.available | 2025-07-22T06:49:56Z | - |
dc.date.issued | 2025-09 | - |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0254058425006017 | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/19048 | - |
dc.description.abstract | Developing 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.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.subject | Chemical engineering | en_US |
dc.subject | PEM fuel cell | en_US |
dc.subject | Electrocatalysts | en_US |
dc.subject | Carbon cloth | en_US |
dc.subject | Manganese oxide | en_US |
dc.title | In-situ growth of γ-Mn2O3 on activated carbon cloth for enhanced bifunctional electrocatalysis of ORR and OER | en_US |
dc.type | Article | en_US |
Appears in Collections: | Department of Chemical Engineering |
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