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Title: | Unraveling the Synergistic Role of Sm3+ Doped NiFe-LDH as High-Performance Electrocatalysts for Improved Anion Exchange Membrane and Water Splitting Applications |
Authors: | Minhas, Harpriya Pathak, Biswarup |
Keywords: | anion exchange membrane (AEM) water electrolysis;Density Functional Theory (DFT);electrocatalytic water splitting;layered double hydroxides (LDHs);overpotentials;stability |
Issue Date: | 2024 |
Publisher: | John Wiley and Sons Inc |
Citation: | Nagappan, S., Gurusamy, H., Minhas, H., Karmakar, A., Ravichandran, S., Pathak, B., & Kundu, S. (2024). Unraveling the Synergistic Role of Sm3+ Doped NiFe-LDH as High-Performance Electrocatalysts for Improved Anion Exchange Membrane and Water Splitting Applications. Small Methods. Scopus. https://doi.org/10.1002/smtd.202401655 |
Abstract: | Effective first-row transition metal-based electrocatalysts are crucial for large-scale hydrogen energy generation and anion exchange membrane (AEM) devices in water splitting. The present work describes that SmNi0.02Fe-LDH nanosheets on nickel foam are used as a bifunctional electrocatalyst for water splitting and AEM water electrolyzer study. Tuning the Ni-to-Fe ratios in NiFe-LDH and doping with Sm ions improves the electrical structure and intrinsic activity. SmNi0.02Fe-LDH has higher oxygen evolution reaction (OER), HER, and TWS activity, achieving 10 mA cm⁻2 current density at lower overpotentials (230 mV, 95 mV, and 1.62 V, respectively). In AEMWE cells, SmNi0.02Fe-LDH as a cathode and anode pair exhibits outstanding activity (0.9 A cm⁻2 at 2 V) and stability over 120 h. Density Functional Theory (DFT) investigations reveal that the Sm doping in NiFe-LDH surface enhances its bifunctional activity toward OER and HER. These findings emphasize the potential of non-noble composites for long-term water electrolysis in total water splitting and AEMWE applications. © 2024 Wiley-VCH GmbH. |
URI: | https://doi.org/10.1002/smtd.202401655 https://dspace.iiti.ac.in/handle/123456789/15179 |
ISSN: | 2366-9608 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Chemistry |
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