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Molten salt synthesis of disordered spinel CoFe(2)O(4) with improved electrochemical performance for sodium-ion batteries
Sodium-ion (Na-ion) batteries are currently being investigated as an attractive substitute for lithium-ion (Li-ion) batteries in large energy storage systems because of the more abundant and less expensive supply of Na than Li. However, the reversible capacity of Na-ions is limited because Na posses...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664190/ https://www.ncbi.nlm.nih.gov/pubmed/38020019 http://dx.doi.org/10.1039/d3ra07050f |
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author | Muhamad, Sarah Umeera Idris, Nurul Hayati Yusoff, Hanis Mohd Md Din, Muhamad Faiz Majid, Siti Rohana Noerochim, Lukman |
author_facet | Muhamad, Sarah Umeera Idris, Nurul Hayati Yusoff, Hanis Mohd Md Din, Muhamad Faiz Majid, Siti Rohana Noerochim, Lukman |
author_sort | Muhamad, Sarah Umeera |
collection | PubMed |
description | Sodium-ion (Na-ion) batteries are currently being investigated as an attractive substitute for lithium-ion (Li-ion) batteries in large energy storage systems because of the more abundant and less expensive supply of Na than Li. However, the reversible capacity of Na-ions is limited because Na possesses a large ionic radius and has a higher standard electrode potential than that of Li, making it challenging to obtain electrode materials that are capable of storing large quantities of Na-ions. This study investigates the potential of CoFe(2)O(4) synthesised via the molten salt method as an anode for Na-ion batteries. The obtained phase structure, morphology and charge and discharge properties of CoFe(2)O(4) are thoroughly assessed. The synthesised CoFe(2)O(4) has an octahedron morphology, with a particle size in the range of 1.1–3.6 μm and a crystallite size of ∼26 nm. Moreover, the CoFe(2)O(4) (M800) electrodes can deliver a high discharge capacity of 839 mA h g(−1) in the first cycle at a current density of 0.1 A g(−1), reasonable cyclability of 98 mA h g(−1) after 100 cycles and coulombic efficiency of ∼99%. The improved electrochemical performances of CoFe(2)O(4) can be due to Na-ion-pathway shortening, wherein the homogeneity and small size of CoFe(2)O(4) particles may enhance the Na-ion transportation. Therefore, this simple synthetic approach using molten salt favours the Na-ion diffusion and electron transport to a great extent and maximises the utilisation of CoFe(2)O(4) as a potential anode material for Na-ion batteries. |
format | Online Article Text |
id | pubmed-10664190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-106641902023-11-22 Molten salt synthesis of disordered spinel CoFe(2)O(4) with improved electrochemical performance for sodium-ion batteries Muhamad, Sarah Umeera Idris, Nurul Hayati Yusoff, Hanis Mohd Md Din, Muhamad Faiz Majid, Siti Rohana Noerochim, Lukman RSC Adv Chemistry Sodium-ion (Na-ion) batteries are currently being investigated as an attractive substitute for lithium-ion (Li-ion) batteries in large energy storage systems because of the more abundant and less expensive supply of Na than Li. However, the reversible capacity of Na-ions is limited because Na possesses a large ionic radius and has a higher standard electrode potential than that of Li, making it challenging to obtain electrode materials that are capable of storing large quantities of Na-ions. This study investigates the potential of CoFe(2)O(4) synthesised via the molten salt method as an anode for Na-ion batteries. The obtained phase structure, morphology and charge and discharge properties of CoFe(2)O(4) are thoroughly assessed. The synthesised CoFe(2)O(4) has an octahedron morphology, with a particle size in the range of 1.1–3.6 μm and a crystallite size of ∼26 nm. Moreover, the CoFe(2)O(4) (M800) electrodes can deliver a high discharge capacity of 839 mA h g(−1) in the first cycle at a current density of 0.1 A g(−1), reasonable cyclability of 98 mA h g(−1) after 100 cycles and coulombic efficiency of ∼99%. The improved electrochemical performances of CoFe(2)O(4) can be due to Na-ion-pathway shortening, wherein the homogeneity and small size of CoFe(2)O(4) particles may enhance the Na-ion transportation. Therefore, this simple synthetic approach using molten salt favours the Na-ion diffusion and electron transport to a great extent and maximises the utilisation of CoFe(2)O(4) as a potential anode material for Na-ion batteries. The Royal Society of Chemistry 2023-11-22 /pmc/articles/PMC10664190/ /pubmed/38020019 http://dx.doi.org/10.1039/d3ra07050f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Muhamad, Sarah Umeera Idris, Nurul Hayati Yusoff, Hanis Mohd Md Din, Muhamad Faiz Majid, Siti Rohana Noerochim, Lukman Molten salt synthesis of disordered spinel CoFe(2)O(4) with improved electrochemical performance for sodium-ion batteries |
title | Molten salt synthesis of disordered spinel CoFe(2)O(4) with improved electrochemical performance for sodium-ion batteries |
title_full | Molten salt synthesis of disordered spinel CoFe(2)O(4) with improved electrochemical performance for sodium-ion batteries |
title_fullStr | Molten salt synthesis of disordered spinel CoFe(2)O(4) with improved electrochemical performance for sodium-ion batteries |
title_full_unstemmed | Molten salt synthesis of disordered spinel CoFe(2)O(4) with improved electrochemical performance for sodium-ion batteries |
title_short | Molten salt synthesis of disordered spinel CoFe(2)O(4) with improved electrochemical performance for sodium-ion batteries |
title_sort | molten salt synthesis of disordered spinel cofe(2)o(4) with improved electrochemical performance for sodium-ion batteries |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664190/ https://www.ncbi.nlm.nih.gov/pubmed/38020019 http://dx.doi.org/10.1039/d3ra07050f |
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