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Surfactant‐Mediated and Morphology‐Controlled Nanostructured LiFePO(4)/Carbon Composite as a Promising Cathode Material for Li‐Ion Batteries
The synthesis of morphology‐controlled carbon‐coated nanostructured LiFePO(4) (LFP/Carbon) cathode materials by surfactant‐assisted hydrothermal method using block copolymers is reported. The resulting nanocrystalline high surface area materials were coated with carbon and designated as LFP/C123 and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946950/ https://www.ncbi.nlm.nih.gov/pubmed/31921542 http://dx.doi.org/10.1002/open.201900175 |
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author | Khan, Sourav Raj, Rayappan Pavul George, Laurel Kannangara, G. S. Kamali Milev, Adriyan Varadaraju, Upadhyayula V. Selvam, Parasuraman |
author_facet | Khan, Sourav Raj, Rayappan Pavul George, Laurel Kannangara, G. S. Kamali Milev, Adriyan Varadaraju, Upadhyayula V. Selvam, Parasuraman |
author_sort | Khan, Sourav |
collection | PubMed |
description | The synthesis of morphology‐controlled carbon‐coated nanostructured LiFePO(4) (LFP/Carbon) cathode materials by surfactant‐assisted hydrothermal method using block copolymers is reported. The resulting nanocrystalline high surface area materials were coated with carbon and designated as LFP/C123 and LFP/C311. All the materials were systematically characterized by various analytical, spectroscopic and imaging techniques. The reverse structure of the surfactant Pluronic® 31R1 (PPO‐PEO‐PPO) in comparison to Pluronic® P123 (PEO‐PPO‐PEO) played a vital role in controlling the particle size and morphology which in turn ameliorate the electrochemical performance in terms of reversible specific capacity (163 mAh g(−1) and 140 mAh g(−1) at 0.1 C for LFP/C311 and LFP/C123, respectively). In addition, LFP/C311 demonstrated excellent electrochemical performance including lower charge transfer resistance (146.3 Ω) and excellent cycling stability (95 % capacity retention at 1 C after 100 cycles) and high rate capability (163.2 mAh g(−1) at 0.1 C; 147.1 mAh g(−1) at 1 C). The better performance of the former is attributed to LFP nanoparticles (<50 nm) with a specific spindle‐shaped morphology. Further, we have also evaluated the electrode performance with the use of both PVDF and CMC binders employed for the electrode fabrication. |
format | Online Article Text |
id | pubmed-6946950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69469502020-01-09 Surfactant‐Mediated and Morphology‐Controlled Nanostructured LiFePO(4)/Carbon Composite as a Promising Cathode Material for Li‐Ion Batteries Khan, Sourav Raj, Rayappan Pavul George, Laurel Kannangara, G. S. Kamali Milev, Adriyan Varadaraju, Upadhyayula V. Selvam, Parasuraman ChemistryOpen Full Papers The synthesis of morphology‐controlled carbon‐coated nanostructured LiFePO(4) (LFP/Carbon) cathode materials by surfactant‐assisted hydrothermal method using block copolymers is reported. The resulting nanocrystalline high surface area materials were coated with carbon and designated as LFP/C123 and LFP/C311. All the materials were systematically characterized by various analytical, spectroscopic and imaging techniques. The reverse structure of the surfactant Pluronic® 31R1 (PPO‐PEO‐PPO) in comparison to Pluronic® P123 (PEO‐PPO‐PEO) played a vital role in controlling the particle size and morphology which in turn ameliorate the electrochemical performance in terms of reversible specific capacity (163 mAh g(−1) and 140 mAh g(−1) at 0.1 C for LFP/C311 and LFP/C123, respectively). In addition, LFP/C311 demonstrated excellent electrochemical performance including lower charge transfer resistance (146.3 Ω) and excellent cycling stability (95 % capacity retention at 1 C after 100 cycles) and high rate capability (163.2 mAh g(−1) at 0.1 C; 147.1 mAh g(−1) at 1 C). The better performance of the former is attributed to LFP nanoparticles (<50 nm) with a specific spindle‐shaped morphology. Further, we have also evaluated the electrode performance with the use of both PVDF and CMC binders employed for the electrode fabrication. John Wiley and Sons Inc. 2019-09-27 /pmc/articles/PMC6946950/ /pubmed/31921542 http://dx.doi.org/10.1002/open.201900175 Text en ©2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Khan, Sourav Raj, Rayappan Pavul George, Laurel Kannangara, G. S. Kamali Milev, Adriyan Varadaraju, Upadhyayula V. Selvam, Parasuraman Surfactant‐Mediated and Morphology‐Controlled Nanostructured LiFePO(4)/Carbon Composite as a Promising Cathode Material for Li‐Ion Batteries |
title | Surfactant‐Mediated and Morphology‐Controlled Nanostructured LiFePO(4)/Carbon Composite as a Promising Cathode Material for Li‐Ion Batteries |
title_full | Surfactant‐Mediated and Morphology‐Controlled Nanostructured LiFePO(4)/Carbon Composite as a Promising Cathode Material for Li‐Ion Batteries |
title_fullStr | Surfactant‐Mediated and Morphology‐Controlled Nanostructured LiFePO(4)/Carbon Composite as a Promising Cathode Material for Li‐Ion Batteries |
title_full_unstemmed | Surfactant‐Mediated and Morphology‐Controlled Nanostructured LiFePO(4)/Carbon Composite as a Promising Cathode Material for Li‐Ion Batteries |
title_short | Surfactant‐Mediated and Morphology‐Controlled Nanostructured LiFePO(4)/Carbon Composite as a Promising Cathode Material for Li‐Ion Batteries |
title_sort | surfactant‐mediated and morphology‐controlled nanostructured lifepo(4)/carbon composite as a promising cathode material for li‐ion batteries |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946950/ https://www.ncbi.nlm.nih.gov/pubmed/31921542 http://dx.doi.org/10.1002/open.201900175 |
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