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Carbon nanoparticle-entrapped macroporous Mn(3)O(4) microsphere anodes with improved cycling stability for Li-ion batteries

Manganese oxide (Mn(3)O(4)) has garnered substantial attention as a low-cost, environment-friendly anode material. It undergoes a conversion reaction involving the formation of Li(2)O and metallic Mn to provide high-energy Li-ion batteries. However, its low electrical conductivity and significant vo...

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Autores principales: Kozawa, Takahiro, Kitabayashi, Fumiya, Fukuyama, Kayo, Naito, Makio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283411/
https://www.ncbi.nlm.nih.gov/pubmed/35835846
http://dx.doi.org/10.1038/s41598-022-16383-0
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author Kozawa, Takahiro
Kitabayashi, Fumiya
Fukuyama, Kayo
Naito, Makio
author_facet Kozawa, Takahiro
Kitabayashi, Fumiya
Fukuyama, Kayo
Naito, Makio
author_sort Kozawa, Takahiro
collection PubMed
description Manganese oxide (Mn(3)O(4)) has garnered substantial attention as a low-cost, environment-friendly anode material. It undergoes a conversion reaction involving the formation of Li(2)O and metallic Mn to provide high-energy Li-ion batteries. However, its low electrical conductivity and significant volume change reduce its capacity during the initial lithiation/delithiation, hindering its practical application. To improve the cycle performance, we propose a new composite structure wherein we entrap carbon nanoparticles in macroporous Mn(3)O(4) microspheres with a unique maze-like porous interior. We fabricate the Mn(3)O(4)/C composites using a scalable two-step process involving the thermal decomposition of MnCO(3) in water vapor and mixing in a carbon-dispersed solution. The fabricated Mn(3)O(4)/C composites with varying carbon contents exhibit a high maximum discharge capacity retention of 86% after 50 cycles, compared to the 18% given by bare Mn(3)O(4). The entrapped carbon nanoparticles improve the cycle performance both electrochemically and physically. The microstructure of the composite particles and the fabrication process developed in this study will help improve the performance of other conversion-type anode materials that suffer from cycle degradation, including inexpensive transition metal oxides and sulfides.
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spelling pubmed-92834112022-07-16 Carbon nanoparticle-entrapped macroporous Mn(3)O(4) microsphere anodes with improved cycling stability for Li-ion batteries Kozawa, Takahiro Kitabayashi, Fumiya Fukuyama, Kayo Naito, Makio Sci Rep Article Manganese oxide (Mn(3)O(4)) has garnered substantial attention as a low-cost, environment-friendly anode material. It undergoes a conversion reaction involving the formation of Li(2)O and metallic Mn to provide high-energy Li-ion batteries. However, its low electrical conductivity and significant volume change reduce its capacity during the initial lithiation/delithiation, hindering its practical application. To improve the cycle performance, we propose a new composite structure wherein we entrap carbon nanoparticles in macroporous Mn(3)O(4) microspheres with a unique maze-like porous interior. We fabricate the Mn(3)O(4)/C composites using a scalable two-step process involving the thermal decomposition of MnCO(3) in water vapor and mixing in a carbon-dispersed solution. The fabricated Mn(3)O(4)/C composites with varying carbon contents exhibit a high maximum discharge capacity retention of 86% after 50 cycles, compared to the 18% given by bare Mn(3)O(4). The entrapped carbon nanoparticles improve the cycle performance both electrochemically and physically. The microstructure of the composite particles and the fabrication process developed in this study will help improve the performance of other conversion-type anode materials that suffer from cycle degradation, including inexpensive transition metal oxides and sulfides. Nature Publishing Group UK 2022-07-14 /pmc/articles/PMC9283411/ /pubmed/35835846 http://dx.doi.org/10.1038/s41598-022-16383-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kozawa, Takahiro
Kitabayashi, Fumiya
Fukuyama, Kayo
Naito, Makio
Carbon nanoparticle-entrapped macroporous Mn(3)O(4) microsphere anodes with improved cycling stability for Li-ion batteries
title Carbon nanoparticle-entrapped macroporous Mn(3)O(4) microsphere anodes with improved cycling stability for Li-ion batteries
title_full Carbon nanoparticle-entrapped macroporous Mn(3)O(4) microsphere anodes with improved cycling stability for Li-ion batteries
title_fullStr Carbon nanoparticle-entrapped macroporous Mn(3)O(4) microsphere anodes with improved cycling stability for Li-ion batteries
title_full_unstemmed Carbon nanoparticle-entrapped macroporous Mn(3)O(4) microsphere anodes with improved cycling stability for Li-ion batteries
title_short Carbon nanoparticle-entrapped macroporous Mn(3)O(4) microsphere anodes with improved cycling stability for Li-ion batteries
title_sort carbon nanoparticle-entrapped macroporous mn(3)o(4) microsphere anodes with improved cycling stability for li-ion batteries
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283411/
https://www.ncbi.nlm.nih.gov/pubmed/35835846
http://dx.doi.org/10.1038/s41598-022-16383-0
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