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Nanostructured Silicon–Carbon 3D Electrode Architectures for High-Performance Lithium-Ion Batteries
[Image: see text] Silicon is an attractive anode material for lithium-ion batteries. However, silicon anodes have the issue of volume change, which causes pulverization and subsequently rapid capacity fade. Herein, we report organic binder and conducting diluent-free silicon–carbon 3D electrodes as...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644623/ https://www.ncbi.nlm.nih.gov/pubmed/31459090 http://dx.doi.org/10.1021/acsomega.8b00924 |
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author | Kumar, Sarode Krishna Ghosh, Sourav Malladi, Sairam K. Nanda, Jagjit Martha, Surendra K. |
author_facet | Kumar, Sarode Krishna Ghosh, Sourav Malladi, Sairam K. Nanda, Jagjit Martha, Surendra K. |
author_sort | Kumar, Sarode Krishna |
collection | PubMed |
description | [Image: see text] Silicon is an attractive anode material for lithium-ion batteries. However, silicon anodes have the issue of volume change, which causes pulverization and subsequently rapid capacity fade. Herein, we report organic binder and conducting diluent-free silicon–carbon 3D electrodes as anodes for lithium-ion batteries, where we replace the conventional copper (Cu) foil current collector with highly conductive carbon fibers (CFs) of 5–10 μm in diameter. We demonstrate here the petroleum pitch (P-pitch) which adequately coat between the CFs and Si-nanoparticles (NPs) between 700 and 1000 °C under argon atmosphere and forms uniform continuous layer of 6–14 nm thick coating along the exterior surfaces of Si-NPs and 3D CFs. The electrodes fabricate at 1000 °C deliver capacities in excess of 2000 mA h g(–1) at C/10 and about 1000 mA h g(–1) at 5 C rate for 250 cycles in half-cell configuration. Synergistic effect of carbon coating and 3D CF electrode architecture at 1000 °C improve the efficiency of the Si–C composite during long cycling. Full cells using Si–carbon composite electrode and Li(1.2)Ni(0.15)Mn(0.55)Co(0.1)O(2-)based cathode show high open-circuit voltage of >4 V and energy density of >500 W h kg(–1). Replacement of organic binder and copper current collector by high-temperature binder P-pitch and CFs further enhances energy density per unit area of the electrode. It is believed that the study will open a new realm of possibility for the development of Li-ion cell having almost double the energy density of currently available Li-ion batteries that is suitable for electric vehicles. |
format | Online Article Text |
id | pubmed-6644623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66446232019-08-27 Nanostructured Silicon–Carbon 3D Electrode Architectures for High-Performance Lithium-Ion Batteries Kumar, Sarode Krishna Ghosh, Sourav Malladi, Sairam K. Nanda, Jagjit Martha, Surendra K. ACS Omega [Image: see text] Silicon is an attractive anode material for lithium-ion batteries. However, silicon anodes have the issue of volume change, which causes pulverization and subsequently rapid capacity fade. Herein, we report organic binder and conducting diluent-free silicon–carbon 3D electrodes as anodes for lithium-ion batteries, where we replace the conventional copper (Cu) foil current collector with highly conductive carbon fibers (CFs) of 5–10 μm in diameter. We demonstrate here the petroleum pitch (P-pitch) which adequately coat between the CFs and Si-nanoparticles (NPs) between 700 and 1000 °C under argon atmosphere and forms uniform continuous layer of 6–14 nm thick coating along the exterior surfaces of Si-NPs and 3D CFs. The electrodes fabricate at 1000 °C deliver capacities in excess of 2000 mA h g(–1) at C/10 and about 1000 mA h g(–1) at 5 C rate for 250 cycles in half-cell configuration. Synergistic effect of carbon coating and 3D CF electrode architecture at 1000 °C improve the efficiency of the Si–C composite during long cycling. Full cells using Si–carbon composite electrode and Li(1.2)Ni(0.15)Mn(0.55)Co(0.1)O(2-)based cathode show high open-circuit voltage of >4 V and energy density of >500 W h kg(–1). Replacement of organic binder and copper current collector by high-temperature binder P-pitch and CFs further enhances energy density per unit area of the electrode. It is believed that the study will open a new realm of possibility for the development of Li-ion cell having almost double the energy density of currently available Li-ion batteries that is suitable for electric vehicles. American Chemical Society 2018-08-21 /pmc/articles/PMC6644623/ /pubmed/31459090 http://dx.doi.org/10.1021/acsomega.8b00924 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Kumar, Sarode Krishna Ghosh, Sourav Malladi, Sairam K. Nanda, Jagjit Martha, Surendra K. Nanostructured Silicon–Carbon 3D Electrode Architectures for High-Performance Lithium-Ion Batteries |
title | Nanostructured Silicon–Carbon 3D Electrode
Architectures for High-Performance Lithium-Ion Batteries |
title_full | Nanostructured Silicon–Carbon 3D Electrode
Architectures for High-Performance Lithium-Ion Batteries |
title_fullStr | Nanostructured Silicon–Carbon 3D Electrode
Architectures for High-Performance Lithium-Ion Batteries |
title_full_unstemmed | Nanostructured Silicon–Carbon 3D Electrode
Architectures for High-Performance Lithium-Ion Batteries |
title_short | Nanostructured Silicon–Carbon 3D Electrode
Architectures for High-Performance Lithium-Ion Batteries |
title_sort | nanostructured silicon–carbon 3d electrode
architectures for high-performance lithium-ion batteries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644623/ https://www.ncbi.nlm.nih.gov/pubmed/31459090 http://dx.doi.org/10.1021/acsomega.8b00924 |
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