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Artificial solid electrolyte interphase for aqueous lithium energy storage systems
Aqueous lithium energy storage systems address environmental sustainability and safety issues. However, significant capacity fading after repeated cycles of charge-discharge and during float charge limit their practical application compared to their nonaqueous counterparts. We introduce an artificia...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590782/ https://www.ncbi.nlm.nih.gov/pubmed/28913426 http://dx.doi.org/10.1126/sciadv.1701010 |
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author | Zhi, Jian Yazdi, Alireza Zehtab Valappil, Gayathri Haime, Jessica Chen, Pu |
author_facet | Zhi, Jian Yazdi, Alireza Zehtab Valappil, Gayathri Haime, Jessica Chen, Pu |
author_sort | Zhi, Jian |
collection | PubMed |
description | Aqueous lithium energy storage systems address environmental sustainability and safety issues. However, significant capacity fading after repeated cycles of charge-discharge and during float charge limit their practical application compared to their nonaqueous counterparts. We introduce an artificial solid electrolyte interphase (SEI) to the aqueous systems and report the use of graphene films as an artificial SEI (G-SEI) that substantially enhance the overall performance of an aqueous lithium battery and a supercapacitor. The thickness (1 to 50 nm) and the surface area (1 cm(2) to 1 m(2)) of the G-SEI are precisely controlled on the LiMn(2)O(4)-based cathode using the Langmuir trough–based techniques. The aqueous battery with a 10-nm-thick G-SEI exhibits a discharge capacity as high as 104 mA·hour g(−1) after 600 cycles and a float charge current density as low as 1.03 mA g(−1) after 1 day, 26% higher (74 mA·hour g(−1)) and 54% lower (1.88 mA g(−1)) than the battery without the G-SEI, respectively. We propose that the G-SEI on the cathode surface simultaneously suppress the structural distortion of the LiMn(2)O(4) (the Jahn-Teller distortion) and the oxidation of conductive carbon through controlled diffusion of Li(+) and restricted permeation of gases (O(2) and CO(x)), respectively. The G-SEI on both small (~1 cm(2) in 1.15 mA·hour cell) and large (~9 cm(2) in 7 mA·hour cell) cathodes exhibit similar property enhancement, demonstrating excellent potential for scale-up and manufacturing. |
format | Online Article Text |
id | pubmed-5590782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55907822017-09-14 Artificial solid electrolyte interphase for aqueous lithium energy storage systems Zhi, Jian Yazdi, Alireza Zehtab Valappil, Gayathri Haime, Jessica Chen, Pu Sci Adv Research Articles Aqueous lithium energy storage systems address environmental sustainability and safety issues. However, significant capacity fading after repeated cycles of charge-discharge and during float charge limit their practical application compared to their nonaqueous counterparts. We introduce an artificial solid electrolyte interphase (SEI) to the aqueous systems and report the use of graphene films as an artificial SEI (G-SEI) that substantially enhance the overall performance of an aqueous lithium battery and a supercapacitor. The thickness (1 to 50 nm) and the surface area (1 cm(2) to 1 m(2)) of the G-SEI are precisely controlled on the LiMn(2)O(4)-based cathode using the Langmuir trough–based techniques. The aqueous battery with a 10-nm-thick G-SEI exhibits a discharge capacity as high as 104 mA·hour g(−1) after 600 cycles and a float charge current density as low as 1.03 mA g(−1) after 1 day, 26% higher (74 mA·hour g(−1)) and 54% lower (1.88 mA g(−1)) than the battery without the G-SEI, respectively. We propose that the G-SEI on the cathode surface simultaneously suppress the structural distortion of the LiMn(2)O(4) (the Jahn-Teller distortion) and the oxidation of conductive carbon through controlled diffusion of Li(+) and restricted permeation of gases (O(2) and CO(x)), respectively. The G-SEI on both small (~1 cm(2) in 1.15 mA·hour cell) and large (~9 cm(2) in 7 mA·hour cell) cathodes exhibit similar property enhancement, demonstrating excellent potential for scale-up and manufacturing. American Association for the Advancement of Science 2017-09-08 /pmc/articles/PMC5590782/ /pubmed/28913426 http://dx.doi.org/10.1126/sciadv.1701010 Text en Copyright © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Zhi, Jian Yazdi, Alireza Zehtab Valappil, Gayathri Haime, Jessica Chen, Pu Artificial solid electrolyte interphase for aqueous lithium energy storage systems |
title | Artificial solid electrolyte interphase for aqueous lithium energy storage systems |
title_full | Artificial solid electrolyte interphase for aqueous lithium energy storage systems |
title_fullStr | Artificial solid electrolyte interphase for aqueous lithium energy storage systems |
title_full_unstemmed | Artificial solid electrolyte interphase for aqueous lithium energy storage systems |
title_short | Artificial solid electrolyte interphase for aqueous lithium energy storage systems |
title_sort | artificial solid electrolyte interphase for aqueous lithium energy storage systems |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590782/ https://www.ncbi.nlm.nih.gov/pubmed/28913426 http://dx.doi.org/10.1126/sciadv.1701010 |
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