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Li, Na, K, Mg, Zn, Al, and Ca Anode Interface Chemistries Developed by Solid‐State Electrolytes

Solid‐state batteries (SSBs) have received significant attention due to their high energy density, reversible cycle life, and safe operations relative to commercial Li‐ion batteries using flammable liquid electrolytes. This review presents the fundamentals, structures, thermodynamics, chemistries, a...

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Autores principales: Shinde, Sambhaji S., Wagh, Nayantara K., Kim, Sung‐Hae, Lee, Jung‐Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646287/
https://www.ncbi.nlm.nih.gov/pubmed/37743719
http://dx.doi.org/10.1002/advs.202304235
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author Shinde, Sambhaji S.
Wagh, Nayantara K.
Kim, Sung‐Hae
Lee, Jung‐Ho
author_facet Shinde, Sambhaji S.
Wagh, Nayantara K.
Kim, Sung‐Hae
Lee, Jung‐Ho
author_sort Shinde, Sambhaji S.
collection PubMed
description Solid‐state batteries (SSBs) have received significant attention due to their high energy density, reversible cycle life, and safe operations relative to commercial Li‐ion batteries using flammable liquid electrolytes. This review presents the fundamentals, structures, thermodynamics, chemistries, and electrochemical kinetics of desirable solid electrolyte interphase (SEI) required to meet the practical requirements of reversible anodes. Theoretical and experimental insights for metal nucleation, deposition, and stripping for the reversible cycling of metal anodes are provided. Ion transport mechanisms and state‐of‐the‐art solid‐state electrolytes (SEs) are discussed for realizing high‐performance cells. The interface challenges and strategies are also concerned with the integration of SEs, anodes, and cathodes for large‐scale SSBs in terms of physical/chemical contacts, space‐charge layer, interdiffusion, lattice‐mismatch, dendritic growth, chemical reactivity of SEI, current collectors, and thermal instability. The recent innovations for anode interface chemistries developed by SEs are highlighted with monovalent (lithium (Li(+)), sodium (Na(+)), potassium (K(+))) and multivalent (magnesium (Mg(2+)), zinc (Zn(2+)), aluminum (Al(3+)), calcium (Ca(2+))) cation carriers (i.e., lithium‐metal, lithium‐sulfur, sodium‐metal, potassium‐ion, magnesium‐ion, zinc‐metal, aluminum‐ion, and calcium‐ion batteries) compared to those of liquid counterparts.
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spelling pubmed-106462872023-09-24 Li, Na, K, Mg, Zn, Al, and Ca Anode Interface Chemistries Developed by Solid‐State Electrolytes Shinde, Sambhaji S. Wagh, Nayantara K. Kim, Sung‐Hae Lee, Jung‐Ho Adv Sci (Weinh) Reviews Solid‐state batteries (SSBs) have received significant attention due to their high energy density, reversible cycle life, and safe operations relative to commercial Li‐ion batteries using flammable liquid electrolytes. This review presents the fundamentals, structures, thermodynamics, chemistries, and electrochemical kinetics of desirable solid electrolyte interphase (SEI) required to meet the practical requirements of reversible anodes. Theoretical and experimental insights for metal nucleation, deposition, and stripping for the reversible cycling of metal anodes are provided. Ion transport mechanisms and state‐of‐the‐art solid‐state electrolytes (SEs) are discussed for realizing high‐performance cells. The interface challenges and strategies are also concerned with the integration of SEs, anodes, and cathodes for large‐scale SSBs in terms of physical/chemical contacts, space‐charge layer, interdiffusion, lattice‐mismatch, dendritic growth, chemical reactivity of SEI, current collectors, and thermal instability. The recent innovations for anode interface chemistries developed by SEs are highlighted with monovalent (lithium (Li(+)), sodium (Na(+)), potassium (K(+))) and multivalent (magnesium (Mg(2+)), zinc (Zn(2+)), aluminum (Al(3+)), calcium (Ca(2+))) cation carriers (i.e., lithium‐metal, lithium‐sulfur, sodium‐metal, potassium‐ion, magnesium‐ion, zinc‐metal, aluminum‐ion, and calcium‐ion batteries) compared to those of liquid counterparts. John Wiley and Sons Inc. 2023-09-24 /pmc/articles/PMC10646287/ /pubmed/37743719 http://dx.doi.org/10.1002/advs.202304235 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Shinde, Sambhaji S.
Wagh, Nayantara K.
Kim, Sung‐Hae
Lee, Jung‐Ho
Li, Na, K, Mg, Zn, Al, and Ca Anode Interface Chemistries Developed by Solid‐State Electrolytes
title Li, Na, K, Mg, Zn, Al, and Ca Anode Interface Chemistries Developed by Solid‐State Electrolytes
title_full Li, Na, K, Mg, Zn, Al, and Ca Anode Interface Chemistries Developed by Solid‐State Electrolytes
title_fullStr Li, Na, K, Mg, Zn, Al, and Ca Anode Interface Chemistries Developed by Solid‐State Electrolytes
title_full_unstemmed Li, Na, K, Mg, Zn, Al, and Ca Anode Interface Chemistries Developed by Solid‐State Electrolytes
title_short Li, Na, K, Mg, Zn, Al, and Ca Anode Interface Chemistries Developed by Solid‐State Electrolytes
title_sort li, na, k, mg, zn, al, and ca anode interface chemistries developed by solid‐state electrolytes
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646287/
https://www.ncbi.nlm.nih.gov/pubmed/37743719
http://dx.doi.org/10.1002/advs.202304235
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