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Fabrication of Oxide-Based All-Solid-State Batteries by a Sintering Process Based on Function Sharing of Solid Electrolytes

[Image: see text] Garnet-type Li(7)La(3)Zr(2)O(12) (LLZ) has advantages of stability with Li metal and high Li(+) ionic conductivity, achieving 1 × 10(–3) S cm(–1), but it is prone to react with electrode active materials during the sintering process. LISICON-type Li(3.5)Ge(0.5)V(0.5)O(4) (LGVO) has...

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Autores principales: Sakakura, Miyuki, Mitsuishi, Kazutaka, Okumura, Toyoki, Ishigaki, Norikazu, Iriyama, Yasutoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635363/
https://www.ncbi.nlm.nih.gov/pubmed/36191087
http://dx.doi.org/10.1021/acsami.2c10853
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author Sakakura, Miyuki
Mitsuishi, Kazutaka
Okumura, Toyoki
Ishigaki, Norikazu
Iriyama, Yasutoshi
author_facet Sakakura, Miyuki
Mitsuishi, Kazutaka
Okumura, Toyoki
Ishigaki, Norikazu
Iriyama, Yasutoshi
author_sort Sakakura, Miyuki
collection PubMed
description [Image: see text] Garnet-type Li(7)La(3)Zr(2)O(12) (LLZ) has advantages of stability with Li metal and high Li(+) ionic conductivity, achieving 1 × 10(–3) S cm(–1), but it is prone to react with electrode active materials during the sintering process. LISICON-type Li(3.5)Ge(0.5)V(0.5)O(4) (LGVO) has the advantage of less reactivity with the electrode active material during the sintering process, but its ionic conductivity is on the order of 10(–5) S cm(–1). In this study, these two solid electrolytes are combined as a multilayer solid electrolyte sheet, where 2 μm thick LGVO films are coated on LLZ sheets to utilize the advantages of these two solid electrolytes. These two solid electrolytes adhere well through Ge diffusion without significant interfacial resistance. The LLZ–LGVO multilayer is combined with a LiCoO(2) positive electrode and a lithium metal anode through annealing at 700 °C. The resultant all-solid-state battery can undergo repeated charge–discharge reactions for over 100 cycles at 25 or 60 °C. The LGVO coating suppresses the increases in the resistance from the solid electrolyte and interfacial resistance induced by annealing by ca. 1/40. As with sulfide-based all-solid-state batteries, function sharing of solid electrolytes will be a promising method for developing advanced oxide-based all-solid-state batteries through a sintering process.
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spelling pubmed-96353632023-10-03 Fabrication of Oxide-Based All-Solid-State Batteries by a Sintering Process Based on Function Sharing of Solid Electrolytes Sakakura, Miyuki Mitsuishi, Kazutaka Okumura, Toyoki Ishigaki, Norikazu Iriyama, Yasutoshi ACS Appl Mater Interfaces [Image: see text] Garnet-type Li(7)La(3)Zr(2)O(12) (LLZ) has advantages of stability with Li metal and high Li(+) ionic conductivity, achieving 1 × 10(–3) S cm(–1), but it is prone to react with electrode active materials during the sintering process. LISICON-type Li(3.5)Ge(0.5)V(0.5)O(4) (LGVO) has the advantage of less reactivity with the electrode active material during the sintering process, but its ionic conductivity is on the order of 10(–5) S cm(–1). In this study, these two solid electrolytes are combined as a multilayer solid electrolyte sheet, where 2 μm thick LGVO films are coated on LLZ sheets to utilize the advantages of these two solid electrolytes. These two solid electrolytes adhere well through Ge diffusion without significant interfacial resistance. The LLZ–LGVO multilayer is combined with a LiCoO(2) positive electrode and a lithium metal anode through annealing at 700 °C. The resultant all-solid-state battery can undergo repeated charge–discharge reactions for over 100 cycles at 25 or 60 °C. The LGVO coating suppresses the increases in the resistance from the solid electrolyte and interfacial resistance induced by annealing by ca. 1/40. As with sulfide-based all-solid-state batteries, function sharing of solid electrolytes will be a promising method for developing advanced oxide-based all-solid-state batteries through a sintering process. American Chemical Society 2022-10-03 2022-11-02 /pmc/articles/PMC9635363/ /pubmed/36191087 http://dx.doi.org/10.1021/acsami.2c10853 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Sakakura, Miyuki
Mitsuishi, Kazutaka
Okumura, Toyoki
Ishigaki, Norikazu
Iriyama, Yasutoshi
Fabrication of Oxide-Based All-Solid-State Batteries by a Sintering Process Based on Function Sharing of Solid Electrolytes
title Fabrication of Oxide-Based All-Solid-State Batteries by a Sintering Process Based on Function Sharing of Solid Electrolytes
title_full Fabrication of Oxide-Based All-Solid-State Batteries by a Sintering Process Based on Function Sharing of Solid Electrolytes
title_fullStr Fabrication of Oxide-Based All-Solid-State Batteries by a Sintering Process Based on Function Sharing of Solid Electrolytes
title_full_unstemmed Fabrication of Oxide-Based All-Solid-State Batteries by a Sintering Process Based on Function Sharing of Solid Electrolytes
title_short Fabrication of Oxide-Based All-Solid-State Batteries by a Sintering Process Based on Function Sharing of Solid Electrolytes
title_sort fabrication of oxide-based all-solid-state batteries by a sintering process based on function sharing of solid electrolytes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635363/
https://www.ncbi.nlm.nih.gov/pubmed/36191087
http://dx.doi.org/10.1021/acsami.2c10853
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