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Enabling Aqueous Processing of Ni‐Rich Layered Oxide Cathode Materials by Addition of Lithium Sulfate

Aqueous processing of Ni‐rich layered oxide cathode materials is a promising approach to simultaneously decrease electrode manufacturing costs, while bringing environmental benefits by substituting the state‐of‐the‐art (often toxic and costly) organic processing solvents. However, an aqueous environ...

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Autores principales: Heidbüchel, Marcel, Schultz, Thorsten, Placke, Tobias, Winter, Martin, Koch, Norbert, Schmuch, Richard, Gomez‐Martin, Aurora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107986/
https://www.ncbi.nlm.nih.gov/pubmed/36445782
http://dx.doi.org/10.1002/cssc.202202161
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author Heidbüchel, Marcel
Schultz, Thorsten
Placke, Tobias
Winter, Martin
Koch, Norbert
Schmuch, Richard
Gomez‐Martin, Aurora
author_facet Heidbüchel, Marcel
Schultz, Thorsten
Placke, Tobias
Winter, Martin
Koch, Norbert
Schmuch, Richard
Gomez‐Martin, Aurora
author_sort Heidbüchel, Marcel
collection PubMed
description Aqueous processing of Ni‐rich layered oxide cathode materials is a promising approach to simultaneously decrease electrode manufacturing costs, while bringing environmental benefits by substituting the state‐of‐the‐art (often toxic and costly) organic processing solvents. However, an aqueous environment remains challenging due to the high reactivity of Ni‐rich layered oxides towards moisture, leading to lithium leaching and Al current collector corrosion because of the resulting high pH value of the aqueous electrode paste. Herein, a facile method was developed to enable aqueous processing of LiNi(0.8)Co(0.1)Mn(0.1)O(2) (NCM811) by the addition of lithium sulfate (Li(2)SO(4)) during electrode paste dispersion. The aqueously processed electrodes retained 80 % of their initial capacity after 400 cycles in NCM811||graphite full cells, while electrodes processed without the addition of Li(2)SO(4) reached 80 % of their capacity after only 200 cycles. Furthermore, with regard to electrochemical performance, aqueously processed electrodes using carbon‐coated Al current collector outperformed reference electrodes based on state‐of‐the‐art production processes involving N‐methyl‐2‐pyrrolidone as processing solvent and fluorinated binders. The positive impact on cycle life by the addition of Li(2)SO(4) stemmed from a formed sulfate coating as well as different surface species, protecting the NCM811 surface against degradation. Results reported herein open a new avenue for the processing of Ni‐rich NCM electrodes using more sustainable aqueous routes.
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spelling pubmed-101079862023-04-18 Enabling Aqueous Processing of Ni‐Rich Layered Oxide Cathode Materials by Addition of Lithium Sulfate Heidbüchel, Marcel Schultz, Thorsten Placke, Tobias Winter, Martin Koch, Norbert Schmuch, Richard Gomez‐Martin, Aurora ChemSusChem Research Articles Aqueous processing of Ni‐rich layered oxide cathode materials is a promising approach to simultaneously decrease electrode manufacturing costs, while bringing environmental benefits by substituting the state‐of‐the‐art (often toxic and costly) organic processing solvents. However, an aqueous environment remains challenging due to the high reactivity of Ni‐rich layered oxides towards moisture, leading to lithium leaching and Al current collector corrosion because of the resulting high pH value of the aqueous electrode paste. Herein, a facile method was developed to enable aqueous processing of LiNi(0.8)Co(0.1)Mn(0.1)O(2) (NCM811) by the addition of lithium sulfate (Li(2)SO(4)) during electrode paste dispersion. The aqueously processed electrodes retained 80 % of their initial capacity after 400 cycles in NCM811||graphite full cells, while electrodes processed without the addition of Li(2)SO(4) reached 80 % of their capacity after only 200 cycles. Furthermore, with regard to electrochemical performance, aqueously processed electrodes using carbon‐coated Al current collector outperformed reference electrodes based on state‐of‐the‐art production processes involving N‐methyl‐2‐pyrrolidone as processing solvent and fluorinated binders. The positive impact on cycle life by the addition of Li(2)SO(4) stemmed from a formed sulfate coating as well as different surface species, protecting the NCM811 surface against degradation. Results reported herein open a new avenue for the processing of Ni‐rich NCM electrodes using more sustainable aqueous routes. John Wiley and Sons Inc. 2022-12-14 2023-01-20 /pmc/articles/PMC10107986/ /pubmed/36445782 http://dx.doi.org/10.1002/cssc.202202161 Text en © 2022 The Authors. ChemSusChem 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 Research Articles
Heidbüchel, Marcel
Schultz, Thorsten
Placke, Tobias
Winter, Martin
Koch, Norbert
Schmuch, Richard
Gomez‐Martin, Aurora
Enabling Aqueous Processing of Ni‐Rich Layered Oxide Cathode Materials by Addition of Lithium Sulfate
title Enabling Aqueous Processing of Ni‐Rich Layered Oxide Cathode Materials by Addition of Lithium Sulfate
title_full Enabling Aqueous Processing of Ni‐Rich Layered Oxide Cathode Materials by Addition of Lithium Sulfate
title_fullStr Enabling Aqueous Processing of Ni‐Rich Layered Oxide Cathode Materials by Addition of Lithium Sulfate
title_full_unstemmed Enabling Aqueous Processing of Ni‐Rich Layered Oxide Cathode Materials by Addition of Lithium Sulfate
title_short Enabling Aqueous Processing of Ni‐Rich Layered Oxide Cathode Materials by Addition of Lithium Sulfate
title_sort enabling aqueous processing of ni‐rich layered oxide cathode materials by addition of lithium sulfate
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107986/
https://www.ncbi.nlm.nih.gov/pubmed/36445782
http://dx.doi.org/10.1002/cssc.202202161
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