Enabling High-Stability of Aqueous-Processed Nickel-Rich Positive Electrodes in Lithium Metal Batteries.

Ni-rich cathodes aqueous binders ionic liquid electrolytes lithium batteries lithium metal

Journal

Small (Weinheim an der Bergstrasse, Germany)
ISSN: 1613-6829
Titre abrégé: Small
Pays: Germany
ID NLM: 101235338

Informations de publication

Date de publication:
Oct 2022
Historique:
revised: 16 08 2022
received: 22 06 2022
pubmed: 19 9 2022
medline: 19 9 2022
entrez: 18 9 2022
Statut: ppublish

Résumé

Lithium batteries occupy the large-scale electric mobility market raising concerns about the environmental impact of cell production, especially regarding the use of poly(vinylidene difluoride) (teratogenic) and N-methyl-2-pyrrolidone (NMP, harmful). To avoid their use, an aqueous electrode processing route is utilized in which a water-soluble hybrid acrylic-fluoropolymer together with sodium carboxymethyl cellulose is used as binder, and a thin phosphate coating layer is in situ formed on the surface of the nickel-rich cathode during electrode processing. The resulting electrodes achieve a comparable performance to that of NMP-based electrodes in conventional organic carbonate-based electrolyte (LP30). Subsequently, an ionic liquid electrolyte (ILE) is employed to replace the organic electrolyte, building stable electrode/electrolyte interphases on the surface of the nickel-rich positive electrode (cathode) and metallic lithium negative electrode (anode). In such ILE, the aqueously processed electrodes achieve high cycling stability with a capacity retention of 91% after 1000 cycles (20 °C). In addition, a high capacity of more than 2.5 mAh cm

Identifiants

pubmed: 36116115
doi: 10.1002/smll.202203874
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2203874

Subventions

Organisme : Chinese Scholarship Council
Organisme : Helmholtz Association and the German Federal Ministry of Education and Research
Organisme : within the LILLINT
ID : 03XP0225D
Organisme : National Research Foundation of Korea
Organisme : Korea government
ID : NRF-2020R1A2C2009057
Organisme : Korea government
ID : NRF- 2021R1A4A200168711

Informations de copyright

© 2022 The Authors. Small published by Wiley-VCH GmbH.

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Auteurs

Fanglin Wu (F)

Helmholtz Institute Ulm (HIU) Electrochemical Energy Storage, Helmholtzstrasse 11, 89081, Ulm, Germany.
Karlsruhe Institute of Technology (KIT), P. O. Box 3640, 76021, Karlsruhe, Germany.

Matthias Kuenzel (M)

Helmholtz Institute Ulm (HIU) Electrochemical Energy Storage, Helmholtzstrasse 11, 89081, Ulm, Germany.
Karlsruhe Institute of Technology (KIT), P. O. Box 3640, 76021, Karlsruhe, Germany.

Thomas Diemant (T)

Helmholtz Institute Ulm (HIU) Electrochemical Energy Storage, Helmholtzstrasse 11, 89081, Ulm, Germany.
Karlsruhe Institute of Technology (KIT), P. O. Box 3640, 76021, Karlsruhe, Germany.

Angelo Mullaliu (A)

Helmholtz Institute Ulm (HIU) Electrochemical Energy Storage, Helmholtzstrasse 11, 89081, Ulm, Germany.
Karlsruhe Institute of Technology (KIT), P. O. Box 3640, 76021, Karlsruhe, Germany.

Shan Fang (S)

Helmholtz Institute Ulm (HIU) Electrochemical Energy Storage, Helmholtzstrasse 11, 89081, Ulm, Germany.
Karlsruhe Institute of Technology (KIT), P. O. Box 3640, 76021, Karlsruhe, Germany.

Jae-Kwang Kim (JK)

Department of Solar & Energy Engineering, Cheongju University, Cheongju, Chungbuk, 28503, Republic of Korea.

Hee Woong Kim (HW)

Department of Solar & Energy Engineering, Cheongju University, Cheongju, Chungbuk, 28503, Republic of Korea.

Guk-Tae Kim (GT)

Helmholtz Institute Ulm (HIU) Electrochemical Energy Storage, Helmholtzstrasse 11, 89081, Ulm, Germany.
Karlsruhe Institute of Technology (KIT), P. O. Box 3640, 76021, Karlsruhe, Germany.

Stefano Passerini (S)

Helmholtz Institute Ulm (HIU) Electrochemical Energy Storage, Helmholtzstrasse 11, 89081, Ulm, Germany.
Karlsruhe Institute of Technology (KIT), P. O. Box 3640, 76021, Karlsruhe, Germany.

Classifications MeSH