Fast Lithium Intercalation Mechanism on Surface‐Modified Cathodes for Lithium‐Ion Batteries

Author:

Zhou Huangkai1ORCID,Izumi Jun1,Asano Sho1,Ito Kotaro1,Watanabe Kenta1ORCID,Suzuki Kota2ORCID,Nemoto Fumiya34ORCID,Yamada Norifumi L.3ORCID,Aso Kohei5ORCID,Oshima Yoshifumi5ORCID,Kanno Ryoji2ORCID,Hirayama Masaaki12ORCID

Affiliation:

1. Department of Chemical Science and Engineering School of Materials and Chemical Technology Tokyo Institute of Technology 4259 Nagatsuta‐cho, Midori‐ku Yokohama 226‐8501 Japan

2. All‐Solid‐State Battery Center Institute of Innovative Research Tokyo Institute of Technology 4259 Nagatsuta‐cho, Midori‐ku Yokohama 226‐8501 Japan

3. Institute of Materials Structure Science High Energy Accelerator Research Organization 203‐1 Shirakata Tokai Ibaraki 319‐1106 Japan

4. Department of Materials Science and Engineering National Defense Academy 1‐10‐20 Hashirimizu Yokosuka Kanagawa 239‐8686 Japan

5. Nanomaterials and Devices Research Area School of Materials Science Japan Advanced Institute of Science and Technology Asahidai 1–1, Nomi Ishikawa 923‐1292 Japan

Abstract

AbstractEnhancing the understanding of fast lithium intercalation on cathode surfaces modified by oxides is crucial for the development of electrode materials that offer high‐power and long‐life operation. Herein, lithium transfer is elucidated by directly observing the structural changes within the cathode, through the interface, and into the electrolyte using in situ neutron reflectometry (NR). Two films are studied—a Li2ZrO3‐modified and an unmodified LiCoO2 film—and it is found that the modified film exhibits a superior rate capability. In situ NR studies indicate that the surface modification facilitates the formation of a dense cathode–electrolyte interphase (CEI), primarily composed of inorganic species. In contrast, the unmodified surface is covered by a relatively sparse and electrolyte‐impregnated CEI. These structural observations suggest that lithium desolvation during intercalation primarily occurs on the CEI and LiCoO2 surfaces for the modified and unmodified films, respectively. Fast desolvation of lithium on the CEI may contribute to the superior rate capability of the surface‐modified cathodes. This suggests a mechanism of fast intercalation achieved by surface modification of low ionically conductive oxides. Simultaneous chemical composition and morphological information is a powerful way to elucidate the dynamics at cathode/liquid electrolyte interfaces suitable for high‐power operation.

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

General Materials Science,Renewable Energy, Sustainability and the Environment

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