Origin of O2 Generation in Sulfide‐Based All‐Solid‐State Batteries and its Impact on High Energy Density

Author:

Yoshikawa Keisuke1,Kato Takeshi1,Suzuki Yasuhiro1,Shiota Akihiro2,Ohnishi Tsuyoshi3,Amezawa Koji4,Nakao Aiko1,Yajima Takeshi1,Iriyama Yasutoshi1ORCID

Affiliation:

1. Department of Material Design Innovation Engineering Graduate School of Engineering Nagoya University Furo‐cho, Chikusa‐ku Nagoya Aichi 464‐8603 Japan

2. Consortium for Lithium Ion Battery Technology and Evaluation Center (LIBTEC) 1‐8‐31 Midorigaoka Ikeda Osaka 563‐8577 Japan

3. Center for Green Research on Energy and Environmental Materials National Institute for Materials Science (NIMS) 1‐1 Namiki Tsukuba Ibaraki 305‐0044 Japan

4. Institute of Multidisciplinary Research for Advanced Materials Tohoku University 2‐1‐1, Katahira, Aoba‐Ku Sendai Miyagi 980‐8577 Japan

Abstract

AbstractThe cathode surface of sulfide‐based all‐solid‐state batteries (SBs) is commonly coated with amorphous‐LiNbO3 in order to stabilize charge–discharge reactions. However, high‐voltage charging diminishes the advantages, which is caused by problems with the amorphous‐LiNbO3 coating layer. This study has investigated the degradation of amorphous‐LiNbO3 coating layer directly during the high‐voltage charging of SBs. O2 generation via Li extraction from the amorphous‐LiNbO3 coating layer is observed using electrochemical gas analysis and electrochemical X‐ray photoelectron spectroscopy. This O2 leads to the formation of an oxidative solid electrolyte (SE) around the coating layer and degrades the battery performance. On the other hand, elemental substitution (i.e., amorphous‐LiNbxP1‐xO3) reduces O2 release, leading to stable high‐voltage charge–discharge reactions of SBs. The results have emphasized that the suppression of O2 generation is a key factor in improving the energy density of SBs.

Funder

Japan Society for the Promotion of Science London

New Energy and Industrial Technology Development Organization

Publisher

Wiley

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