Oxygen Substitution to Enhance Chemo-Mechanical Stability at the Cathode-Sulfide Electrolyte Interface in All-Solid-State Batteries

The high interface resistance at the cathode-sulfide electrolyte interface is still a crucial drawback in an all-solid-state battery, unlike the initial expectation that the all-solid-state interface would enhance electrochemical stability by reducing side reactions at the interface. In this study, we examined the fundamental mechanism of unexpected reactions at the interface of LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub> (NCM811) and argyrodite (Li<sub>6</sub>PS<sub>5</sub>Br<sub>0.5</sub>Cl<sub>0.5</sub>, LPSBC) sulfide solid electrolytes based on the combined method of multiscale simulations and electrochemical experiments. The high interface resistance originates from the formation of a passivating layer at the interface combined with irregular atomic and electronic structures, Li depletion, mutual element exchange, and mechanical contact loss between the oxide cathode and sulfide solid electrolyte. We also confirmed that these side reactions were suppressed by O substitutions to sulfide solid electrolyte (LPSOBC), and then the chemo-mechanical stability of the all-solid battery was enhanced by alleviating the side reactions at the interface. This study provides rational insights into the design of an interface for all-solid-state batteries.

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Publication Details

Journal
ACS Nano
Published
2024-08-16
DOI
https://doi.org/10.1021/acsnano.4c06345
Citations
14
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
2.92

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article

Oxygen Substitution to Enhance Chemo-Mechanical Stability at the Cathode-Sulfide Electrolyte Interface in All-Solid-State Batteries

Kyeongjae Cho, You‐Jin Lee, So-Ri Lee, Heetaek Park et al.
14 citations
ACS Nano
Advancements in Battery Materials
2.92
article

Oxygen Substitution to Enhance Chemo-Mechanical Stability at the Cathode-Sulfide Electrolyte Interface in All-Solid-State Batteries

Kyeongjae Cho, You‐Jin Lee, So-Ri Lee, Heetaek Park, Jong-Hyuk Bae, Taesoon Hwang, Yoon‐Cheol Ha, Jun-Woo Park
article en
14 citations

Abstract

The high interface resistance at the cathode-sulfide electrolyte interface is still a crucial drawback in an all-solid-state battery, unlike the initial expectation that the all-solid-state interface would enhance electrochemical stability by reducing side reactions at the interface. In this study, we examined the fundamental mechanism of unexpected reactions at the interface of LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub> (NCM811) and argyrodite (Li<sub>6</sub>PS<sub>5</sub>Br<sub>0.5</sub>Cl<sub>0.5</sub>, LPSBC) sulfide solid electrolytes based on the combined method of multiscale simulations and electrochemical experiments. The high interface resistance originates from the formation of a passivating layer at the interface combined with irregular atomic and electronic structures, Li depletion, mutual element exchange, and mechanical contact loss between the oxide cathode and sulfide solid electrolyte. We also confirmed that these side reactions were suppressed by O substitutions to sulfide solid electrolyte (LPSOBC), and then the chemo-mechanical stability of the all-solid battery was enhanced by alleviating the side reactions at the interface. This study provides rational insights into the design of an interface for all-solid-state batteries.

ACS NanoVol. 18(34)
The University of Texas at Dallas (US), Korea Electrotechnology Research Institute (KR)
Ministry of Trade, Industry and Energy, Korea Electrotechnology Research Institute, University of Texas at Dallas
Affordable and clean energy
Openalex Percentile: Top 9%
Advancements in Battery Materials
2.92
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