Taming Metal–Solid Electrolyte Interface Instability via Metal Strain Hardening

Author:

Zhao Lihong1,Li Wei2,Wu Chaoshan3,Ai Qing4,Guo Liqun13,Chen Zhaoyang13,Zheng Jie13,Anderson Matthew1,Guo Hua4,Lou Jun4,Liang Yanliang1,Fan Zheng5,Zhu Juner2,Yao Yan1ORCID

Affiliation:

1. Department of Electrical and Computer Engineering and Texas Center for Superconductivity at the University of Houston University of Houston Houston 77204 TX USA

2. Department of Mechanical and Industrial Engineering Northeastern University Boston 02115 MA USA

3. Materials Science and Engineering Program University of Houston Houston 77204 TX USA

4. Department of Materials Science and Nanoengineering Rice University Houston 77005 TX USA

5. Department of Engineering Technology University of Houston Houston 77204 TX USA

Abstract

AbstractSolid‐state lithium metal batteries have emerged as a promising technology for electric vehicles due to their high specific energy and safety potential. Obtaining intimate contact between Li and electrolyte during cell fabrication, however, remains challenging. Adequate fabrication pressure is required to promote close contact, but this pressure can cause Li deformation and penetration into the electrolyte, resulting in poor battery performance. Here, a strategy for addressing this problem is presented by incorporating 3 at% Mg into Li. Unlike pure Li which obeys the Voce hardening law and allows unconstrained deformation, Li─Mg alloy follows the Swift hardening law and strengthens with strain under compression stress. Because of the constrained deformation of Li─Mg, intimate contact with solid electrolytes is possible even at high fabrication pressure (50–65 MPa), resulting in high critical current densities. These findings underscore the importance of understanding Li metal deformation properties to improve solid‐state battery performance.

Publisher

Wiley

Subject

General Materials Science,Renewable Energy, Sustainability and the Environment

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