Combating Li metal deposits in all-solid-state battery via the piezoelectric and ferroelectric effects

Author:

Tao Jianming1234ORCID,Chen Yue5ORCID,Bhardwaj Aman3,Wen Lang124,Li Jiaxin1246,Kolosov Oleg V.5ORCID,Lin Yingbin1246,Hong Zhensheng1237ORCID,Huang Zhigao1246,Mathur Sanjay3

Affiliation:

1. College of Physics and Energy, Fujian Normal University, Fuzhou 350117, China

2. Fujian Provincial Solar Energy Conversion and Energy Storage Engineering Technology Research Center, Fuzhou 350117, China

3. Institute of Inorganic Chemistry, University of Cologne, Greinstr.6, 50939 Cologne, Germany

4. Fujian Provincial Key Laboratory of Quantum Manipulation and New Energy Materials, Fuzhou 350117, China

5. Physics Department, Lancaster University, Lancaster LA1 4YB, United Kingdom

6. Fujian Provincial Collaborative Innovation Center for Advanced High-Field Superconducting Materials and Engineering, Fuzhou 350117, China

7. Academy of Carbon Neutrality, Fujian Normal University, Fuzhou 350117, China

Abstract

All-solid-state Li-metal batteries (ASSLBs) are highly desirable, due to their inherent safety and high energy density; however, the irregular and uncontrolled growth of Li filaments is detrimental to interfacial stability and safety. Herein, we report on the incorporation of piezo-/ferroelectric BaTiO 3 (BTO) nanofibers into solid electrolytes and determination of electric-field distribution due to BTO inclusion that effectively regulates the nucleation and growth of Li dendrites. Theoretical simulations predict that the piezoelectric effect of BTO embedded in solid electrolyte reduces the driving force of dendrite growth at high curvatures, while its ferroelectricity reduces the overpotential, which helps to regularize Li deposition and Li + flux. Polarization reversal of soft solid electrolytes was identified, confirming a regular deposition and morphology alteration of Li. As expected, the ASSLBs operating with LiFePO 4 /Li and poly(ethylene oxide) (PEO)/garnet solid electrolyte containing 10% BTO additive showed a steady and long cycle life with a reversible capacity of 103.2 mAh g −1 over 500 cycles at 1 C. Furthermore, the comparable cyclability and flexibility of the scalable pouch cells prepared and the successful validation in the sulfide electrolytes, demonstrating its universal and promising application for the integration of Li metal anodes in solid-state batteries.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Fujian Province

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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