Affiliation:
1. School of Advanced Materials Peking University Shenzhen Graduate School Shenzhen 518055 China
2. Advanced Technology Institute University of Surrey Guildford Surrey GU2 7XH UK
3. Department of Mechanical and Materials Engineering University of Western Ontario London ON N6A 5B9 Canada
Abstract
AbstractHigh Li+ conductivity, good interfacial compatibility and high mechanical strength are desirable for practical utilization of all‐solid‐state electrolytes. In this study, by introducing Li6.4La3Zr1.4Ta0.6O12 (LLZTO) with surface defects into poly(ethylene oxide) (PEO), a composite solid electrolyte (OV‐LLZTO/PEO) is prepared. The surface defects serve as anchoring points for oxygen atoms of PEO chains, forming a firmly bonded polymer‐ceramic interface. This bonding effect effectively prevents the agglomeration of LLZTO particles and crystallization of PEO domains, forming a homogeneous electrolyte membrane exhibiting high mechanical strength, reduced interfacial resistance with electrodes as well as improved Li+ conductivity. Owing to these favorable properties, OV‐LLZTO/PEO can be operated under a high current density (0.7 mA cm−2) in a Li–Li symmetric cell without short circuit. Above all, solid‐state full‐cells employing OV‐LLZTO/PEO deliver state‐of‐the‐art rate capability (8 C), power density and capacity retention. As a final proof of concept study, flexible pouch cells are assembled and tested, exhibiting high cycle stability under 5 C and excellent safety feature under abusive working conditions. Through manipulating the interfacial interactions between polymer and inorganic electrolytes, this study points out a new direction to optimizing the performance of all‐solid‐state batteries.
Subject
Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials
Cited by
45 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献