Abstract

All-solid-state lithium-ion battery (LiB) is expected as one of the next generation energy storage devices because of their high energy density, high safety and excellent cycle stability. Although oxide-based solid electrolyte materials have rather lower conductivity and poor deformability than sulfide-based one, they have other advantages such as their chemical stability and easiness for handling. Among the various oxide-based SEs, lithium stuffed garnet-type oxide with the formula of Li7La3Zr2O12 (LLZ) have been widely studied because of their high conductivity above 10-4 Scm-1 at room temperature, excellent thermal performance and stability against Li metal anode.Here, we present our recent progress for the development of garnet-type solid electrolytes with high conductivity by simultaneous substitution of Ta5+ into Zr4+ site and Ba2+ into La3+ site in LLZ. Li+ concentration was fixed to 6.5 per chemical formulae, so that the formulae of our Li garnet-type oxide is expressed as Li6.5La3-xBaxZr1.5-xTa0.5+xO12 (LLBZT) and Ba contents x are changed from 0 to 0.3. As results, all LLBZT samples have cubic garnet structure without containing any secondary phases. The lattice parameters of LLBZT decrease with increasing Ba2+ contents x < 0.10 while increase with x from 0.10 to 0.30, possibly due to the simultaneous change of Ba2+ and Ta5+ substitution levels. Relative densities of LLBZT are in the range between 89% and 93% and not influenced so much by the compositions. From AC impedance spectroscopy measurements, the total (bulk + grain) conductivity at 27oC of LLBZT shows its maximum value of 8.34 x 10-4 S cm-1 at x = 0.10, which is slightly higher than the conductivity (= 7.94 x 10-4 S cm-1) of LLZT without substituting Ba (x = 0). Activation energy of the conductivity tends to become lower by Ba substation, while excess Ba substitution degrades the conductivity in LLBZT. LLBZT has wide electrochemical potential window of 0-6 V vs. Li+/Li and reversible Li+ insertion and extraction reactions of TiNb2O7 film electrode formed on LLBZT by aerosol deposition are successfully demonstrated at 60oC. The results indicate that LLBZT can potentially be used as a solid electrolyte in all-solid-state batteries.

Highlights

  • Lithium-ion batteries (LIBs) consist of a graphite negative electrode, organic liquid electrolyte, and lithium transition-metal oxide

  • We investigate the properties of garnet-type Li+ conducting oxide solid electrolyte (SE) with simultaneous substitution of Ta5+ into the Zr4+ site and Ba2+ into the La3+ site in LLZ

  • Li+ concentration was fixed to 6.5 per chemical formulae, so that the composition of our samples is expressed as Li6.5La3−xBaxZr1.5−xTa0.5+xO12 (LLBZT), and Ba contents x are changed from 0 to 0.30

Read more

Summary

Introduction

Lithium-ion batteries (LIBs) consist of a graphite negative electrode, organic liquid electrolyte, and lithium transition-metal oxide. They were first commercialized in 1991, and since such batteries have been widely distributed globally as a power source for mobile electronic devices, such as cell phones and laptop computers. Increasing battery size creates more serious safety issues for LIBs; one reason being the increased amount of flammable organic liquid electrolytes. All-solid-state LIBs are expected to be one of the generations of energy storage devices because of their high energy density, high safety, and excellent cycle stability (Fergus, 2010; Takada, 2013; Tatsumisago et al, 2013).

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.