Abstract

High-energy-density batteries are actively sought after for next-generation electric vehicle applications, triggering the search for sulfur-based positive electrode materials with high capacity for extended driving range. One of the primary issues of sulfur cathodes is the rapid capacity decay caused by the dissolution of sulfur in the electrolyte and the resulting parasitic reactions. This can be prevented by incorporating a suitable amount of carbon material into the sulfur electrodes, because of its inherent properties; however, introducing a large amount of low-density carbon materials will lead to a decrease in the energy density of the battery. Therefore, an alternative method to suppress sulfur dissolution is required for commercial applications. Recently, we developed a Fe-containing Li2S-based material (Li8FeS5) as the sulfur cathode; it has a relatively high initial discharge capacity (> 700 mAh∙g-1) and electric conductivity. However, rapid capacity degradation was observed during the initial several cycles, due to some unknown reactions between the electrolyte and Li8FeS5. In this study we demonstrate an effective method to improve the cycle performance of Li8FeS5 by coating its surface with a stabilizing material. We selected titanium oxide as the coating material, based on its high stability toward liquid electrolytes and its strong interaction with sulfur. Hence, we obtained TiOx-coated Li8FeS5 particles (Li8FeS5-TiOx) by a liquid-phase reaction. The Transmission electron microscopy observation revealed that the Li8FeS5 particles were coated with several tens of nanometers of TiOx layers. The Li8FeS5-TiOx cells exhibited improved cycling performance with a carbonate electrolyte. We also observed that the capacity originating from an iron redox was not affected by coating during the cycling test; in contrast, the degradation of the cell capacity corresponding to the sulfur redox was suppressed significantly after coating with the TiOx layer. Thus, the surface reaction of Li8FeS5 with the electrolyte, which could be the main reason for the cycling degradation, was effectively suppressed by coating with the TiOx layer.

Highlights

  • High-energy-density batteries are required for next-generation electric vehicle (EV) applications

  • Even though Li8FeS5 intrinsically showed rather reversible structural changes for Li extraction/insertion reactions, a rapid capacity degradation was observed during the initial several cycles of the Li8FeS5 cathode

  • We focused on improving the cycle performance of Li8FeS5 by coating its surface with titanium oxide (TiOx)

Read more

Summary

INTRODUCTION

High-energy-density batteries are required for next-generation electric vehicle (EV) applications. One of the main limitations to utilizing a sulfur cathode is its electronically insulating nature, which requires compounding with a sufficient amount of electrically-conductive materials in the positive electrode (Obrovac and Dahn, 2002) Another issue is the poor electrochemical performance caused by polysulfide dissolution, which leads to the irreversible loss of active materials from the cathode, low coulombic efficiency, and rapid capacity fading. Even though Li8FeS5 intrinsically showed rather reversible structural changes for Li extraction/insertion reactions, a rapid capacity degradation was observed during the initial several cycles of the Li8FeS5 cathode Considering these XAFS results, it is likely that the relatively unstable surface of Li8FeS5 particles might react with the electrolyte, thereby leading to the initial decay. We compared the electrochemical performances of the pristine Li8FeS5 and TiOx-coated Li8FeS5 (Li8FeS5-TiOx) cells

MATERIALS AND METHODS
AND DISCUSSION
Findings
CONCLUSION

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.