In Situ Li<sub>3</sub>PS<sub>4</sub> Solid‐State Electrolyte Protection Layers for Superior Long‐Life and High‐Rate Lithium‐Metal Anodes

Jianwen Liang, Xiaona Li, Yang Zhao, Lyudmila V. Goncharova, Gongming Wang, Keegan R. Adair, Changhong Wang, Ruying Li, Yongchun Zhu, Yitai Qian,

Advanced Materials · 2018 · 180 citations · 51 references

Concepts

Abstract

Abstract A thin and adjustable Li 3 PS 4 (LPS) solid‐state electrolyte protection layer on the surface of Li is proposed to address the dynamic plating/stripping process of Li metal. The LPS interlayer is formed by an in situ and self‐limiting reaction between P 4 S 16 and Li in N ‐methyl‐2‐pyrrolidone. By increasing the concentration of P 4 S 16 , the thickness of the LPS layer can be adjusted up to 60 nm. Due to the high ionic conductivity and low electrochemical activity of Li 3 PS 4 , the intimate protection layer of LPS can not only prevent the formation of Li dendrites, but also reduces parasitic side reactions and improves the electrochemical performance. As a result, symmetric cells with the LPS protection layer can deliver stable Li plating/stripping for 2000 h. Full cells assembled with the LPS‐protected Li exhibit two times higher capacity retention in Li–S batteries (≈800 mAh g −1 ) at 5 A g −1 for over 400 cycles compared to their bare Li counterparts. Furthermore, high rate performances can be achieved with Li‐LPS/LiCoO 2 cells, which are capable of cycling at rates as high as 20 C. This innovative and scalable approach to stabilizing the Li anode can serve as a basis for the development of next‐generation high‐performance lithium‐metal batteries.

References

51