A Bifunctional Perovskite Promoter for Polysulfide Regulation toward Stable Lithium-Sulfur Batteries.

Kong, Long; Chen, Xiang; Li, Bo-Quan; Peng, Hong-Jie; Huang, Jia-Qi; Xie, Jin; Zhang, Qiang · Adv Mater · 2018

basic_science · Level V

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Abstract

Lithium-sulfur (LiS) batteries are strongly considered as the next-generation rechargeable cells. However, both the shuttle of lithium polysulfides (LiPSs) and sluggish kinetics in random deposition of lithium sulfides (Li<sub>2</sub> S) significantly degrade the capacity, rate performance, and cycling life of LiS cells. Herein, bifunctional Ba<sub>0.5</sub> Sr<sub>0.5</sub> Co<sub>0.8</sub> Fe<sub>0.2</sub> O<sub>3-</sub><sub>δ</sub> perovskite nanoparticles (PrNPs) are proposed as a promoter to immobilize LiPSs and guide the deposition of Li<sub>2</sub> S in a LiS cell. The oxygen vacancy in PrNPs increases the metal reactivity to anchor LiPSs, and co-existence of lithiophilic (O) and sulfiphilic (Sr) sites in PrNP favor the dual-bonding (LiO and SrS bonds) to anchor LiPSs. The high catalytic nature of PrNP facilitates the kinetics of LiPS redox reaction. The PrNP with intrinsic LiPS affinity serves as nucleation sites for Li<sub>2</sub> S deposition and guides its uniform propagation. Therefore, the bifunctional LiPS promoter in LiS cell yields high rate performance and ultralow capacity decay rate of 0.062% (a quarter of pristine LiS cells). The proposed strategy to immobilize LiPSs, promotes the conversion of LiPS, and regulates deposition of Li<sub>2</sub> S by an emerging perovskite promoter and is also expected to be applied in other energy conversion and storage devices based on multi-electron redox reactions.