High-performance all-solid-state batteries enabled by salt bonding to perovskite in poly(ethylene oxide).

Xu, Henghui; Chien, Po-Hsiu; Shi, Jianjian; Li, Yutao; Wu, Nan; Liu, Yuanyue; Hu, Yan-Yan; Goodenough, John B · Proc Natl Acad Sci U S A · 2019

basic_science · Level V

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Abstract

Flexible and low-cost poly(ethylene oxide) (PEO)-based electrolytes are promising for all-solid-state Li-metal batteries because of their compatibility with a metallic lithium anode. However, the low room-temperature Li-ion conductivity of PEO solid electrolytes and severe lithium-dendrite growth limit their application in high-energy Li-metal batteries. Here we prepared a PEO/perovskite Li<sub>3/8</sub>Sr<sub>7/16</sub>Ta<sub>3/4</sub>Zr<sub>1/4</sub>O<sub>3</sub> composite electrolyte with a Li-ion conductivity of 5.4 × 10<sup>-5</sup> and 3.5 × 10<sup>-4</sup> S cm<sup>-1</sup> at 25 and 45 °C, respectively; the strong interaction between the F<sup>-</sup> of TFSI<sup>-</sup> (bis-trifluoromethanesulfonimide) and the surface Ta<sup>5+</sup> of the perovskite improves the Li-ion transport at the PEO/perovskite interface. A symmetric Li/composite electrolyte/Li cell shows an excellent cyclability at a high current density up to 0.6 mA cm<sup>-2</sup> A solid electrolyte interphase layer formed in situ between the metallic lithium anode and the composite electrolyte suppresses lithium-dendrite formation and growth. All-solid-state Li|LiFePO<sub>4</sub> and high-voltage Li|LiNi<sub>0.8</sub>Mn<sub>0.1</sub>Co<sub>0.1</sub>O<sub>2</sub> batteries with the composite electrolyte have an impressive performance with high Coulombic efficiencies, small overpotentials, and good cycling stability.