A Perovskite Electrolyte That Is Stable in Moist Air for Lithium‐Ion Batteries

Solid‐oxide Li+ electrolytes of a rechargeable cell are generally sensitive to moisture in the air as H+ exchanges for the mobile Li+ of the electrolyte and forms insulating surface phases at the electrolyte interfaces and in the grain boundaries of a polycrystalline membrane. These surface phases d...

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Published inAngewandte Chemie (International ed.) Vol. 57; no. 28; pp. 8587 - 8591
Main Authors Li, Yutao, Xu, Henghui, Chien, Po‐Hsiu, Wu, Nan, Xin, Sen, Xue, Leigang, Park, Kyusung, Hu, Yan‐Yan, Goodenough, John B.
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 09.07.2018
Wiley Blackwell (John Wiley & Sons)
EditionInternational ed. in English
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Summary:Solid‐oxide Li+ electrolytes of a rechargeable cell are generally sensitive to moisture in the air as H+ exchanges for the mobile Li+ of the electrolyte and forms insulating surface phases at the electrolyte interfaces and in the grain boundaries of a polycrystalline membrane. These surface phases dominate the total interfacial resistance of a conventional rechargeable cell with a solid–electrolyte separator. We report a new perovskite Li+ solid electrolyte, Li0.38Sr0.44Ta0.7Hf0.3O2.95F0.05, with a lithium‐ion conductivity of σLi=4.8×10−4 S cm−1 at 25 °C that does not react with water having 3≤pH≤14. The solid electrolyte with a thin Li+‐conducting polymer on its surface to prevent reduction of Ta5+ is wet by metallic lithium and provides low‐impedance dendrite‐free plating/stripping of a lithium anode. It is also stable upon contact with a composite polymer cathode. With this solid electrolyte, we demonstrate excellent cycling performance of an all‐solid‐state Li/LiFePO4 cell, a Li‐S cell with a polymer‐gel cathode, and a supercapacitor. A perovskite that is stable in water with 3≤pH≤14 shows small interfacial resistance and excellent cycling performance in an all‐solid‐state Li/LiFePO4 cell, a Li‐S cell, and a supercapacitor.
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EE0007762; 7223523
USDOE
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201804114