金属锂
电解质
锂(药物)
兴奋剂
材料科学
固态
金属
化学工程
纳米技术
光电子学
工程物理
物理化学
化学
电极
冶金
物理
工程类
医学
内分泌学
作者
Sihan Chen,Jun Li,Keke Liu,Xiaochen Sun,Jingwei Wan,Huiyu Zhai,Xinfeng Tang,Gangjian Tan
标识
DOI:10.1088/1674-1056/ad41b9
摘要
Abstract Ga-doped Li 7 La 3 Zr 2 O 12 (Ga-LLZO) has long been considered as a promising garnet-type electrolyte candidate for all-solid-state lithium metal batteries (ASSLBs) due to its high room temperature ionic conductivity. However, the typical synthesis of Ga-LLZO is usually accompanied by the formation of undesired LiGaO 2 impurity phase that causes severe instability of the electrolyte in contact with molten Li metal during half/full cell assembly. In this study, we show that by simply engineering the defect chemistry of Ga-LLZO, namely, the lithium deficiency level, LiGaO 2 impurity phase is effectively inhibited in the final synthetic product. Consequently, defect chemistry engineered Ga-LLZO exhibits excellent electrochemical stability against lithium metal, while its high room temperature ionic conductivity (∼ 1.9 × 10 −3 S⋅cm −1 ) is well reserved. The assembled Li/Ga-LLZO/Li symmetric cell has a superior critical current density of 0.9 mA⋅cm −2 , and cycles stably for 500 hours at a current density of 0.3 mA⋅cm −2 . This research facilitates the potential commercial applications of high performance Ga-LLZO solid electrolytes in ASSLBs.
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