锂(药物)
离子键合
硼氢化
接口(物质)
硼氢化钠
材料科学
化学
化学工程
离子
无机化学
化学物理
吸附
心理学
物理化学
工程类
有机化学
催化作用
吉布斯等温线
精神科
作者
Yijiao Wang,Peng Liu,Shuo Wang,Xin Zhan,Miao Yu,Cai-Ting Yuan,Pingting He,Yingtong Lv,Tengfei Zhang
标识
DOI:10.1002/adsu.202400428
摘要
Abstract Garnetbased all‐solid‐state electrolytes are promising because of their wide electrochemical window and high ionic conductivity. However, the preparation process for garnet‐based solid‐state electrolytes is complex, requiring a high sintering temperature (>1050 °C) and a long sintering time (>10 h), which results in poor contact with the electrode. In this work, hydride coating modification can effectively improve the interface contact of oxide particles and enhance the ability of ion conduction. Hence, a series of composite electrolytes Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 ‐xwt%Li(NH 3 ) 0.2 BH 4 (LLZTO‐xwt%LNB, 0≤x≤30) is synthesized at Room temperature (RT), in which hydrides uniformly coat and fill in the pores of LLZTO to provide lithium‐ion transport channels. At 30 °C, the conductivity of LLZTO‐10wt%Li(NH 3 ) 0.2 BH 4 (LLZTO‐10wt%LNB, 2.3 × 10 −4 S cm −1 ) is four orders higher than pristine untreated LLZTO (8.7 × 10 −8 S cm −1 ), and two orders higher than pristine Li(NH 3 ) 0.2 BH 4 (1.3 × 10 −6 S cm −1 ). The critical current density reaches up to 3 mA cm −2 , demonstrating excellent stability against lithium. These strategies positively impact the development and application of solid‐state electrolytes.
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