电化学
锂(药物)
电导率
材料科学
晶格常数
离子
电解质
价(化学)
电化学窗口
晶体结构
离子电导率
结晶学
分析化学(期刊)
化学
物理化学
电极
医学
物理
有机化学
色谱法
内分泌学
衍射
光学
作者
Kai Ma,Bowen Chen,Cheng‐Xin Li,Venkataraman Thangadurai
标识
DOI:10.1021/acs.jpcc.2c01380
摘要
In this work, the Mg and Nb codoped garnet-type solid electrolytes Li7+x–yLa3–xMgxZr2–yNbyO12 (0 ≤ x ≤ 0.4; 0.4 ≤ y ≤ 0.8) for all-solid-state Li-ion batteries were prepared by conventional solid-state method. The formation of a single-phase garnet structure (space group Ia3̅d) with lattice constant decreased from 12.94452(19) Å (x = 0, y = 0.4) to 12.92286(14) Å (x = 0.4, y = 0.8) have been observed. The La and Zr were substituted by Mg (24c) and Nb (16a), respectively, which greatly altered the conductivity of the sample. Additionally, a high-density structure was obtained through sintering at 1150 °C. The Mg and Nb codoped Li7La3Zr2O12 (LLZO) achieved Li-ion conductivity, ranging from 7.49 × 10–4 S·cm–1 (x = 0, y = 0.4) to 1.95 × 10–4 S·cm–1 (x = 0.4, y = 0.8) at 25 °C. The Li-ion 3D diffusion pathway was constructed by the bond valence sum mapping of Mg and Nb codoped LLZO. The Mg and Nb codoped LLZO retains remarkable electrochemical stability against lithium after 600 cycles at 0.1 mA·cm–2. This work may inspire the rational design of garnet-based electrolyte materials to attain high performance in the energy storage field.
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