中子衍射
偏心因子
晶体结构
结晶学
衍射
材料科学
粉末衍射
快离子导体
空间组
X射线晶体学
单晶
化学
电解质
物理
物理化学
光学
电极
作者
Reinhard Wagner,Günther J. Redhammer,Daniel Rettenwander,Gerold Tippelt,Andreas Welzl,Stefanie Taibl,Jürgen Fleig,Alexandra Franz,Werner Lottermoser,Georg Amthauer
标识
DOI:10.1021/acs.chemmater.6b02516
摘要
Fast Li-ion-conducting Li oxide garnets receive a great deal of attention as they are suitable candidates for solid-state Li electrolytes. It was recently shown that Ga-stabilized Li7La3Zr2O12 crystallizes in the acentric cubic space group I4̅3d. This structure can be derived by a symmetry reduction of the garnet-type Ia3̅d structure, which is the most commonly found space group of Li oxide garnets and garnets in general. In this study, single-crystal X-ray diffraction confirms the presence of space group I4̅3d also for Li7-3x Fe x La3Zr2O12. The crystal structure was characterized by X-ray powder diffraction, single-crystal X-ray diffraction, neutron powder diffraction, and Mößbauer spectroscopy. The crystal-chemical behavior of Fe3+ in Li7La3Zr2O12 is very similar to that of Ga3+. The symmetry reduction seems to be initiated by the ordering of Fe3+ onto the tetrahedral Li1 (12a) site of space group I4̅3d. Electrochemical impedance spectroscopy measurements showed a Li-ion bulk conductivity of up to 1.38 × 10-3 S cm-1 at room temperature, which is among the highest values reported for this group of materials.
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