材料科学
离子电导率
电解质
电导率
锂(药物)
陶瓷
化学工程
快离子导体
阳极
离子键合
无机化学
复合材料
离子
物理化学
电极
化学
有机化学
工程类
内分泌学
医学
作者
Yu Liu,Hongling Peng,Han Su,Yu Zhong,Xiuli Wang,Xinhui Xia,Changdong Gu,J.P. Tu
标识
DOI:10.1002/adma.202107346
摘要
Lithium argyrodites are one of the most promising sulfide electrolytes due to their high ionic conductivity and ductile feature. Among them, Li6 PS5 I (LPSI) exhibits better stability against Li metal but a rather low ionic conductivity (only ≈10-6 S cm-1 ) because of the absence of S2- /I- disorder. Herein, argyrodite Li6-x PS5-x I1+x glass-ceramic electrolytes with high iodine content are synthesized using ultimate-energy mechanical alloying method. S2- /I- disorder is successfully introduced into the system by doping LiI during this one-pot process. Determined by 6 Li magic angle spinning nuclear magnetic resonance and ab initio molecular dynamics simulations, the introduction of iodine promotes Li+ inter-cage jumps, leading to an enhanced long-range Li+ conducting. The Li5.6 PS4.6 I1.4 glass-ceramic electrolyte (LPSI1.4 -gc) possesses high ionic conductivity (2.04 mS cm-1 ) and excellent stability against Li metal. The Li symmetric cell with the LPSI1.4 -gc electrolyte demonstrates ultralong cycling stability over 3200 h at 0.2 mA cm-2 . LiCoO2 /Li6 PS5 Cl/Li all-solid-state battery applying LPSI1.4 -gc as the anode interlayer also presents prominent cycling and rate performance. This work provides a novel type of electrolyte with high ionic conductivity and stability against Li metal.
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