Kuhn Alexander, Gerbig Oliver, Zhu Changbao, Falkenberg Frank, Maier Joachim, Lotsch Bettina V
Max Planck Institute for Solid State Research, Heisenbergstr. 1, 70569 Stuttgart, Germany.
Phys Chem Chem Phys. 2014 Jul 28;16(28):14669-74. doi: 10.1039/c4cp02046d.
We report on a new ultrafast solid electrolyte of the composition Li11Si2PS12, which exhibits a higher room-temperature Li ion diffusivity than the present record holder Li10GeP2S12. We discuss the high-pressure synthesis and ion dynamics of tetragonal Li11Si2PS12, and comparison is made with our investigations of related members of the LMePS family, i.e. electrolytes of the general formula Li11-xMe2-xP1+xS12 with Me = Ge, Sn : Li10GeP2S12, Li7GePS8, Li10SnP2S12. The structure and dynamics were studied with multiple complementary techniques and the macroscopic diffusion could be traced back to fast Li ion hopping in the crystalline lattice. A clear correlation between the diffusivity and the unit cell volume of the LGPS-type electrolytes was observed.
我们报道了一种新的成分Li11Si2PS12的超快固体电解质,其在室温下的锂离子扩散率高于目前的记录保持者Li10GeP2S12。我们讨论了四方晶系Li11Si2PS12的高压合成和离子动力学,并与我们对LMePS家族相关成员的研究进行了比较,即通式为Li11-xMe2-xP1+xS12的电解质,其中Me = Ge、Sn:Li10GeP2S12、Li7GePS8、Li10SnP2S12。采用多种互补技术研究了其结构和动力学,宏观扩散可追溯到晶格中快速的锂离子跳跃。观察到LGPS型电解质的扩散率与晶胞体积之间存在明显的相关性。