Cabana Jordi, Casas-Cabanas Montserrat, Omenya Fredrick O, Chernova Natasha A, Zeng Dongli, Whittingham M Stanley, Grey Clare P
Environmental Energy Technologies Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720.
Chem Mater. 2012 Aug 14;24(15):2952-2964. doi: 10.1021/cm301148d. Epub 2012 Jul 19.
A study of the correlations between the stoichiometry, secondary phases and transition metal ordering of LiNi(0.5)Mn(1.5)O(4) was undertaken by characterizing samples synthesized at different temperatures. Insight into the composition of the samples was obtained by electron microscopy, neutron diffraction and X-ray absorption spectroscopy. In turn, analysis of cationic ordering was performed by combining neutron diffraction with Li MAS NMR spectroscopy. Under the conditions chosen for the synthesis, all samples systematically showed an excess of Mn, which was compensated by the formation of a secondary rock salt phase and not via the creation of oxygen vacancies. Local deviations from the ideal 3:1 Mn:Ni ordering were found, even for samples that show the superlattice ordering by diffraction, with different disordered schemes also being possible. The magnetic behavior of the samples was correlated with the deviations from this ideal ordering arrangement. The in-depth crystal-chemical knowledge generated was employed to evaluate the influence of these parameters on the electrochemical behavior of the materials.
通过对在不同温度下合成的样品进行表征,研究了LiNi(0.5)Mn(1.5)O(4)的化学计量比、第二相和过渡金属有序化之间的相关性。通过电子显微镜、中子衍射和X射线吸收光谱对样品的组成进行了深入了解。反过来,通过将中子衍射与Li MAS NMR光谱相结合来进行阳离子有序化分析。在所选的合成条件下,所有样品都系统地显示出过量的Mn,这是通过形成次生岩盐相来补偿的,而不是通过产生氧空位来补偿。即使对于通过衍射显示出超晶格有序化的样品,也发现了与理想的3:1 Mn:Ni有序化的局部偏差,并且还可能存在不同的无序方案。样品的磁行为与偏离这种理想有序排列的情况相关。所产生的深入的晶体化学知识被用于评估这些参数对材料电化学行为的影响。