Department of Chemistry, Stony Brook University, Stony Brook, New York 11794-3400, United States.
Inorg Chem. 2013 Aug 5;52(15):8540-50. doi: 10.1021/ic400579w. Epub 2013 Jul 24.
A series of layered oxides within the Na(x)Ni(ix/2)Mn(1-x/2)O2 (2/3 ≤ x ≤ 1) system were synthesized by classical solid-state methodologies. A study of their long and short-range structure was undertaken by combining X-ray diffraction and NMR spectroscopy. A transition from P2 to O3 stacking was observed at x > 0.8 when samples were made at 900 °C, which was accompanied by disordering of ions in the transition metal layer. The magnetic properties of the materials were consistent with this picture of ordering, with all samples showing antiferromagnetic character. At x = 2/3, competition between a P2 and a P3 structure, with different degrees of transition metal ordering, was found depending on the synthesis temperature. Na/Li exchange led to structures with octahedral or tetrahedral coordination of the alkali metal, and Li/Ni crystallographic exchange in the resulting O3 phases. The transition from alkali metal prismatic coordination to octahedral/tetrahedral coordination involves [TMO6]∞ layer shearing that induces some structural disorder through the formation of stacking faults.
通过经典的固态方法合成了一系列位于 Na(x)Ni(ix/2)Mn(1-x/2)O2(2/3 ≤ x ≤ 1)系统中的分层氧化物。通过结合 X 射线衍射和 NMR 光谱研究了它们的长程和短程结构。当在 900°C 下合成时,当 x > 0.8 时,观察到从 P2 到 O3 堆叠的转变,这伴随着过渡金属层中离子的无序化。材料的磁性性质与这种有序性一致,所有样品均表现出反铁磁性。在 x = 2/3 时,取决于合成温度,发现存在 P2 和 P3 结构之间的竞争,它们具有不同程度的过渡金属有序化。Na/Li 交换导致具有八面体或四面体配位的碱金属和 O3 相中 Li/Ni 晶体学交换的结构。从碱金属棱柱配位到八面体/四面体配位的转变涉及[TMO6]∞层的剪切,通过形成堆垛层错诱导一些结构无序。