Roudebush John H, Ross K A, Cava R J
Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.
Dalton Trans. 2016 Jun 7;45(21):8783-9. doi: 10.1039/c6dt00798h. Epub 2016 May 5.
We report the structure and magnetic properties of two new iridium-based honeycomb Delafossite compounds, Cu3NaIr2O6 and Cu3LiIr2O6, formed by a topotactic cation exchange reaction. The starting materials Na2IrO3 and Li2IrO3, which are based on layers of IrO6 octahedra in a honeycomb lattice separated by layers of alkali ions, are transformed to the title compounds by a topotactic exchange reaction through heating with CuCl below 450 °C; higher temperature reactions cause decomposition. The new compounds display dramatically different magnetic behavior from their parent compounds - Cu3NaIr2O6 has a ferromagnetic like magnetic transition at 10 K, while Cu3LiIr2O6 retains the antiferromagnetic transition temperature of its parent compound but displays significantly stronger dominance of antiferromagnetic coupling between spins. These results reveal that a surprising difference in the magnetic interactions between the magnetic Ir ions has been induced by a change in the non-magnetic interlayer species. A combination of neutron and X-ray powder diffraction is used for the structure refinement of Cu3NaIr2O6 and both compounds are compared to their parent materials.
我们报道了通过拓扑阳离子交换反应形成的两种新型铱基蜂窝状方铁矿化合物Cu3NaIr2O6和Cu3LiIr2O6的结构和磁性。起始材料Na2IrO3和Li2IrO3基于由碱离子层隔开的蜂窝晶格中的IrO6八面体层,通过在450°C以下与CuCl加热进行拓扑交换反应转化为标题化合物;更高温度的反应会导致分解。新化合物与其母体化合物表现出截然不同的磁行为——Cu3NaIr2O6在10 K时具有类似铁磁的磁转变,而Cu3LiIr2O6保留了其母体化合物的反铁磁转变温度,但显示出自旋间反铁磁耦合的显著更强优势。这些结果表明,非磁性层间物种的变化导致了磁性Ir离子之间磁相互作用的惊人差异。结合中子和X射线粉末衍射对Cu3NaIr2O6进行结构精修,并将这两种化合物与其母体材料进行比较。