Advanced Institute for Materials Research, Tohoku University, Sendai 980-8577, Japan and Center for Emergent Matter Science, RIKEN, Wako, Saitama 351-0198, Japan.
Phys Rev Lett. 2013 Sep 20;111(12):126104. doi: 10.1103/PhysRevLett.111.126104. Epub 2013 Sep 18.
Li(x)CoO(2) exhibits intriguing electronic properties due to a strong electron correlation and complex interplay between Co and Li ions. However, fundamental understanding of the nanoscale distribution of Li ions and its effect on the electronic properties remains unclear. We use scanning tunneling microscopy and density functional theory to elucidate the degree of Li(x)CoO(2) surface electronic state modification that can be achieved by Li ordering. The surface Li ions are highly mobile and preferentially form a (1 × 1) hexagonal lattice, whereas the surface CoO(2) layer shows metallic and insulating phases, indicating the coexistence of ordered and disordered Li ions in the subsurface layer. These results provide evidence of novel electronic properties produced by spatially inhomogeneous Li-ordering patterns.
Li(x)CoO(2) 由于强电子相关和 Co 与 Li 离子的复杂相互作用,表现出有趣的电子特性。然而,对于 Li 离子的纳米级分布及其对电子特性的影响的基本理解仍不清楚。我们使用扫描隧道显微镜和密度泛函理论来阐明 Li 有序化可以实现 Li(x)CoO(2) 表面电子态修饰的程度。表面 Li 离子具有高迁移率,优先形成(1 × 1)六方晶格,而表面 CoO(2)层表现出金属和绝缘相,表明亚表层中存在有序和无序 Li 离子的共存。这些结果提供了由空间不均匀 Li 有序模式产生的新型电子特性的证据。