Julien M-H, de Vaulx C, Mayaffre H, Berthier C, Horvatić M, Simonet V, Wooldridge J, Balakrishnan G, Lees M R, Chen D P, Lin C T, Lejay P
Laboratoire de Spectrométrie Physique, UMR5588 CNRS, 38402 Saint Martin d'Hères, France.
Phys Rev Lett. 2008 Mar 7;100(9):096405. doi: 10.1103/PhysRevLett.100.096405. Epub 2008 Mar 5.
From 59Co and 23Na NMR, we demonstrate the impact of the Na+ vacancy ordering on the cobalt electronic states in Na0.75CoO2: at long time scales, there is neither a disproportionation into 75% Co3+ and 25% Co4+ states, nor a mixed-valence metal with a uniform Co3.25+ state. Instead, the system adopts an intermediate configuration in which 30% of the lattice sites form an ordered pattern of localized Co3+ states. Above 180 K, an anomalous mobility of specific Na+ sites is found to coexist with this electronic texture, suggesting that the formation of the latter may contribute to stabilizing the Na+ ordering. Control of the ion doping in these materials thus appears to be crucial for fine-tuning of their thermoelectric properties.
通过59Co和23Na核磁共振,我们证明了Na+空位有序化对Na0.75CoO2中钴电子态的影响:在长时间尺度下,既没有歧化为75%的Co3+和25%的Co4+态,也没有具有均匀Co3.25+态的混合价金属。相反,该体系采用了一种中间构型,其中30%的晶格位点形成了局域Co3+态的有序图案。在180 K以上,发现特定Na+位点的异常迁移率与这种电子结构共存,这表明后者的形成可能有助于稳定Na+有序化。因此,控制这些材料中的离子掺杂对于微调其热电性能似乎至关重要。