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تسجيل مستخدم جديدPatterning of sodium ions and the control of electrons in sodium cobaltate
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NaxCoO2 has emerged as a material of exceptional scientific interest due to the potential for thermoelectric applications, and because the strong interplay between the magnetic and superconducting properties has led to close comparisons with the physics of the high-Tc cuprates. The density, x, of the sodium in the intercalation layers can be altered electrochemically, directly changing the number of conduction electrons on triangular Co layers. Recent electron diffraction measurements reveal a kaleidoscope of Na+ ion patterns as a function of concentration. Here we use single-crystal neutron diffraction supported by numerical simulations to determine the long-range three-dimensional superstructures of these ions. We show that the sodium ordering and its associated distortion field are governed by pure electrostatics, and the organizational principle is the stabilization of charge droplets that order long range at some simple fractional fillings. Our results provide a good starting point to understand the electronic properties in terms of a Hubbard Hamiltonian taking into account the electrostatic potential from the Na superstructures. The resulting depth of potential wells in the Co layer is greater than the single-particle hopping kinetic energy. As a consequence, holes occupy preferentially the lowest potential regions and, therefore, the Na+ ion patterning plays a decisive role in the transport and magnetic properties.
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We have grown single crystals of Na$_x$Ca$_y$CoO$_2$ and determined their superstructures as a function of composition using neutron and x-ray diffraction. Inclusion of Ca$^{2+}$ stabilises a single superstructure across a wide range of temperatures
and concentrations. The superstructure in the Na$^+$ layers is based on arrays of divacancy clusters with Ca$^{2+}$ ions occupying the central site, and it has an ideal concentration Na$_{4/7}$Ca$_{1/7}$CoO$_2$. Previous measurements of the thermoelectric properties on this system are discussed in light of this superstructure. Na$_{4/7}$Ca$_{1/7}$CoO$_2$ corresponds to the maximum in thermoelectric performance of this system.
The sodium reordering in NaxCoO2 in the vicinity of room temperature is rationalized at high x in terms of phase transitions between square and striped phases. A striking hexagon-of-hexagons diffraction pattern observed for x=0.78 can be reproduced u
sing coexisting square and striped phases that are related by simple shear deformations. All compositions exhibit a partial melting transition to a disordered stripe phase just below room temperature, which alters the topology of the electrical conduction pathways.
In this study, we synthesized single crystals of Na$_{x}$CoO$_{2}$ with $xsim0.8$ using the optical floating zone technique. A thorough electrochemical treatment of the samples permitted us to control the de-intercalation of Na to obtain single cryst
al samples of stable Na ordered phases with $x=0.5-0.8$. Comparisons of the bulk magnetic properties with those observed in the Na ordered powder samples confirmed the high quality of these single crystal phases. The ab plane resistivity was measured for the Na ordered samples and it was quite reproducible for different sample batches. The data were analogous to those found in previous initial experimental studies on single crystals, but the lower residual resistivity and sharper anti-ferromagnetic transitions determined for our samples confirmed their higher quality.
Neutron and x-ray powder diffraction have been used to investigate the crystal structures of a sample of the newly-discovered superconducting sodium cobaltate deuterate compound with composition Na0.31(3)CoO2o1.25(2)D2O and its anhydrous parent compo
und Na0.61(1)CoO2. The deuterate superconducting compound is formed by coordinating four D2O molecules (two above and two below) to each Na ion in a way that gives Na-O distances nearly equal to those in the parent compound. One deuteron of the D2O molecule is hydrogen bonded to an oxygen atom in the CoO2 plane and the oxygen atom and the second deuteron of each D2O molecule lie approximately in a plane between the Na layer and the CoO2 layers. This coordination of Na by four D2O molecules leads to ordering of the Na ions and D2O molecules. The sample studied here, which has Tc=4.5 K, has a refined composition of Na0.31(3)CoO2o1.25(2)D2O, in agreement with the expected 1:4 ratio of Na to D2O. These results show that the optimal superconducting composition should be viewed as a specific hydrated compound, not a solid solution of Na and D2O (H2O) in NaxCoO2oyD2O. Studies of physical properties vs. Na or D2O composition should be viewed with caution until it is verified that the compound remains in the same phase over the composition range of the study.
Polarized Raman and optical spectra for the quasi one-dimensional metallic vanadate beta-Na0.33V2O3 are reported for various temperatures. The spectra are discussed in the light of the sodium and charge ordering transitions occurring in this material
, and demonstrate the presence of strong electron phonon coupling.
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