23Na NMR evidence for charge order and anomalous magnetism in NaxCoO2

Oriented powder samples of NaxCoO2 are studied by 23Na NMR and SQUID magnetometry. In nominal 0.50相似文献   

Metamagnetic transition in Na 0.85 CoO2 single crystals

We report the magnetization, specific heat, and transport measurements of a high quality Na(0.85)CoO2 single crystal in applied magnetic fields up to 14 T. At high temperatures, the system is in a paramagnetic phase. It undergoes a magnetic phase transition below approximately 20 K. For the field H||c, the measurement data of magnetization, specific heat, and magnetoresistance reveal a metamagnetic transition from an antiferromagnetic state to a quasiferromagnetic state at about 8 T at low temperatures. However, no transition is observed in the magnetization measurements up to 14 T for H perpendicular c. The low temperature magnetic phase diagram of Na(0.85)CoO2 is determined.     

Angle-resolved photoemission study of the cobalt oxide superconductor Na(x)CoO(2) x yH(2)O: observation of the Fermi surface

The cobalt oxide superconductor Na(x)CoO(2) x yH(2)O is studied by angle-resolved photoemission spectroscopy. We report the Fermi surface (FS) topology and electronic structure near the Fermi level (E(F)) in the normal state of Na(x)CoO(2) x yH(2)O. Our result indicates the presence of the hexagonal FS centered at the Gamma point, while the small pocket FSs along Gamma-K direction are absent, similar to Na(x)CoO(2). The top of the e(g)(') band, which is expected in band calculations to form the small pocket FSs, extends to within approximately 30 meV below E(F), closer to E(F) than in Na(x)CoO(2). We discuss its possible role in superconductivity, comparing with other experimental and theoretical results.     

Direct link between low-temperature magnetism and high-temperature sodium order in NaxCoO2

We prove the direct link between low-temperature (T) magnetism and high-T Na+ ordering in NaxCoO2 using the example of a so far unreported magnetic transition at 8 K which involves a weak ferromagnetic moment. The 8 K feature is characterized in detail and its dependence on a diffusive Na+ rearrangement around 200 K is demonstrated. Applying muons as local probes this process is shown to result in a reversible phase separation into distinct magnetic phases that can be controlled by specific cooling protocols. Thus the impact of ordered Na+ Coulomb potential on the CoO2 physics is evidenced opening new ways to experimentally revisit the NaxCoO2 phase diagram.     

Determination of the Co valence in bilayer hydrated superconducting NaxCoO2 · yH2O by soft x-ray absorption spectroscopy

We addressed the so-far unresolved issue concerning the Co valence in the superconducting bilayer hydrated Na(x)CoO(2) · yH(2)O (x～0.35, y～1.3) using soft x-ray absorption spectroscopy at the Co-L(2,3) and O-K edges. We find that the valence state of the Co lies in a narrow range from +3.3 to +3.4 for all studied Na(x)CoO(2) · yH(2)O samples and their deuterated analogue with T(c)'s ranging from 3.8 to 4.7 K. These valence values are far from the often claimed +3.7, the number based on the Na content only. We propose to modify the phase diagram accordingly, where the basic electronic structure of the superconducting phase is very close to that of the Na(0.7)CoO(2) system, suggesting that the presence of in-plane spin fluctuations could play an important role for the superconductivity.     

Electronic model for CoO2 layer based systems: chiral resonating valence bond metal and superconductivity

Takada et al. have reported superconductivity in layered Na(x)CoO(2)yH(2)O (T(c) approximately equal to 5 K). We model a reference neutral CoO2 layer as an orbitally nondegenerate spin-1/2 antiferromagnetic Mott insulator on a triangular lattice and Na(x)CoO(2)yH(2)O as electron doped Mott insulators described by a t-J model. It is suggested that at optimal doping chiral spin fluctuations enhanced by the dopant dynamics lead to a gapful d-wave superconducting state. A chiral resonating valence bond (RVB) metal, a parity and time (PT) reversal violating state with condensed RVB gauge fields, with a possible weak ferromagnetism, and low temperature p-wave superconductivity are also suggested at higher dopings.     

17O NMR studies of a triangular-lattice superconductor NaxCoO2 x yH(2)O

We report the first 17O NMR studies of a triangular-lattice superconductor Na(1/3)CoO2 x 4/3H(2)O and the host material Na(x)CoO2 (x=0.35 and 0.72). Knight shift measurements reveal that p-d hybridization induces sizable spin polarization in the O triangular-lattice layers. Water intercalation makes CoO2 planes homogeneous and enhances low frequency spin fluctuations near T(c)=4.5 K at some finite wave vectors different from both the ferromagnetic and "120 degree" modes.     

Fermi surface of NaxCoO2

Doping evolution of the Fermi surface topology of Na(x)CoO(2) is studied systematically. Both local density approximation (LDA) and local spin density approximation (LSDA) predict a large Fermi surface as well as small hole pockets for doping levels x approximately 0.5. In contrast, the hole pockets are completely absent for all doping levels within LSDA+U. More importantly, we find no violation of Luttinger's rule in this system. The measured Fermi surface of Na(0.7)CoO(2) can be explained by its half-metallic behavior and agrees with our LSDA+U calculations.     

Three-dimensional spin fluctuations in Na0.75CoO2

We report polarized- and unpolarized-neutron scattering measurements of magnetic excitations in single-crystal Na0.75CoO2. The data confirm ferromagnetic correlations within the cobalt layers and reveal antiferromagnetic correlations perpendicular to the layers, consistent with an A-type antiferromagnetic ordering. The magnetic modes propagating perpendicular to the layers are sharp, and reach a maximum energy of approximately 12 meV. From a minimal spin-wave model, containing only nearest-neighbor Heisenberg exchange interactions, we estimate the interlayer and intralayer exchange constants to be 12.2+/-0.5 meV and -6+/-2 meV, respectively. We conclude that the magnetic fluctuations in Na0.75CoO2 are highly three dimensional.     

59Co NMR evidence for charge ordering below T_(CO) approximately 51 K in Na0.5CoO2

The CoO2 layers in NaxCoO2 may be viewed as a spin S=1/2 triangular-lattice doped with charge carriers. The underlying physics of the cobaltates is very similar to that of the high T_(c) cuprates. We will present unequivocal 59Co NMR evidence that below T_(CO) approximately 51 K, the insulating ground state of the itinerant antiferromagnet Na0.5CoO2 (T_(N) approximately 86 K) is induced by charge ordering.     

Neutron scattering study of novel magnetic order in Na0.5CoO2

We report polarized and unpolarized neutron scattering measurements of the magnetic order in single crystals of Na0.5CoO2. Our data indicate that below TN=88 K the spins form a novel antiferromagnetic pattern within the CoO2 planes, consisting of alternating rows of ordered and nonordered Co ions. The domains of magnetic order appear to be closely coupled to the domains of Na ion order, consistent with such a twofold symmetric spin arrangement. Magnetoresistance and anisotropic susceptibility measurements further support this model for the electronic ground state.     

Electronic correlations in CoO2, the parent compound of triangular cobaltates

A 59Co NMR study of CoO2, the x=0 end member of AxCoO2 (A=Na,Li,...) cobaltates, reveals a metallic ground state, though with clear signs of strong electron correlations: low-energy spin fluctuations develop at wave vectors q not equal to 0 and a crossover to a Fermi-liquid regime occurs below a characteristic temperature T* approximately 7 K. Despite some uncertainty over the exact cobalt oxidation state in this material, the results show that electronic correlations are revealed as x is reduced below 0.3. The data are consistent with NaxCoO2 being close to the Mott transition in the x-->0 limit.     

Magnetic ordering and spin waves in Na0.82CoO2

NaxCoO2, the parent compound of the recently synthesized superconductor Na(x)CoO(2):yH(2)O, exhibits bulk antiferromagnetic order below approximately 20 K for 0.75相似文献   

Infrared spectroscopy of the charge ordering transition of Na0.5CoO2

We report infrared reflectivity study of charge ordering in a Na0.5CoO2 single crystal. In comparison with x=0.7 and 0.85 compounds, we found that the effective carrier density increases systematically with decreasing Na contents. The charge ordering transition only affects the optical spectra below 1000 cm(-1). A hump near 800 cm(-1) develops below 100 K, which is accompanied by the appearance of new lattice modes as well as the strong antiresonance feature of phonon spectra. These observations signify a polaronic characteristic of charge carriers. Below T(co), an optical gap develops at the magnitude of 2Delta approximately 3.5k(B)T(co) (T相似文献   

NMR study of the magnetic and metal-insulator transitions in Na0.5CoO2: a nesting scenario

Co and Na NMR are used to probe the local susceptibility and charge state of the two Co sites of the Na-ordered orthorhombic Na(0.5)CoO(2). Above T(N) = 86 K, both sites display a similar T dependence of the spin shift, suggesting that there is no charge segregation into Co(3+) and Co(4+) sites. Below T(N), the magnetic long range commensurate order found is only slightly affected by the metal-insulator transition at T(MIT) = 51 K. Furthermore, the electric field gradient at the Co site does not change at these transitions, indicating the absence of charge ordering. All these observations can be explained by successive spin-density wave induced by two nestings of the Fermi surface specific to the x = 0.5 Na ordering.     

Percolation and the colossal magnetoresistance of Eu-based hexaboride

Upon substituting Ca for Eu in the local-moment ferromagnet EuB6, the Curie temperature T(C) decreases substantially with increasing dilution of the magnetic sublattice and is completely suppressed for x相似文献   

Fermi surface evolution and Luttinger theorem in Na(x)CoO2: a systematic photoemission study

We report a systematic angle-resolved photoemission study on Na(x)CoO2 for a wide range of Na concentrations (0.3 < or = x < or = 0.72). In all the metallic samples at different x, we observed (i) only a single holelike Fermi surface centered around gamma and (ii) its area changes with x according to the Luttinger theorem. We also observed a surface state that exhibits a larger Fermi surface area. The e'(g) band and the associated small Fermi surface pockets near the K points predicted by band calculations are found to sink below the Fermi energy in a manner almost independent of the doping and temperature.     

Shubnikov-de Haas effect in the metallic state of Na0.3CoO2

Shubnikov-de Haas oscillations for two well-defined frequencies, corresponding, respectively, to areas of 0.8 and 1.36% of the first Brillouin zone, were observed in single crystals of Na(0.3)CoO2. The existence of Na superstructures in Na0.3CoO2, coupled with this observation, suggests the possibility that the periods are due to the reconstruction of the large Fermi surface around the Gamma point. An alternative interpretation in terms of the long sought-after epsilon'(g) pockets is also considered but found to be incompatible with existing specific heat data.     

Er1-xDyxNi2B2C体系中超导和磁性的共存和相互作用

本在2K～20K温区内系统地研究了Er1-xDyxNi2B2C体系中超导转变温度Tc的反铁磁转变温度TN随Dy掺杂含量x的变化．实验发现x=0．3和x=0．8附近的样品具有复杂的磁结构．这些洋品有两个磁转变温度(TN’和TN)．对于该体系发现了两个主要的特征：1)在x=0．3附近，超导被抑制，TN’出现一个小的峰值；2)在x=0．8附近，Tc出现一个低谷，TN’出现一个大的宽峰．TN’在x=0．3和x=0．8附近的异常来源于改系统中超导和磁性的共存和相互作用。     

Spin-glass-like behavior in CoO nanoparticles and the origin of exchange bias in layered CoO/ferromagnet structures

The magnetic behavior of CoO nanoparticles and layered CoO/ferromagnetic (FM) structures has been investigated by magnetization and hysteresis loop measurements. In the amorphous CoO, a large uncompensation of spins is found that is closely related to spin-glass-like behavior below a freezing temperature T(F) approximately 215-220 K. The spin-glass-like phase may be described by the de Almeida-Thouless line for Ising spin systems. The exchange bias in the layered CoO/FM structures is explained by the spin-glass-like state in the nanoparticles constituting the CoO film.