Spin-locking effect in the nanoscale ordered perovskite cobaltite LaBaCo2O6

A new nanoscale ordered perovskite cobaltite, which consists of 90 degree ordered domains of the layered-112 LaBaCo2O6 has been evidenced by high resolution- transmission electron microscopy. This new form, like the disordered La0.5Ba0.5CoO3 and ordered LaBaCo2O6, exhibits a ferromagnetic transition at TC around 179 K. However, it differs from the two previous forms by its strong magnetic anisotropy, and correlatively by its high value of coercivity (0.42 Tesla) at low temperature. We suggest that this behaviour originates from the locking of magnetic spins in the 90 degree oriented nano-domain. Moreover, one observes a semi-metal/semi-metal transition at TC with a maximum magnetoresistance of 6.5 % at this temperature.Comment: 16 pages including figure

Electron transport and thermoelectric properties of layered perovskite LaBaCo2O5.5

We have investigated the systematic transport properties of the layered 112-type cobaltite LaBaCo2O5.5 by means of electrical resistivity, magnetoresistance, electroresistance and thermoelectric measurements in various conditions. In order to understand the complex conduction mechanism of LaBaCo2O5.5, the transport data have been analyzed using different theoretical models. The system shows semiconductor-semiconductor like transition (TSC) around 326K, corresponding to ferromagnetic transition and in the low temperature region resistivity data follows the Motts variable range hopping model. Interestingly, near and below the room temperature this compound depicts significant change in electro- and magnetoresistance behavior, the latter one is noteworthy near the magnetic phase boundary. The temperature dependence of thermopower, S(T), exhibits p-type polaronic conductivity in the temperature range of 60-320K and reaches a maximum value of 303 uV/K (at 120K). In the low temperature AFM region, the unusual S(T) behavior, generally observed for the cobaltite series LnBaCo2O5.5 (Ln = Rare Earth), is explained by the electron magnon scattering mechanism as previously described for perovskite manganites.Comment: 18 pages including fig

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 different from 0 and a crossover to a Fermi-liquid regime occurs below a characteristic temperature T*~7 K. Despite some uncertainty over the exact cobalt oxidation state n 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.Comment: 4 pages, submitte

Gallium Substituted "114" YBaFe4O7: From a ferrimagnetic cluster glass to a cationic disordered spin glass

The study of the ferrites YBaFe4-xGaxO7 shows that the substitution of Ga for Fe in YBaFe4O7 stabilizes the hexagonal symmetry for 0.40 < x < 0.70, at the expense of the cubic one. Using combined measurements of a. c. and d. c. magnetization, we establish that Ga substitution for Fe in YBaFe4O7 leads to an evolution from a geometrically frustrated spin glass (for x = 0) to a cationic disorder induced spin glass (x = 0.70). We also find an intermediate narrow range of doping where the samples are clearly phase separated having small ferrimagnetic clusters embedded in a spin glass matrix. The origin of the ferrimagnetic clusters lies in the change in symmetry of the samples from cubic to hexagonal (and a consequent lifting of the geometrical frustration) as a result of Ga doping. We also show the presence of exchange bias and domain wall pinning in these samples. The cause of both these effects can be traced back to the inherent phase separation present in the samples.Comment: 25 pages, 10 figure

Enhancement of ferromagnetism by nickel doping in the 112 cobaltite EuBaCo2O5.50

The study of the ordered oxygen deficient perovskite EuBaCo2-xNixO5.50 shows that the doping of cobalt sites by nickel induces a strong ferromagnetic component at low temperature in the antiferromagnetic matrix of EuBaCo2O5.50. This system exhibits indeed phase separation, i.e. consists of ferromagnetic domains embedded in the antiferromagnetic matrix of EuBaCo2O5.50. Besides, a magnetic transition is observed for the first time at 40K in the undoped and nickel doped phases, which can be attributed to the ferromagnetic ordering of the Eu3+ moments below this temperature. Moreover sharp ultra magnetization multisteps are observed below 5K, characteristic of motion of domain walls in a strong pinning system and very different from any metamagnetic transition

Competition between ferromagnetism and spin glass: the key for large magnetoresistance in oxygen deficient perovskites SrCo1-xMxO3-d (M = Nb, Ru)

The magnetic and magnetotransport properties of the oxygen deficient perovskites, SrCo1-xMxO3-d with M = Nb and Ru, were investigated. Both Nb- and Ru-substituted cobaltites are weak ferromagnets, with transition temperatures Tm of 130-150 K and 130-180 K, respectively, and both exhibit a spin glass behavior at temperatures below Tf = 80-90 K. It is demonstrated that there exists a strong competition between ferromagnetism and spin glass state, where Co4+ induces ferromagnetism, whereas Nb or Ru substitution at the cobalt sites induces magnetic disorder, and this particular magnetic behavior is the origin of large negative magnetoresistance of these oxides, reaching up to 30% at 5 K in 7 T. The differences between Nb- and Ru-substituted cobaltites are discussed on the basis of the different electronic configuration of niobium and ruthenium cations.Comment: 32 pages, 9 figures, to appear in Phys. Rev.