Biomedical subjects

B G Ueland

Publications and source records attributed to B G Ueland.

4 recordsLinked to original sources

PubMed2006

Unconventional dynamics in triangular Heisenberg antiferromagnet NaCrO2.

We report magnetization, specific heat, muon spin rotation, and Na NMR measurements on the S=3/2 rhombohedrally stacked Heisenberg antiferromagnet NaCrO2. This compound appears to be a good candidate for the study of isotropic triangular Heisenberg antiferromagnets with very weak interlayer coupling. While specific heat and magnetization measurements indicate the onset of a transition in the range Tc approximately 40-50 K, both muon spin rotation and NMR reveal a fluctuating crossover regime extending well below Tc, with a peak of relaxation rate T1(-1) around T approximately 25 K. This novel finding is discussed within the context of excitations in the triangular Heisenberg antiferromagnets.

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PubMed2006

Slow spin relaxation in a highly polarized cooperative paramagnet.

We report measurements of the ac susceptibility of the cooperative paramagnet Tb2Ti2O7 in a strong magnetic field. Our data show the expected saturation maximum in chi(T) and also an unexpected frequency dependence of this peak at low frequencies (<1 Hz), suggesting very slow spin relaxations are occurring. Measurements on samples diluted with nonmagnetic Y3+ or Lu3+ and complementary measurements on pure and diluted Dy2Ti2O7 strongly suggest that the relaxation is associated with dipolar spin correlations, representing unusual cooperative behavior in a paramagnetic system.

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PubMed2003

Quantum-classical reentrant relaxation crossover in Dy2Ti2O7 spin ice.

We have studied spin relaxation in the spin ice compound Dy2Ti2O7 through measurements of the ac magnetic susceptibility. While the characteristic spin-relaxation time (tau) is thermally activated at high temperatures, it becomes almost temperature independent below T(cross) approximately 13 K. This behavior, combined with nonmonotonic magnetic field dependence of tau, indicates that quantum tunneling dominates the relaxational process below that temperature. As the low-entropy spin ice state develops below T(ice) approximately 4 K, tau increases sharply with decreasing temperature, suggesting the emergence of a collective degree of freedom for which thermal relaxation processes again become important as the spins become strongly correlated.

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PubMed2003

Ba2LnSbO6 and Sr2LnSbO6 (Ln = Dy, Ho, Gd) double perovskites: lanthanides in the geometrically frustrating fcc lattice.

Magnetic ground states in solids often arise as a result of a delicate balance between competing factors. One currently active area of research in magnetic materials involves compounds in which long-range magnetic ordering at low temperatures is frustrated by the geometry of the crystalline lattice, a situation known as geometrical magnetic frustration. The number of systems known to display the effects of such frustration is growing, but those that are sufficiently simple from theoretical, chemical, and physical perspectives to allow for detailed understanding remain very few. A search for model compounds in this family has led us to the double perovskites Ba2LnSbO6 and Sr2LnSbO6 (Ln = Dy, Ho, and Gd) reported here. Ba2DySbO6,Ba2HoSbO6,Sr2DySbO6, and Sr2HoSbO6 are structurally characterized by powder neutron diffraction at ambient temperature. The trivalent lanthanides and pentavalent antimony are found to be fully ordered in the double-perovskite arrangement of alternating octahedra sharing corner oxygens. In such a structure, the lanthanide sublattice displays a classical fcc arrangement, an edge-shared network of tetrahedra known to result in geometric magnetic frustration. No magnetic ordering is observed in any of these compounds down to temperatures of 2 K, and in the case of the Dy-based compounds in particular, frustration of the magnetic ordering is clearly present. Lanthanide-based double perovskites are proposed to be excellent model systems for the detailed study of geometric magnetic frustration.

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