Universal geometric frustration in pyrochlores.

Materials with the pyrochlore/fluorite structure have diverse technological applications, from magnetism to nuclear waste disposal. Here we report the observation of structural instability present in the pyrochlores A2Zr2O6O' (A = Pr, La) and Yb2Ti2O6O', that exists despite ideal stoichiometry, ideal cation-ordering, the absence of lone pair effects, and a lack of magnetic order. Though these materials appear to have good long-range order, local structure probes find displacements, of the order of 0.01 nm, within the pyrochlore framework. The pattern of displacements of the A2O' sublattice mimics the entropically-driven fluxional motions characteristic of and well-known in the silica mineral ß-cristobalite. The universality of such displacements within the pyrochlore structure adds to the known structural diversity and explains the extreme sensitivity to composition found in quantum spin ices and the lack of ferroelectric behavior in pyrochlores.

Reentrant Phase Diagram of Yb_{2}Ti_{2}O_{7} in a ⟨111⟩ Magnetic Field.

We present a magnetic phase diagram of rare-earth pyrochlore Yb_{2}Ti_{2}O_{7} in a ⟨111⟩ magnetic field. Using heat capacity, magnetization, and neutron scattering data, we show an unusual field dependence of a first-order phase boundary, wherein a small applied field increases the ordering temperature. The zero-field ground state has ferromagnetic domains, while the spins polarize along ⟨111⟩ above 0.65 T. A classical Monte Carlo analysis of published Hamiltonians does account for the critical field in the low T limit. However, this analysis fails to account for the large bulge in the reentrant phase diagram, suggesting that either long-range interactions or quantum fluctuations govern low field properties.

Evidence for topologically protected surface states and a superconducting phase in [Tl4](Tl(1-x)Sn(x))Te3 using photoemission, specific heat, and magnetization measurements, and density functional theory.

We report the discovery of surface states in the perovskite superconductor [Tl4]TlTe3 (Tl5Te3) and its nonsuperconducting tin-doped derivative [Tl4](Tl0.4Sn0.6)Te3 as observed by angle-resolved photoemission spectroscopy. Density functional theory calculations predict that the surface states are protected by a Z2 topology of the bulk band structure. Specific heat and magnetization measurements show that Tl5Te3 has a superconducting volume fraction in excess of 95%. Thus Tl5Te3 is an ideal material in which to study the interplay of bulk band topology and superconductivity.