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Geometrical frustration among interacting spins combined with strong quantum fluctuations destabilize long-range magnetic order in favor of more exotic states such as spin liquids. By following this guiding principle, a number of spin liquid candidate systems were identified in quasi-two-dimensional (quasi-2D) systems. For 3D, however, the situation is less favorable as quantum fluctuations are reduced and competing states become more relevant. Here we report a comprehensive study of thermodynamic, magnetic and dielectric properties on single crystalline and pressed-powder samples of PbCuTe2O6, a candidate material for a 3D frustrated quantum spin liquid featuring a hyperkagome lattice. Whereas the low-temperature properties of the powder samples are consistent with the recently proposed quantum spin liquid state, an even more exotic behavior is revealed for the single crystals. These crystals show ferroelectric order at TFE ≈ 1 K, accompanied by strong lattice distortions, and a modified magnetic response—still consistent with a quantum spin liquid—but with clear indications for quantum critical behavior.
Dilatometric studies on single crystalline barlowite – a structurally perfect spin-1/2 Kagome system
(2015)
We present results of high-resolution thermal expansion measurements on single crystalline barlowite – a structurally perfect spin-1/2 kagome system. The data reveal strongly pronounced and anisotropic second-order phase transition anomalies at the Néel transition at TN = 16K. From these data, together with literature results on the specific heat, the uniaxial-pressure dependences of TN are derived. We find a rather large positive pressure coefficient for uniaxial pressure along the hexagonal c axis of ∂TN/∂pc = (2.3 ± 0.2) K/GPa and smaller negative in-plane pressure coefficient of ∂TN/∂pin-plane = -(0.6 ± 0.03) K/GPa. These effects result in a small positive pressure coefficient under hydrostatic-pressure conditions of ∂TN/∂phydr = (1.1 ± 0.2) K/GPa. Bond-lengths considerations indicate that inter-layer Cu-O bonds, being larger than those typically found in stable Cu-O complexes, are responsible for this behavior.