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Register a new userMagnetism in the high-Tc analogue Cs2AgF4 studied with muon-spin relaxation
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We present the results of a muon-spin relaxation study of the high-Tc analogue material Cs2AgF4. We find unambiguous evidence for magnetic order, intrinsic to the material, below T_C=13.95(3) K. The ratio of inter- to intraplane coupling is estimated to be |J/J|=1.9 x 10^-2, while fits of the temperature dependence of the order parameter reveal a critical exponent beta=0.292(3), implying an intermediate character between pure two- and three- dimensional magnetism in the critical regime. Above T_C we observe a signal characteristic of dipolar interactions due to linear F-mu-F bonds, allowing the muon stopping sites in this compound to be characterized.
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We present the results of muon-spin relaxation (muSR) measurements on the hexagonal manganite HoMnO3. Features in the temperature-dependent relaxation rate, lambda, correlate with the magnetic transitions at 76 K, 38 K and 34 K. The highest temperature transition, associated with the ordering of Mn3+ moments has the largest effect on lambda. The application of a static electric field of E=10^4 Vm^-1 below T=50 K causes a small reduction in lambda which is suggestive of coupling between ferroelectric and magnetic domain walls in the ordered state of the material.
We present longitudinal field muon spin relaxation ($mu$SR) measurements in the unilluminated state of the photo-sensitive molecular magnetic Co-Fe Prussian blue analogues M$_{1-2x}$Co$_{1+x}$[Fe(CN)$_6$]$cdot z$ H$_2$O, where M=K and Rb with $x=0.4$ and $simeq 0.17$, respectively. These results are compared to those obtained in the $x=0.5$ stoichiometric limit, Co$_{1.5}$[Fe(CN)$_6$]$cdot 6$ H$_2$O, which is not photo-sensitive. We find evidence for correlation between the range of magnetic ordering and the value of $x$ in the unilluminated state which can be explained using a site percolation model.
We demonstrate that quantum-critical spin dynamics can be probed in high magnetic fields using muon-spin relaxation ($mu^{+}$SR). Our model system is the strong-leg spin ladder bis(2,3-dimethylpyridinium) tetrabromocuprate (DIMPY). In the gapless Tomonaga-Luttinger liquid phase we observe finite-temperature scaling of the $mu^{+}$SR $1/T_1$ relaxation rate which allows us to determine the Luttinger parameter $K$. We discuss the benefits and limitations of local probes compared with inelastic neutron scattering.
Although the precise mechanism of high-Tc superconductivity in the layered cuprates remains unknown, it is generally thought that strong 2D Heisenberg antiferromagnetism combined with disruptive hole doping is an essential aspect of the phenomenon. Intensive studies of other layered 3d transition metal systems have greatly extended our understanding of strongly correlated electron states, but to date have failed to show strong 2D antiferromagnetism or high-Tc superconductivity. For this reason the largely unexplored 4d^9 Ag^II fluorides, which are structurally and perhaps magnetically similar to the 3d^9 Cu^II cuprates, merit close study. Here we present a comprehensive study of magnetism in the layered Ag^II fluoride Cs_2AgF_4, using magnetic susceptometry, neutron diffraction and inelastic neutron scattering techniques. We find that this material is well described as a 2D Heisenberg ferromagnet, in sharp contrast to the high-Tc cuprates. The exchange constant J is the largest known for any material of this type. We suggest that orbital ordering may be the origin of the ferromagnetism we observe in this material.
We review examples of muon-spin relaxation measurements on molecule-based magnetic coordination polymers, classified by their magnetic dimensionality. These include the one-dimensional s=1/2 spin chain Cu(pyz)(NO3)2 and the two-dimensional s=1/2 layered material [Cu(HF2)(pyz)2]BF4. We also describe some of the more exotic ground states that may become accessible in the future given the ability to tune the interaction strengths of our materials through crystal engineering.
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