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Register a new userTemperature dependence of quantum oscillations from non-parabolic dispersions
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The phase offset of quantum oscillations is commonly used to experimentally diagnose topologically non-trivial Fermi surfaces. This methodology, however, is inconclusive for spin-orbit-coupled metals where $pi$-phase-shifts can also arise from non-topological origins. Here, we show that the linear dispersion in topological metals leads to a $T^2$-temperature correction to the oscillation frequency that is absent for parabolic dispersions. We confirm this effect experimentally in the Dirac semi-metal Cd$_3$As$_2$ and the multiband Dirac metal LaRhIn$_5$. Both materials match a tuning-parameter-free theoretical prediction, emphasizing their unified origin. For topologically trivial Bi$_2$O$_2$Se, no frequency shift associated to linear bands is observed as expected. However, the $pi$-phase shift in Bi$_2$O$_2$Se would lead to a false positive in a Landau-fan plot analysis. Our frequency-focused methodology does not require any input from ab-initio calculations, and hence is promising for identifying correlated topological materials.
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The surfaces generated by cleaving non-polar, two-dimensional oxides are often considered to be perfect or ideal. However, single particle spectroscopies on Sr2RuO4, an archetypal non-polar two dimensional oxide, show significant cleavage temperature dependence. We demonstrate that this is not a consequence of the intrinsic characteristics of the surface: lattice parameters and symmetries, step heights, atom positions, or density of states. Instead, we find a marked increase in the density of defects at the mesoscopic scale with increased cleave temperature. The potential generality of these defects to oxide surfaces may have broad consequences to interfacial control and the interpretation of surface sensitive measurements.
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Nanoparticles (size 20, 40 and 60 nm) of Pr_0.5Sr_0.5MnO_3 are prepared by sol-gel technique and their magnetic properties are studied using ferromagnetic resonance and magnetization measurements. A comparison with the properties of the bulk material shows that the ferromagnetic transition at 265 K remains unaffected but the anti-ferromagnetic transition at T_N = 150 K disappears in the nanoparticles. Further, the temperature dependence of magnetic anisotropy shows a complex behavior, being higher in the nanoparticles at high temperatures and lower at lower temperatures in comparison with the bulk.
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