Tejada et al. Reply

A Reply to the Comment by Lin He

Evidence for Quantization of Mechanical Rotation of Magnetic Nanoparticles

We report evidence of the quantization of the rotational motion of solid particles containing thousands of atoms. A system of CoFe 2 O 4 nanoparticles confined inside polymeric cavities has been studied. The particles have been characterized by the x-ray diffraction, transmission electron microscopy, plasma mass spectroscopy, ferromagnetic resonance (FMR), and magnetization measurements. Magnetic and FMR data confirm the presence of particles that are free to rotate inside the cavities. Equidistant, temperature-independent jumps in the dependence of the microwave absorption on the magnetic field have been detected. This observation is in accordance with the expectation that orbital motion splits the low-field absorption line into multiple lines

High-temperature weak ferromagnetism in a low-density free-electron gas

The magnetic properties of the ground state of a low-density free- electron gas in three dimensions have been the subject of theoretical speculation and controversy for seven decades. Not only is this a difficult theoretical problem to solve, it is also a problem which has not hitherto been directly addressed experimentally. Here we report measurements on electron-doped calcium hexaboride (CaB6) which, we argue, show that - at a density of 7 x 1019 electrons cm-3 - the ground state is ferromagnetically polarized with a saturation moment of 0.07 μ(B) per electron. Surprisingly, the magnetic ordering temperature of this itinerant ferromagnet is 600 K, of the order of the Fermi temperature of the electron gas

Millikelvin magnetic relaxation measurements of alpha-Fe2O3 antiferromagnetic particles

In this paper we report magnetic relaxation data for antiferromagnetic alpha-Fe2O3 particles of 5 nm mean diameter in the temperature range 0.1 K to 25 K. The average spin value of these particles S=124 and the uniaxial anisotropy constant D=1.6x10^-2 K have been estimated from the experimental values of the blocking temperature and anisotropy field. The observed plateau in the magnetic viscosity from 3 K down to 100 mK agrees with the occurrence of spin tunneling from the ground state Sz = S. However, the scaling M vs Tln(nu t) is broken below 5 K, suggesting the occurrence of tunneling from excited states below this temperature.Comment: 4 pages (two columns), 4 figure

Nanoscale magnetic structure and properties of solution-derived self-assembled La0.7Sr0.3MnO3 islands

The following article appeared in Journal of Applied Physics 111.2 (2012): 024307 and may be found at http://scitation.aip.org/content/aip/journal/jap/111/2/10.1063/1.3677985Strain-induced self-assembled La0.7Sr0.3MnO 3 nanoislands of lateral size 50-150 nm and height 10-40 nm have been grown on yttria-stabilized zirconia (001)-substrates from ultradiluted chemical solutions based on metal propionates. The nanoislands grow highly relaxed withstanding the epitaxial relation (001)LSMO[110]//(001) Ysz[010] and show bulk-like average magnetic properties in terms of Curie temperature and saturation magnetization. The interplay of the magnetocrystalline and shape anisotropy within the nanoisland ensemble results in an in-plane magnetic anisotropy with a magnetocrystalline constant K 1(150K) = -(5±1) kJ/m3 and in-plane easy axis along the [110] -La0.7Sr0.3MnO3 direction as measured, for the first time, through ferromagnetic resonance experiments. Magnetic force microscopy studies reveal the correlation between nanoisland size and its magnetic domain structure in agreement with micromagnetic simulations. In particular, we have established the required geometric conditions for single domain, multidomain, and vortex configurations.We acknowledge the financial support from MEC (MAT2008-01022, Consolider NANOSELECT and FPU), Comunidad Autónoma de Madrid (CAM S2009/MAT-1467), Generalitat de Catalunya (Catalan Pla de Recerca 2009-SGR- 770 and XaRMAE), and EU (NESPA). R. D. Zysler and C. A. Ramos acknowledge support from PIP-1333(2007) CONICET and PICT 829 (2006) and PICT 832(2006) ANPCyT of Argentina. Serveis Científic-Tècnics from Universitat de Barcelona and Servei de Micròscopia from Universitat Auto`noma de Barcelona are acknowledged for TEM facilities

Resolving material-specific structures within Fe₃O₄|γ-Mn₂O₃ core|shell nanoparticles using anomalous small-angle X-ray scattering

Here it is demonstrated that multiple-energy, anomalous small-angle X-ray scattering (ASAXS) provides significant enhancement in sensitivity to internal material boundaries of layered nanoparticles compared with the traditional modeling of a single scattering energy, even for cases in which high scattering contrast naturally exists. Specifically, the material-specific structure of monodispersed Fe₃O₄|γ-Mn₂O₃ core|shell nanoparticles is determined, and the contribution of each component to the total scattering profile is identified with unprecedented clarity. We show that Fe₃O₄|γ-Mn₂O₃ core|shell nanoparticles with a diameter of 8.2 ± 0.2 nm consist of a core with a composition near Fe₃O₄ surrounded by a (Mn(x)Fe(1-x))₃O₄ shell with a graded composition, ranging from x ≈ 0.40 at the inner shell toward x ≈ 0.46 at the surface. Evaluation of the scattering contribution arising from the interference between material-specific layers additionally reveals the presence of Fe₃O₄ cores without a coating shell. Finally, it is found that the material-specific scattering profile shapes and chemical compositions extracted by this method are independent of the original input chemical compositions used in the analysis, revealing multiple-energy ASAXS as a powerful tool for determining internal nanostructured morphology even if the exact composition of the individual layers is not known a priori

Size-Dependent passivation shell and magnetic properties in antiferromagnetic/ferrimagnetic core/shell MnO nanoparticles

The magnetic properties of bimagnetic core/shell nanoparticles consisting of an antiferromagnetic MnO core and a ferrimagnetic passivation shell have been investigated. It is found that the phase of the passivation shell (γ-Mn2O3 or Mn3O4) depends on the size of the nanoparticles. Structural and magnetic characterizations concur that while the smallest nanoparticles have a predominantly γ-Mn2O3 shell, larger ones have increasing amounts of Mn3O4. A considerable enhancement of the Néel temperature, TN, and the magnetic anisotropy of the MnO core for decreasing core sizes has been observed. The size reduction also leads to other phenomena such as persistent magnetic moment in MnO up to high temperatures and an unusual temperature behavior of the magnetic domains