Multi-Technique Experimental Benchmarking of the Local Magnetic Anisotropy of a Cobalt(II) Single-Ion Magnet.

A comprehensive understanding of the ligand field and its influence on the degeneracy and population of d-orbitals in a specific coordination environment are crucial for the rational design and enhancement of magnetic anisotropy of single-ion magnets (SIMs). Herein, we report the synthesis and comprehensive magnetic characterization of a highly anisotropic CoII SIM, [L2Co](TBA)2 (L is an N,N'-chelating oxanilido ligand), that is stable under ambient conditions. Dynamic magnetization measurements show that this SIM exhibits a large energy barrier to spin reversal U eff > 300 K and magnetic blocking up to 3.5 K, and the property is retained in a frozen solution. Low-temperature single-crystal synchrotron X-ray diffraction used to determine the experimental electron density gave access to Co d-orbital populations and a derived U eff, 261 cm-1, when the coupling between the d x 2 - y 2 and dxy orbitals is taken into account, in very good agreement with ab initio calculations and superconducting quantum interference device results. Powder and single-crystal polarized neutron diffraction (PNPD, PND) have been used to quantify the magnetic anisotropy via the atomic susceptibility tensor, revealing that the easy axis of magnetization is pointing along the N-Co-N' bisectors of the N,N'-chelating ligands (3.4° offset), close to the molecular axis, in good agreement with complete active space self-consistent field/N-electron valence perturbation theory to second order ab initio calculations. This study provides benchmarking for two methods, PNPD and single-crystal PND, on the same 3d SIM, and key benchmarking for current theoretical methods to determine local magnetic anisotropy parameters.

Field-tunable toroidal moment in a chiral-lattice magnet.

Ferrotoroidal order, which represents a spontaneous arrangement of toroidal moments, has recently been found in a few linear magnetoelectric materials. However, tuning toroidal moments in these materials is challenging. Here, we report switching between ferritoroidal and ferrotoroidal phases by a small magnetic field, in a chiral triangular-lattice magnet BaCoSiO4 with tri-spin vortices. Upon applying a magnetic field, we observe multi-stair metamagnetic transitions, characterized by equidistant steps in the net magnetic and toroidal moments. This highly unusual ferri-ferroic order appears to come as a result of an unusual hierarchy of frustrated isotropic exchange couplings revealed by first principle calculations, and the antisymmetric exchange interactions driven by the structural chirality. In contrast to the previously known toroidal materials identified via a linear magnetoelectric effect, BaCoSiO4 is a qualitatively new multiferroic with an unusual coupling between several different orders, and opens up new avenues for realizing easily tunable toroidal orders.

Ferromagnetic Cr4PtGa17: A Half-Heusler-Type Compound with a Breathing Pyrochlore Lattice.

We describe the crystal structure and elementary magnetic properties of a previously unreported ternary intermetallic compound, Cr4PtGa17, which crystallizes in a rhombohedral unit cell in the noncentrosymmetric space group R3m. The crystal structure is closely related to those of XYZ half-Heusler compounds, where X, Y, and Z are reported to be single elements only, occupying three different face-centered-cubic sublattices. The new material, Cr4PtGa17, can be most straightforwardly illustrated by writing the formula as (PtGa2)(Cr4Ga14)Ga (X = PtGa2, Y = Cr4Ga14, Z = Ga); that is, the X and Y sites are occupied by clusters instead of single elements. The magnetic Cr occupies a breathing pyrochlore lattice. Ferromagnetic ordering is found below TC ∼ 61 K, by both neutron diffraction and magnetometer studies, with a small, saturated moment of ∼0.25 µB/Cr observed at 2 K, making Cr4PtGa17 the first ferromagnetically ordered material with a breathing pyrochlore lattice. A magnetoresistance of ∼140% was observed at 2 K. DFT calculations suggest that the material has a nearly half-metallic electronic structure. The new material, Cr4PtGa17, the first realization of both a half-Heusler-type structure and a breathing pyrochlore lattice, might pave a new way to achieve novel types of half-Heusler compounds.

Efficient Low-Grade Heat Harvesting Enabled by Tuning the Hydration Entropy in an Electrochemical System.

Harvesting of low-grade heat (<100 °C) is promising, but its application is hampered by a lack of efficient and low-cost systems. The thermally regenerative electrochemical cycle (TREC) is a potential alternative system with high energy-conversion efficiency. Here, the temperature coefficient (α), which is a key factor in a TREC, is studied by tuning the hydration entropy of the electrochemical reaction. The change of α in copper hexacyanoferrate (CuHCFe) with intercalation of different monovalent cations (Na+ , K+ , Rb+ , and Cs+ ) and a larger α value of -1.004 mV K-1 being found in the Rb+ system are observed. With a view to practical application, a full cell is constructed for low-grade heat harvesting. The resultant ηe is 4.34% when TREC operates between 10 and 50 °C, which further reaches 6.21% when 50% heat recuperation is considered. This efficiency equals to 50% of the Carnot efficiency, which is thought to be the highest ηe reported for low-grade heat harvesting systems. This study provides a fundamental understanding of the mechanisms governing the TREC, and the demonstrated efficient system paves the way for low-grade heat harvesting.

Field-induced self-assembly of iron oxide nanoparticles investigated using small-angle neutron scattering.

The magnetic-field-induced assembly of magnetic nanoparticles (NPs) provides a unique and flexible strategy in the design and fabrication of functional nanostructures and devices. We have investigated the field-induced self-assembly of core-shell iron oxide NPs dispersed in toluene by means of small-angle neutron scattering (SANS). The form factor of the core-shell NPs was characterized and analyzed using SANS with polarized neutrons. Large-scale aggregates of iron oxide NPs formed above 0.02 T as indicated by very-small-angle neutron scattering measurements. A three-dimensional long-range ordered superlattice of iron oxide NPs was revealed under the application of a moderate magnetic field. The crystal structure of the superlattice has been identified to be face-centred cubic.

Electrodeposition of FeCoCd films with in-plane uniaxial magnetic anisotropy for microwave applications.

FeCoCd thin films with 500 nm thickness are directly prepared through electrodeposition in the sulphate bath in which glycine and citric acid were added as complex agents. The composition, structure, and magnetic of FeCoCd films were investigated as a function of Cd2+ concentration, cathode current density, and deposition temperature. A wonderful soft magnetic FeCoCd film was prepared and its coercivity of easy axis and hard axis are 5 Oe and 4 Oe, respectively. The natural resonance frequency is about 3.0 GHz, which imply that the FeCoCd film is potential candidate for high frequency applications.