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Register a new userStanding Spin Waves in an Antiferromagnetic Molecular Cr6 Horseshoe
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The antiferromagnetic molecular finite chain Cr6 was studied by inelastic neutron scattering. The observed magnetic excitations at 2.6 and 4.3 meV correspond, due to the open boundaries of a finite chain, to standing spin waves. The determined energy spectrum revealed an essentially classical spin structure. Hence, various spin-wave theories were investigated in order to assess their potential for describing the elementary excitations of finite spin systems.
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The spin-selective electron reflection at a ferromagnetic-paramagnetic interface is investigated using Fe films on a W(110) substrate. Angle-resolved photoemission of the majority and minority Fermi surfaces of the Fe film is used to probe standing wave formation. Intense quantum well states resulting from interfacial reflection are observed exclusively for majority states. Such high spin polarization is explained by the Fermi surface topology of the connecting substrate, and we argue that Fe/W is a particularly suitable interface for that purpose.
High-frequency electron paramagnetic resonance (EPR) studies of the antiferromagnetic Mn-$[3times 3]$ molecular grid clearly reveal a breaking of the $Delta S = 0$ selection rule, providing direct evidence for the mixing of spin wavefunctions ($S$-mixing) induced by the comparable exchange and magneto-anisotropy energy scales within the grid. This finding highlights the potential utility of EPR for studies of exchange splittings in molecular nanomagnets, which is normally considered the sole domain of inelastic neutron scattering, thereby offering improved sensitivity and energy resolution.
We observe coherent spin oscillations in an antiferromagnetic spin-1 Bose-Einstein condensate of sodium. The variation of the spin oscillations with magnetic field shows a clear signature of nonlinearity, in agreement with theory, which also predicts anharmonic oscillations near a critical magnetic field. Measurements of the magnetic phase diagram agree with predictions made in the approximation of a single spatial mode. The oscillation period yields the best measurement to date of the sodium spin-dependent interaction coefficient, determining that the difference between the sodium spin-dependent s-wave scattering lengths $a_{f=2}-a_{f=0}$ is $2.47pm0.27$ Bohr radii.
We report on inelastic neutron scattering (INS) measurements on the molecular spin ring CsFe$_8$, in which eight spin-5/2 Fe(III) ions are coupled by nearest-neighbor antiferromagnetic Heisenberg interaction. We have recorded INS data on a non-deuterated powder sample up to high energies at the time-of-flight spectrometers FOCUS at PSI and MARI at ISIS, which clearly show the excitation of spin waves in the ring. Due to the small number of spin sites, the spin-wave dispersion relation is not continuous but quantized. Furthermore, the system exhibits a gap between the ground state and the first excited state. We have modeled our data using exact diagonalization of a Heisenberg-exchange Hamiltonian together with a small single-ion anisotropy term. Due to the molecules symmetry, only two parameters $J$ and $D$ are needed to obtain excellent agreement with the data. The results can be well described within the framework of the rotational-band model as well as antiferromagnetic spin-wave theories.
The magnetic torque of the antiferromagnetic molecular wheel CsFe8 was studied down to 50 mK and in fields up to 28 T. Below ca. 0.5 K phase transitions were observed at the field-induced level-crossings (LCs). Intermolecular magnetic interactions are very weak excluding an explanation in terms of field-induced magnetic ordering. A magneto-elastic coupling was considered. A generic model shows that the wheel structure is unconditionally unstable at the LCs, and the predicted torque curves explain the essential features of the data well.
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