Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userPressure dependence of the exchange interaction in the dimeric single-molecule magnet [Mn4O3Cl4(O2CEt)3(py)3]2 from inelastic neutron scattering
72
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
The low-lying magnetic excitations in the dimer of single-molecule magnets (Mn4)2 are studied by inelastic neutron scattering as a function of hydrostatic pressure. The anisotropy parameters D and B04, which describe each Mn4 subunit, are essentially pressure independent, while the antiferromagnetic exchange coupling J between the two Mn4 subunits strongly depends on pressure, with an increase of 42% at 17 kbar. Additional pressure dependent powder X-ray measurements allow a structural interpretation of the findings.
rate research
Read More
The Q dependence of the inelastic neutron scattering (INS) intensity of transitions within the ground-state spin multiplet of single-molecule magnets (SMMs) is considered. For these transitions, the Q dependence is related to the spin density map in the ground state, which in turn is governed by the Heisenberg exchange interactions in the cluster. This provides the possibility to infer the exchange-coupling constants from the Q dependence of the INS transitions within the spin ground state. The potential of this strategy is explored for the M = +-10 -> +- 9 transition within the S = 10 multiplet of the molecule Mn12 as an example. The Q dependence is calculated for powder as well as single-crystal Mn12 samples for various exchange-coupling situations discussed in the literature. The results are compared to literature data on a powder sample of Mn12 and to measurements on an oriented array of about 500 single-crystals of Mn12. The calculated Q dependence exhibits significant variation with the exchange-coupling constants, in particular for a single-crystal sample, but the experimental findings did not permit an unambiguous determination. However, although challenging, suitable experiments are within the reach of todays instruments.
We performed inelastic neutron scattering measurements on single crystals of NdFe$_{3}$($^{11}$BO$_{3}$)$_{4}$ to explore the magnetic excitations, to establish the underlying Hamiltonian, and to reveal the detailed nature of hybridization between the 4$f$ and 3$d$ magnetism. The observed spectra exhibiting a couple of key features, i.e., anti-crossing of Nd- and Fe-excitations and anisotropy gap at the antiferromagnetic zone center, are explained by the magnetic model including spin interaction in the framework of weakly-coupled Fe$^{3+}$ chains, interaction between the Fe$^{3+}$ and Nd$^{3+}$ moments, and single-ion anisotropy derived from Nd$^{3+}$ crystal field. The combination of the measurements and calculations reveals that the hybridization between 4$f$ and 3$d$ magnetism propagates the local magnetic anisotropy of the Nd$^{3+}$ ion to the Fe$^{3+}$ network, resulting in the bulk structure of multiferroics.
We have investigated the phonon and the magnetic excitations in LaCoO3 by inelastic neutron scattering measurements. The acoustic phonon dispersions show some characteristic features of the folded Brillouin zone (BZ) for the rhombohedrally distorted perovskite structure containing two chemical formula units of LaCoO3 in the unit cell. We observed two transverse optical (TO) phonon branches along (delta, delta, delta), consistent with previously reported Raman active Eg modes which show remarkable softening associated with the spin-state transition [Ishikawa et al., (Phys. Rev. Lett. 93 (2004) 136401.)]. We found that the softening takes place in the TO mode over the whole BZ. In contrast, the acoustic phonons show no anomalous softening associated with the spin-state transition. The low-energy paramagnetic scattering at 8 K is weak, increasing towards a maximum at E > 15 meV, consistent with excitation of the nonmagnetic low-spin to magnetic intermediate-spin state of Co 3+ ions.
We measured two magnetic modes with finite and discrete energies in an antiferromagnetic ordered phase of a geometrically frustrated magnet MgCr2O4 by single-crystal inelastic neutron scattering, and clarified the spatial spin correlations of the two levels: one is an antiferromagnetic hexamer and the other is an antiferromagnetic heptamer. Since these correlation types are emblematic of quasielastic scattering with geometric frustration, our results indicate instantaneous suppression of lattice distortion in an ordered phase by spin-lattice coupling, probably also supported by orbital and charge. The common features in the two levels, intermolecular independence and discreteness of energy, suggest that the spin molecules are interpreted as quasiparticles (elementary excitations with energy quantum) of highly frustrated spins, in analogy with the Fermi liquid approximation.
Time-resolved inelastic neutron scattering measurements on an array of single-crystals of the single-molecule magnet Mn12ac are presented. The data facilitate a spectroscopic investigation of the slow relaxation of the magnetization in this compound in the time domain.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
