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J. P. Embs

Publications and source records attributed to J. P. Embs.

7 recordsLinked to original sources

Exotic magnetism and persistent short-range spin correlations in a frustrated honeycomb lattice antiferromagnet

Two-dimensional high-spin bipartite honeycomb networks, where anisotropy, competing exchange interactions, and spin fluctuations interplay, provide an alternative platform to test theoretical models that distinguish between classical and quantum magnetism in the context of emergent many-body phenomena and exotic excitations. Here, we report the crystal structure, magnetization, specific heat, and inelastic neutron scattering measurements of the $S = 5/2$ distorted honeycomb magnet $\mathrm{CaZn_2Fe(PO_4)_3}$. Magnetization measurements reveal dominant antiferromagnetic interactions between the $\mathrm{Fe^{3+}}$ ($S = 5/2$) moments. The development and field evolution of a dip in the magnetic susceptibility under an external magnetic field indicate an unconventional field-induced transition, further supported by anomalies observed in magnetization isotherms. Zero-field specific heat measurements show an antiferromagnetic transition at $T_N \approx 1.67 \mathrm{K}$, which evolves under applied magnetic field, suggesting stabilization of a field-induced spin-canted state. Thermodynamic measurements reveal short-range spin correlations above the transition temperature. Inelastic neutron scattering results further corroborate antiferromagnetic ordering, consistent with specific heat data. Spin-wave calculations indicate competing exchange interactions that introduce magnetic frustration, along with weak Ising-like anisotropy. The interplay of competing interactions and anisotropy gives rise to exotic field-induced behavior and places the system in close proximity to a mean-field tricritical point in the $J_2/J_1$--$J_3/J_1$ phase diagram, opening a route to unconventional states in high-spin frustrated honeycomb magnets.

cond-mat.str-el

Magnetic order and exchange couplings in the frustrated diamond lattice antiferromagnet MnSc$_2$Se$_4$

We report the magnetic properties of $A$-site spinel compound MnSc$_2$Se$_4$. The macroscopic magnetic measurements uncovers successive magnetic transitions at $T_{\rm{N1}}$= 2.04 K, followed by two further transitions at $T_{\rm{N2}}$=1.8 K and $T_{\rm{N3}}$=1.6 K. Neutron powder diffraction reveals that both, $T_{\rm{N2}} < T < T_{\rm{N1}}$ and $T <T_{\rm{N3}}$, orders are associated with the propagation vector $k$=(3/4 3/4 0), while the magnetic structures are collinear amplitude modulated and helical, respectively. Using neutron powder spectroscopy we demonstrated the effect of substitution of S by Se on the magnetic exchange. The energy range of the spin-wave excitations is supressed due to the chemical pressure of the $X$- ion in MnSc$_2X_4$ ($X$=S, Se) spinels.

cond-mat.str-el

Propagation of defects in doped magnetic materials of different dimensionality

Defects intentionally introduced into magnetic materials often have a profound effect on the physical properties. Specifically tailored neutron spectroscopic experiments can provide detailed information on both the local exchange interactions and the local distances between the magnetic atoms around the defects. This is demonstrated for manganese dimer excitations observed for the magnetically diluted three- and two-dimensional compounds KMn(x)Zn(1-x)F(3) and K(2)Mn(x)Zn(1-x)F(4), respectively. The resulting local exchange interactions deviate up to 10% from the average, and the local Mn-Mn distances are found to vary stepwise with increasing internal pressure due to the Mn/Zn substitution. Our analysis qualitatively supports the theoretically predicted decay of atomic displacements according to 1/r**2, 1/r, and constant (for three-, two-, and one-dimensional compounds, respectively) where r denotes the distance of the displaced atoms from the defect.

cond-mat.mtrl-sci

Crystal-field interaction and oxygen stoichiometry effects in strontium-doped rare-earth cobaltates

Inelastic neutron scattering was employed to study the crystal-field interaction in the strontium-doped rare-earth compounds R(x)Sr(1-x)CoO(3-z) (R=Pr, Nd, Ho, and Er). Particular emphasis is laid on the effect of oxygen deficiencies which naturally occur in the synthesis of these compounds. The observed energy spectra are found to be the result of a superposition of crystal fields with different nearest-neighbor oxygen coordination at the R sites. The experimental data are interpreted in terms of crystal-field parameters which behave in a consistent manner through the rare-earth series, thereby allowing a reliable extrapolation for rare-earth ions not considered in the present work.

cond-mat.mtrl-sci

Direct observation of local Mn-Mn distances in the paramagnetic compound CsMnxMg1-xBr3

We introduce a novel method for local structure determination with a spatial resolution of the order of 0.01 Angstroem. It can be applied to materials containing clusters of exchange-coupled magnetic atoms. We use neutron spectroscopy to probe the energies of the cluster excitations which are determined by the interatomic coupling strength J. Since for most materials J is related to the interatomic distance R through a linear relation dJ/dR=α (for dR/R<<1), we can directly derive the local distance R from the observed excitation energies. This is exemplified for the mixed one-dimensional paramagnetic compound CsMnxMg1 xBr3 (x=0.05, 0.10) containing manganese dimers oriented along the hexagonal c-axis. Surprisingly, the resulting Mn-Mn distances R do not vary continuously with increasing internal pressure, but lock in at some discrete values.

cond-mat.mtrl-sci

Ferromagnetic and antiferromagnetic dimer splittings in LaMn0.1Ga0.9O3

Inelastic neutron scattering was employed to study the magnetic excitations of Mn3+ dimers in LaMn0.1Ga0.9O3. The nearest-neighbor interaction of Mn3+ ions is ferromagnetic in the basal (a,b)-plane, but antiferromagnetic along the c-direction, thus two different types of dimer excitations are simultaneously present in the experiments. From the observed energy spectra we derive Heisenberg-type exchange interactions Jab=0.210(4) meV and Jc=-0.285(5) meV as well as an axial anisotropy parameter D=0.036(6) meV. These parameters considerably differ from those derived for the isostructural parent compound LaMnO3 due to structural effects.

cond-mat.str-el

Magnetization of rotating ferrofluids: the effect of polydispersity

The influence of polydispersity on the magnetization is analyzed in a nonequilibrium situation where a cylindrical ferrofluid column is enforced to rotate with constant frequency like a rigid body in a homogeneous magnetic field that is applied perpendicular to the cylinder axis. Then, the magnetization and the internal magnetic field are not longer parallel to each other and their directions differ from that of the applied magnetic field. Experimental results on the transverse magnetization component perpendicular to the applied field are compared and analyzed as functions of rotation frequency and field strength with different polydisperse Debye models that take into account the polydispersity in different ways and to a varying degree.

physics.flu-dyn