Virginie Simonet

Magnetic-rare-earth pyrochlore iridates exhibit a rich variety of unconventional phases, driven by the complex interactions within and between the rare-earth and the iridium sublattices. In this study, we investigate the peculiar magnetic state of Tb 2 Ir 2 O 7 , where a component of the Tb 3 + moment orders perpendicular to its local Ising anisotropy axis. By means of neutron diffraction and inelastic neutron scattering down to dilution temperatures, complemented by specific heat measurements, we show that this intriguing magnetic state is fully established at 1.5 K and we characterize its excitation spectrum across a broad range of energies. Our calculations reveal that bilinear interactions between Tb 3 + ions subjected to the Ir molecular field capture several key features of the experiments, but need to be supplemented to fully reproduce the observed behavior.

Combining macroscopic measurements, neutron scattering, and modeling, we identify in the GeFe_{2}O_{4} spinel a correlated paramagnetic state resulting from the predominance of third-neighbor antiferromagnetic interactions. These interactions materialize four interlaced families of triangular planes with 120° spins emerging from the underlying pyrochlore lattice. At lower temperatures, a phase transition occurs to a noncoplanar spin structure that is characterized by six propagation vectors. This unusual multi-q order is triggered by the presence of weaker interactions up to the sixth neighbors. The system is remarkably successful in coupling the different triangular planes while maintaining their two-dimensional 120° order. Our Letter highlights the hierarchy of interactions involved in GeFe_{2}O_{4}, which is singular among spinel compounds since first-neighbor interactions are only a small fraction of the dominant third-neighbor ones.

Magnetic-rare-earth pyrochlore iridates exhibit a rich variety of unconventional phases, driven by the complex interactions within and between the rare-earth and the iridium sublattices. In this study, we investigate the peculiar magnetic state of Tb$_{2}$Ir$_{2}$O$_{7}$, where a component of the Tb$^{3+}$ moment orders perpendicular to its local Ising anisotropy axis. By means of neutron diffraction and inelastic neutron scattering down to dilution temperatures, complemented by specific heat measurements, we show that this intriguing magnetic state is fully established at 1.5 K and we characterize its excitation spectrum across a broad range of energies. Our calculations reveal that bilinear interactions between Tb$^{3+}$ ions subjected to the Ir molecular field capture several key features of the experiments, but need to be supplemented to fully reproduce the observed behavior.

Geometrical frustration, as in pyrochlore lattices made of corner-sharing tetrahedra, precludes the onset of conventional magnetic ordering, enabling the stabilization of fluctuating spin states at low temperature. Disorder is a subtle ingredient that can modify the nature of these exotic non-ordered phases. Here, we study the interplay between disorder and magnetic frustration in the new pyrochlore Tb$_{2}$ScNbO$_{7}$ where the non magnetic site presents a charge disorder Nb$^{5+}$/Sc$^{3+}$. Its quantification with sophisticated diffraction techniques (electrons, X-rays, neutrons) allows us to estimate the distribution of the splitting of the magnetic Tb$^{3+}$ non-Kramers ground state doublets and to compare it with excitations measured in inelastic neutron scattering. Combining macroscopic and neutron scattering measurements, we show that a clear spin glass transition at 1 K stems out while retaining strong spin liquid correlations. Our results suggest that Tb$_{2}$ScNbO$_{7}$ stabilizes one of the novel disorder induced quantum spin liquid or topological glassy phases recently proposed theoretically.