Strain relaxation mechanisms of elastic softening and twin wall freezing associated with structural phase transitions in (Ca,Sr)TiO3 perovskites.

Resonant ultrasound spectroscopy has been used to measure the bulk modulus (K), shearmodulus (G) and acoustic dissipation of polycrystalline perovskite samples across theCaTiO(3)­SrTiO(3) solid solution in the temperature range ∼10­1350 K. A remarkable pattern of up to ∼25% softening of G as a function of both temperature and composition is due to coupling of shear strain with order parameters for the Pm3m ↔ I 4/mcm, I 4/mcm↔Pnmaand I 4/mcm↔Pbcm transitions. Anomalies in K associated with the phase transitions are small, consistent with only weak coupling of octahedral tilting order parameter(s) with volume strain. A change from tricritical character for the Pm3m ↔ I 4/mcm transition towards second order character at Sr-rich compositions appears to be due to changing properties of the soft optic mode rather than to changes in magnitude of strain/order parameter coupling coefficients. Precursor softening of G ahead of the Pm3m ↔ I 4/mcm transition, due tof luctuations or clustering, occurs over a temperature interval of up to ∼200 K, and also changes character at the most Sr-rich compositions. The tetragonal structure with Sr-rich compositions is characterized by additional softening with falling temperature which is most likely related to the proximity of a ferroelectric instability. The I 4/mcm↔Pnma transition is accompanied by stiffening, which is attributed to the effects of strong coupling between order parameters for M-point and R-point tilting. The pattern of attenuation at RUS frequencies in the tetragonal phase can be understood in terms of the mobility of twin walls which be come pinned below ∼500 K, and the loss mechanism most likely involves local bowing of the walls by lateral motion of ledges rather than the advance and retraction of needle tips. Twin wall mobility is suppressed in the orthorhombic structure.

Magneto-orbital helices as a route to coupling magnetism and ferroelectricity in multiferroic CaMn7O12.

Orbital physics drives a rich phenomenology in transition-metal oxides, providing the microscopic underpinning for effects such as Colossal Magnetoresistance. In particular, magnetic and lattice degrees of freedom are coupled through orbital ordering, and it has long been hoped that this coupling could be exploited to create high-temperature multiferroics with large values of the electrical polarization. Here we report an unprecedented magneto-orbital texture in multiferroic CaMn(7)O(12), found to give rise to the largest magnetically induced ferroelectric polarization measured to date. X-ray diffraction characterization of the structural modulation in these 'magneto-orbital helices', and analysis of magnetic exchange shows that orbital order is crucial in stabilising a chiral magnetic structure, thus allowing for electric polarization. Additionally, the presence of a global structural rotation enables the coupling between this polarization and magnetic helicity required for multiferroicity. These novel principles open up the possibility of discovering new multiferroics with even larger polarization and higher transition temperatures.