Room-temperature polar ferromagnet ScFeO3 transformed from a high-pressure orthorhombic perovskite phase.

Multiferroic materials have been the subject of intense study, but it remains a great challenge to synthesize those presenting both magnetic and ferroelectric polarizations at room temperature. In this work, we have successfully obtained LiNbO3-type ScFeO3, a metastable phase converted from the orthorhombic perovskite formed under 15 GPa at elevated temperatures. A combined structure analysis by synchrotron X-ray and neutron powder diffraction and high-angle annular dark-field scanning transmission electron microscopy imaging reveals that this compound adopts the polar R3c symmetry with a fully ordered arrangement of trivalent Sc and Fe ions, forming highly distorted ScO6 and FeO6 octahedra. The calculated spontaneous polarization along the hexagonal c-axis is as large as 100 µC/cm(2). The magnetic studies show that LiNbO3-type ScFeO3 is a weak ferromagnet with TN = 545 K due to a canted G-type antiferromagnetic ordering of Fe(3+) spins, representing the first example of LiNbO3-type oxides with magnetic ordering far above room temperature. A comparison of the present compound and rare-earth orthorhombic perovskites RFeO3 (R = La-Lu and Y), all of which possess the corner-shared FeO6 octahedral network, allows us to find a correlation between TN and the Fe-O-Fe bond angle, indicating that the A-site cation-size-dependent octahedral tilting dominates the magnetic transition through the Fe-O-Fe superexchange interaction. This work provides a general and versatile strategy to create materials in which ferroelectricity and ferromagnetism coexist at high temperatures.

Plasmonically controlled lasing resonance with metallic-dielectric core-shell nanoparticles.

We experimentally demonstrate the capability of tailoring lasing resonance properties by manipulating the coupling between surface plasmons and photons in random lasing media composed of metallic-dielectric core-shell nanoparticles and organic dyes. It is revealed that core-shell nanoparticle-based systems exhibit optical feedback features distinctive from those containing pure metallic nanoparticles, provided that the scattering strength is weak enough. The pump threshold increases with an increment in the shell thickness, which can provide a direct proof that the local field enhancement plays a central role in the emergence of coherent feedback. The anomalous behavior in both threshold and optical feedback is discussed in terms of the modification of fluorescent properties of fluorophores close to metallic surface.