Department of Materials Science and Engineering, Norwegian University of Science and Technology, N-7491, Trondheim, Norway.
Dalton Trans. 2011 Aug 7;40(29):7583-9. doi: 10.1039/c1dt10536a. Epub 2011 Jun 24.
Nanocrystalline YMnO(3) has been prepared by wet chemical synthesis routes to obtain crystallites with sizes from 20 nm to bulk material. The crystal structure of hexagonal YMnO(3) nanocrystallites smaller than 80 nm deviates from bulk material in terms of unit cell distortion and unit cell volume. The ferrielectric displacements of Y(3+) cations along the polar c-axis decays progressively with decreasing size below 100 nm. Indications of weak ferromagnetism in the form of a narrow hysteresis loop and enhanced magnetic susceptibility below 43 K in 20 nm YMnO(3) nanoparticles is attributed to extrinsic effects. Low-temperature annealing of the 20 nm crystallites in an oxidizing atmosphere removed all traces of ferromagnetism, showing that this is not a size-induced property. Finally, formation of the competing metastable orthorhombic phase and the thermodynamically stable hexagonal phase is discussed with respect to oxidizing or reducing conditions during synthesis.
通过湿化学合成路线制备了纳米晶 YMnO(3),以获得尺寸从 20nm 到块状材料的晶态。小于 80nm 的六方 YMnO(3)纳米晶的晶体结构在晶胞畸变和晶胞体积方面与块状材料不同。Y(3+)阳离子沿极轴的铁电位移随着尺寸的减小而逐渐衰减,在 100nm 以下。在 20nmYMnO(3)纳米颗粒中,以窄磁滞回线和 43K 以下增强的磁化率形式出现的弱铁磁性归因于外在效应。在氧化气氛下对 20nm 晶粒进行低温退火可以去除所有铁磁性痕迹,表明这不是尺寸诱导的特性。最后,讨论了在合成过程中氧化或还原条件下形成竞争的亚稳正交相和热力学稳定的六方相的情况。