论文标题
部分可观测时空混沌系统的无模型预测
Possible helimagnetic order in Co4+-containing perovskites Sr1-xCaxCoO3
论文作者
论文摘要
我们通过高压技术系统地合成了钙钛矿型氧化物SR1-XCAXCOO3,其中含有异常高的价CO4+离子,并研究了系统晶格变化对磁性和电子特性的影响。随着CA含量X超过约0.6,结构从立方体变为正晶,这得到了焓的第一原理计算的支持。在正骨变形时,基态显然是铁磁性的,略微下降了居里温度。重要的是,X大于0.8的化合物在最低温度下表现出抗铁磁行为,其温度为阳性,并在最低温度下进行非线性磁化曲线,这意味着基态是非共线性抗firyeromagnetic或Helimagnetic。考虑到高X区域在高X区域的电子特异性热的抑制,因此,通过频带宽度缩小以及具有负电荷转移能量的双交换机制,以及由于下一个nearest邻居的启动,讨论了SR1-XCAXCOO3中helimagnetic态的可能出现。
We systematically synthesized perovskite-type oxides Sr1-xCaxCoO3 containing unusually high valence Co4+ ions by a high pressure technique, and investigated the effect of systematic lattice change on the magnetic and electronic properties. As the Ca content x exceeds about 0.6, the structure changes from cubic to orthorhombic, which is supported by the first-principles calculations of enthalpy. Upon the orthorhombic distortion, the ground state remains to be apparently ferromagnetic with a slight drop of the Curie temperature. Importantly, the compounds with x larger than 0.8 show antiferromagnetic behavior with positive Weiss temperatures and nonlinear magnetization curves at lowest temperature, implying that the ground state is noncollinear antiferromagnetic or helimagnetic. Considering the incoherent metallic behavior and the suppression of the electronic specific heat at high x region, the possible emergence of a helimagnetic state in Sr1-xCaxCoO3 is discussed in terms of the band-width narrowing and the double-exchange mechanism with the negative charge transfer energy as well as the spin frustration owing to the next-nearest neighbor interaction.