因此体系自发地相分离为铁磁团簇、非磁基底和自旋玻璃相。
Therefore, it is concluded that the phase-separated state in cobaltites consist of FM clusters and non-FM matrix, and spin glass-like regions.
“研发这类发动机的部分原因是为了避免使用稀土磁材，但主要目的还是为了降低成本，”大陆集团混合动力和电力汽车项目负责人MikeCrane说。
Part of the rationale for developing this motor is to avoid rare earth metals, but it mostly is a move to lower costs, said Mike Crane, who runs Continental's hybrid and electric vehicle programs.
汽车部件生产商德国大陆集团的执行官介绍说：“即便在供应最充足的情况下，稀土磁的价格也是非常昂贵的。”
Even in the best scenario of supply these [rare earth] magnets are very expensive.
结果表明，此样品在居里点附近由铁磁向顺磁过渡，且表现出典型的团簇玻璃特征。
Magnetic properties indicate the transition from ferromagnetic to paramagnetic near the Curie point, and exhibit the typical cluster glass characterization.
为了研究磁光阱冷原子团所在区域的磁场大小，从而得出磁场零点附近磁场的微弱变化及其分布。
In order to make sure the magnetic field distribution around the magneto optical trap cold atoms, the weak variation and distribution around the zero point magnet field can be analyzed.
低温下始终出现自旋玻璃或团簇玻璃行为，说明存在反铁磁与铁磁的相互竞争。
All the compounds are spin-glass or cluster-glass phase below a certain temperature due to the competition between the antiferromagnetic and ferromagnetic correlations.
研究表明，这一奇异的矫顽力特性与液相基底表面铁薄膜中的原子团簇尺寸分布、无序的薄膜表面磁各向异性以及团簇间的磁性相互作用等因素有关。
Our experimental results show that the anomalous magnetic properties are due to the non-uniform particle size distribution, random surface anisotropy and interparticle interactions in the films.
观测表明，多数磁尾等离子体团为具有强核心场的通量绳结构。
It was demonstrated from the observations that most plasmoids in the magnetotail are the flux rope structures with a large core field.
同时，还可以通过选择功能性的中心金属离子和具有功能官能团的有机配体赋予目标金属配位聚合物以光、电、磁等功能。
At the same time, metal coordination polymers can be endowed with optics, electric and magnetism by selecting functional metal ions and organic ligands with functional groups.
同时，还可以通过选择功能性的中心金属离子和具有功能官能团的有机配体赋予目标金属配位聚合物以光、电、磁等功能。
At the same time, metal coordination polymers can be endowed with optics, electric and magnetism by selecting functional metal ions and organic ligands with functional groups.
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