论文标题
通过化学压力和单轴应变调整A2CR3AS3三元砷中的A2CR3AS3三元砷中的链互磁不稳定性
Tuning interchain ferromagnetic instability in A2Cr3As3 ternary arsenides by chemical pressure and uniaxial strain
论文作者
论文摘要
我们分析了碱金属取代和单轴应变对A2CR3AS3(a = Na,k,rb,cs)中磁性磁性诱导的化学压力的影响,具有准尺寸结构。在密度功能理论的框架内,我们预测,非磁性相非常接近3D共线铁磁性状态,该状态在中等相关性的状态下意识到,由于不同的不同链链铁电磁耦合,因此家庭中所有成员的这种趋势都很小。我们发现,这种链铁磁耦合的稳定性具有非单调的行为,并增加了阳离子的大小,与沿链方向的CR-AS-AS-CR键合的结构扭曲程度密切相关。特别是,我们证明在RB的情况下,它与最近的实验一致。我们还表明,单轴菌株是一种可行的工具,可以将非磁相调整到链铁磁不稳定性方向。晶胞内Cr三角形的形状的修饰有利于链中链中的净磁化形成,并在链中的铁磁耦合形成。这项研究可以提供有关此类材料中超导性和磁性之间相互作用的相关见解。
We analyze the effects of chemical pressure induced by alkali metal substitution and uniaxial strain on magnetism in the A2Cr3As3 (A = Na, K, Rb, Cs) family of ternary arsenides with quasi-one dimensional structure. Within the framework of the density functional theory, we predict that the non-magnetic phase is very close to a 3D collinear ferrimagnetic state, which realizes in the regime of moderate correlations, such tendency being common to all the members of the family with very small variations due to the different interchain ferromagnetic coupling. We uncover that the stability of such interchain ferromagnetic coupling has a non-monotonic behavior with increasing the cation size, being critically related to the degree of structural distortions which is parametrized by the Cr-As-Cr bonding angles along the chain direction. In particular, we demonstrate that it is boosted in the case of the Rb, in agreement with recent experiments. We also show that uniaxial strain is a viable tool to tune the non-magnetic phase towards an interchain ferromagnetic instability. The modifcation of the shape of the Cr triangles within the unit cell favors the formation of a net magnetization within the chain and of a ferromagnetic coupling among the chains. This study can provide relevant insights about the interplay between superconductivity and magnetism in this class of materials.