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A-site disorder effects in electron-doped manganite La0.4Ca0.6MnO3

机译:电子掺杂锰La 0.4 Ca 0.6 MnO 3 的A位无序效应

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The A-site disorder effects on the stability of charge-ordered state in electron-doped manganite R0.4A0.6MnO3 (where R = La, Pr, Nd, Sm, and A = Ca, Sr, Ba) are investigated by detailed measurements of transport, magnetism, and specific heat. The robust charge-ordered phase within the prototype sample can be successively suppressed by enhancing the A-site disorder, and finally an atomic-scale spin-glass state is evidenced in the highest disordered sample. However, no ferromagnetic phase can be observed; even the long-range charge-ordered antiferromagnetic phase is fully suppressed, which can be associated with the insufficient e g electron density in such an electron-doped manganite. This revealing is helpful for understanding the origin of ferromagnetic phase in nano-sized or B-site doped charge-ordered manganites with small e g electron density.
机译:A位无序对掺杂电子的锰矿R 0.4 A 0.6 MnO 3 中电荷有序态稳定性的影响(其中R = La,Pr,Nd,Sm和A = Ca,Sr,Ba)是通过对传输,磁性和比热的详细测量来研究的。可以通过增强A-位无序性来连续抑制原型样品中的强电荷有序相,最后在最高无序样品中证明了原子级自旋玻璃态。但是,没有观察到铁磁相。即使是长程有序的反铁磁相也被完全抑制,这可能与这种掺杂电子的锰矿中e g 电子密度不足有关。这一发现有助于理解电子密度低的 g 纳米或B-位掺杂的电荷有序锰矿中铁磁相的起源。

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