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La0.5Ca0.5MnO3纳米颗粒中电荷和反铁磁有序的抑制

Suppression of charge and antiferromagnetic ordering in La0.5Ca0.5MnO3 nanoparticles.

作者信息

Giri Samir Kumar, Nath Tapan Kumar

机构信息

Department of Physics and Meteorology, Indian Institute of Technology, Kharagpur, West Bengal 721302, India.

出版信息

J Nanosci Nanotechnol. 2011 Jun;11(6):4806-14. doi: 10.1166/jnn.2011.4139.

Abstract

The intermediate band-width manganite La0.5Ca0.5MnO3 has a CE type charge, orbital and antiferromagnetic order below 195 K owing to strong electronic correlation and commensurability effect. We have critically investigated in details all the possible mechanisms behind the destabilization of charge/orbital ordering in La0.5Ca0.5MnO3 with the reduction of grain size in the nanometric regime as evidenced from our various experimental results. We have tried to found out a universal scenario to explain such behavior in nanometric manganites in general. This study shows that the room temperature Pnma perovskite structure, correlated with the lattice distortion, Mn-O distances and octahedral tilts, is practically unaffected with the reduction of particle size. However, in these nanocrystalline La0.5Ca0.5MnO3, the stable charge ordered state with antiferromagnetic ordering becomes significantly suppressed and FM ordering spontaneously appears below T(c) = 260 K as compared to its bulk counterpart. From strong experimental evidences on nano and bulk manganites, we revisit this issue and also discuss the absence of correlation between size reduction and pressure effects on manganites. We argue from a phenomenological analysis that the above observations could be best attributed to enhanced surface disorder in the nanosized half-doped manganite grains which is likely to be general in all nano size charge ordered manganites.

摘要

中间带宽的锰氧化物La0.5Ca0.5MnO3由于强电子关联和可公度效应,在195K以下具有CE型电荷、轨道和反铁磁序。我们已经详细且批判性地研究了La0.5Ca0.5MnO3中电荷/轨道序失稳背后所有可能的机制,这种失稳是由纳米尺度下晶粒尺寸的减小导致的,我们的各种实验结果证明了这一点。我们试图找出一个通用的情形来解释一般纳米锰氧化物中的这种行为。这项研究表明,与晶格畸变、Mn - O距离和八面体倾斜相关的室温Pnma钙钛矿结构实际上不受粒径减小的影响。然而,在这些纳米晶La0.5Ca0.5MnO3中,具有反铁磁序的稳定电荷有序态被显著抑制,并且与块体材料相比,在T(c)=260K以下自发出现铁磁序。基于对纳米和块体锰氧化物的有力实验证据,我们重新审视了这个问题,并讨论了粒径减小与锰氧化物压力效应之间缺乏相关性的情况。我们从现象学分析中认为,上述观察结果最有可能归因于纳米尺寸的半掺杂锰氧化物晶粒中表面无序的增强,这在所有纳米尺寸的电荷有序锰氧化物中可能是普遍存在的。

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