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三角反铁磁体中由挫折诱导的纳米尺度不均匀性。

Frustration-induced nanometre-scale inhomogeneity in a triangular antiferromagnet.

作者信息

Zorko A, Adamopoulos O, Komelj M, Arčon D, Lappas A

机构信息

1] Jožef Stefan Institute, Jamova c. 39, 1000 Ljubljana, Slovenia [2] EN-FIST Centre of Excellence, Dunajska c. 156, SI-1000 Ljubljana, Slovenia.

Institute of Electronic Structure and Laser, Foundation for Research and Technology-Hellas, Vassilika Vouton, 71110 Heraklion, Greece.

出版信息

Nat Commun. 2014;5:3222. doi: 10.1038/ncomms4222.

Abstract

Phase inhomogeneity of otherwise chemically homogenous electronic systems is an essential ingredient leading to fascinating functional properties, such as high-Tc superconductivity in cuprates, colossal magnetoresistance in manganites and giant electrostriction in relaxors. In these materials distinct phases compete and can coexist owing to intertwined ordered parameters. Charge degrees of freedom play a fundamental role, although phase-separated ground states have been envisioned theoretically also for pure spin systems with geometrical frustration that serves as a source of phase competition. Here we report a paradigmatic magnetostructurally inhomogenous ground state of the geometrically frustrated α-NaMnO2 that stems from the system's aspiration to remove magnetic degeneracy and is possible only due to the existence of near-degenerate crystal structures. Synchrotron X-ray diffraction, nuclear magnetic resonance and muon spin relaxation show that the spin configuration of a monoclinic phase is disrupted by magnetically short-range-ordered nanoscale triclinic regions, thus revealing a novel complex state of matter.

摘要

在化学性质均匀的电子系统中,相的不均匀性是导致出现迷人功能特性的一个关键因素,例如铜酸盐中的高温超导性、锰酸盐中的巨磁电阻以及弛豫铁电体中的巨大电致伸缩效应。在这些材料中,不同的相相互竞争,由于有序参数相互交织而能够共存。电荷自由度起着根本性作用,尽管理论上也设想过对于具有几何阻挫的纯自旋系统存在相分离基态,而几何阻挫是相竞争的一个来源。在此,我们报道了几何阻挫的α-NaMnO₂的一种典型磁结构不均匀基态,它源于该系统消除磁简并的倾向,并且仅由于存在近简并晶体结构才有可能出现。同步辐射X射线衍射、核磁共振和μ子自旋弛豫表明,单斜相的自旋构型被磁短程有序的纳米级三斜区域破坏,从而揭示了一种新型的复杂物质状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc39/4273263/5fa714775083/ncomms4222-f1.jpg

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