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室温铁磁超薄α-MoO₃:Te纳米片

Room-Temperature Ferromagnetic Ultrathin α-MoO:Te Nanoflakes.

作者信息

Lee Dong Jin, Lee Youngmin, Kwon Young H, Choi Soo Ho, Yang Woochul, Kim Deuk Young, Lee Sejoon

机构信息

Quantum-functional Semiconductor Research Center , Dongguk University - Seoul 04623 , Korea.

Department of Physics , Dongguk University - Seoul 04623 , Korea.

出版信息

ACS Nano. 2019 Aug 27;13(8):8717-8724. doi: 10.1021/acsnano.9b01179. Epub 2019 Jul 15.

Abstract

We materialized room-temperature ferromagnetism in ultrathin α-MoO:Te nanoflakes. The α-MoO:Te nanoflakes, which had been grown by vapor-phase epitaxy, clearly exhibited an A Raman band from symmetric stretching of υ(Mo-O-Mo) in the 2D-like ultrathin α-MoO:Te layer. Due to the intentional incorporation of smaller Te ions into bigger Mo sites, the pentacoordinated Mo bonds were created inside the orthorhombic α-MoO:Te lattice system. Since Mo ions have magnetic moments from unpaired electron spins, a large number of overlapped bound magnetic polarons could be formed ferromagnetic coupling with charged oxygen vacancies that are inevitably generated at pentacoordinated [MoO] centers. This gives rise to the increase in long-range ferromagnetic ordering and leads to room-temperature ferromagnetism in the entire α-MoO:Te solid-state system. The results may move a step closer to the demonstration of spin functionalities in the wide bandgap semiconductor α-MoO:Te.

摘要

我们在超薄α-MoO₃:Te纳米片中实现了室温铁磁性。通过气相外延生长的α-MoO₃:Te纳米片,在类二维超薄α-MoO₃:Te层中,由υ(Mo-O-Mo)的对称伸缩产生的A拉曼带清晰可见。由于有意将较小的Te离子掺入较大的Mo位点,在正交晶系α-MoO₃:Te晶格系统内部形成了五配位的Mo键。由于Mo离子具有未成对电子自旋产生的磁矩,大量重叠的束缚磁极化子可与在五配位[MoO]中心不可避免产生的带电氧空位形成铁磁耦合。这导致长程铁磁有序性增加,并在整个α-MoO₃:Te固态系统中产生室温铁磁性。这些结果可能使我们更接近在宽带隙半导体α-MoO₃:Te中展示自旋功能。

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