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室温下钒掺杂二硒化钨单层中的可调铁磁性和热致自旋翻转

Tunable Ferromagnetism and Thermally Induced Spin Flip in Vanadium-Doped Tungsten Diselenide Monolayers at Room Temperature.

作者信息

Pham Yen Thi Hai, Liu Mingzu, Jimenez Valery Ortiz, Yu Zhuohang, Kalappattil Vijaysankar, Zhang Fu, Wang Ke, Williams Teague, Terrones Mauricio, Phan Manh-Huong

机构信息

Department of Physics, University of South Florida, Tampa, FL, 33620, USA.

Department of Physics, The Pennsylvania State University, University Park, PA, 16802, USA.

出版信息

Adv Mater. 2020 Nov;32(45):e2003607. doi: 10.1002/adma.202003607. Epub 2020 Oct 5.

DOI:10.1002/adma.202003607
PMID:33015889
Abstract

The outstanding optoelectronic and valleytronic properties of transition metal dichalcogenides (TMDs) have triggered intense research efforts by the scientific community. An alternative to induce long-range ferromagnetism (FM) in TMDs is by introducing magnetic dopants to form a dilute magnetic semiconductor. Enhancing ferromagnetism in these semiconductors not only represents a key step toward modern TMD-based spintronics, but also enables exploration of new and exciting dimensionality-driven magnetic phenomena. To this end, tunable ferromagnetism at room temperature and a thermally induced spin flip (TISF) in monolayers of V-doped WSe are shown. As vanadium concentration increases, the saturation magnetization increases, which is optimal at ≈4 at% vanadium; the highest doping level ever achieved for V-doped WSe monolayers. The TISF occurs at ≈175 K and becomes more pronounced upon increasing the temperature toward room temperature. The TISF can be manipulated by changing the vanadium concentration. The TISF is attributed to the magnetic-field- and temperature-dependent flipping of the nearest W-site magnetic moments that are antiferromagnetically coupled to the V magnetic moments in the ground state. This is fully supported by a recent spin-polarized density functional theory study. The findings pave the way for the development of novel spintronic and valleytronic nanodevices and stimulate further research.

摘要

过渡金属二硫属化物(TMDs)优异的光电和谷电子特性引发了科学界的广泛研究。在TMDs中诱导长程铁磁性(FM)的一种方法是引入磁性掺杂剂以形成稀磁半导体。增强这些半导体中的铁磁性不仅是迈向基于TMD的现代自旋电子学的关键一步,还能够探索新的、令人兴奋的维度驱动磁现象。为此,展示了在V掺杂的WSe单层中室温下的可调铁磁性和热诱导自旋翻转(TISF)。随着钒浓度的增加,饱和磁化强度增加,在钒含量约为4 at%时达到最佳;这是V掺杂WSe单层迄今实现的最高掺杂水平。TISF发生在约175 K,并随着温度升高至室温而变得更加明显。TISF可以通过改变钒浓度来操控。TISF归因于与基态V磁矩反铁磁耦合的最近W位磁矩的磁场和温度依赖性翻转。这得到了最近一项自旋极化密度泛函理论研究的充分支持。这些发现为新型自旋电子和谷电子纳米器件的开发铺平了道路,并激发了进一步的研究。

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