Artificial Room-Temperature Ferromagnetism of Bulk van der Waals VSe2

IF 14.1 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jinhyoung Lee, Gunhyoung Kim, Hyunho Seok, Hyunbin Choi, Hyeonjeong Lee, Seokchan Lee, Geonwook Kim, Hyunho Kim, Seowoo Son, Sihoon Son, Dongho Lee, Hosin Hwang, Hyelim Shin, Sujeong Han, Geumji Back, Alexina Ollier, Yeon-Ji Kim, Lei Fang, Gyuho Han, Goo-Eun Jung, Youngi Lee, Hyeong-U Kim, Kenji Watanabe, Takashi Taniguchi, Wonjun Shin, Suraj Cheema, Andreas Heinrich, Won-Jun Jang, Taesung Kim
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Abstract

Originating from spin and orbital motion, van der Waals (vdW) ferromagnetism has emerged as a significant platform to experimentally access the fundamental physics of magnetism in reduced dimensions, including quantum computing, sensing, and data storage. However, currently, available vdW ferromagnetic materials can be achieved with mechanical exfoliation and low-temperature operation, which completely limits the monolithic integration of vdW ferromagnets with other functional materials. Nonetheless, the direct synthesis of room-temperature vdW ferromagnets has not been achieved commercially, owing to the imprecise control of the layer-by-layer growth, high-temperature synthesis, and low yield. To overcome these limitations, herein, an artificial vdW ferromagnetic platform has been reported, which activates the nano-crystallization and its corresponding ferromagnetism in bulk VSe2 via Ar + H2S plasma sulfurization. Sweeping the magnetic field, vdW ferromagnetism has been spatially resolved, which experimentally correlates with magnetization reversal behavior and domain pinning effects. Furthermore, nano-crystallization of VSe2 is clearly validated with transmission electron microscopy, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and selected area diffraction analysis. In conclusion, it is envisioned that the artificial vdW ferromagnetic platform can artificially inject the ferromagnetism in bulk vdW VSe2, which has not been possible previously.

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体范德华VSe2的人工室温铁磁性。
范德华铁磁性(vdW)起源于自旋和轨道运动,已经成为一个重要的实验平台,可以在降维中访问磁性的基本物理,包括量子计算,传感和数据存储。然而,目前可用的vdW铁磁材料可以通过机械剥离和低温操作来实现,这完全限制了vdW铁磁材料与其他功能材料的单片集成。然而,直接合成室温vdW铁磁体尚未实现商业化,原因是对逐层生长的控制不精确,合成温度高,产率低。为了克服这些限制,本文报道了一种人工vdW铁磁性平台,该平台通过Ar + H2S等离子体硫化激活了块状VSe2的纳米结晶及其相应的铁磁性。扫描磁场,对vdW铁磁性进行了空间解析,实验结果表明,vdW铁磁性与磁化反转行为和畴钉钉效应有关。此外,通过透射电镜、能量色散x射线能谱、x射线光电子能谱和选择区域衍射分析,明确验证了VSe2的纳米结晶。综上所述,我们设想人工vdW铁磁平台可以人为地将铁磁性注入到块状vdW VSe2中,这是以前无法实现的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advanced Science
Advanced Science CHEMISTRY, MULTIDISCIPLINARYNANOSCIENCE &-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
18.90
自引率
2.60%
发文量
1602
审稿时长
1.9 months
期刊介绍: Advanced Science is a prestigious open access journal that focuses on interdisciplinary research in materials science, physics, chemistry, medical and life sciences, and engineering. The journal aims to promote cutting-edge research by employing a rigorous and impartial review process. It is committed to presenting research articles with the highest quality production standards, ensuring maximum accessibility of top scientific findings. With its vibrant and innovative publication platform, Advanced Science seeks to revolutionize the dissemination and organization of scientific knowledge.
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