A cation-exchange approach to tunable magnetic intercalation superlattices.

IF 50.5 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Nature Pub Date : 2025-06-25 DOI:10.1038/s41586-025-09147-z
Jingxuan Zhou,Jingyuan Zhou,Zhong Wan,Qi Qian,Huaying Ren,Xingxu Yan,Boxuan Zhou,Ao Zhang,Xiaoqing Pan,Wuzhang Fang,Yuan Ping,Zdenek Sofer,Yu Huang,Xiangfeng Duan
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Abstract

Tailoring magnetic ordering in solid-state materials is essential for emerging spintronics1,2. However, substitutional lattice doping in magnetic semiconductors is often constrained by the low solubility of magnetic elements3-5, limiting the maximum achievable doping concentration (for example, less than 5%) and ferromagnetic ordering temperature6. The intercalation of magnetic elements in layered two-dimensional atomic crystals (2DACs) without breaking in-plane covalent bonds offers an alternative approach to incorporate a much higher concentration of magnetic atoms (for example, up to 50%) beyond the typical solubility limit. However, commonly used chemical and electrochemical intercalation methods are largely confined to a few isolated examples so far. Here we report a general two-step intercalation and cation-exchange strategy to produce a library of highly ordered magnetic intercalation superlattices (MISLs) with tunable magnetic ordering. Monovalent transition-metal cations Cu+ and Ag+, divalent magnetic cations Mn2+, Fe2+, Co2+ and Ni2+, and trivalent rare-earth cations Eu3+ and Gd3+ have been successfully incorporated into group-VIB 2DACs, including MoS2, MoSe2, MoTe2, WS2, WSe2 and WTe2, and group-IVB, -VB, -IIIA, -IVA and -VA 2DACs, including TiS2, NbS2, NbSe2, TaS2, In2Se3, SnSe2, Bi2Se3 and Bi2Te3. We show that these MISLs can be prepared with tunable concentrations of magnetic intercalants, enabling tailored magnetic ordering across a diverse array of functional 2DACs, including semiconductors, topological insulators, and superconductors. This work establishes a versatile material platform for both fundamental investigations and spintronics applications.
可调谐磁插层超晶格的阳离子交换方法。
在固态材料中调整磁性排序对于新兴的自旋电子学至关重要1,2。然而,磁性半导体中的取代晶格掺杂通常受到磁性元素溶解度低的限制[3-5],限制了可实现的最大掺杂浓度(例如小于5%)和铁磁有序温度[6]。磁性元素在层状二维原子晶体(2dac)中嵌入而不破坏面内共价键,提供了一种替代方法,可以结合更高浓度的磁性原子(例如,高达50%),超过典型的溶解度限制。然而,目前常用的化学和电化学插层方法主要局限于少数孤立的例子。在这里,我们报告了一种一般的两步嵌入和阳离子交换策略,以产生具有可调谐磁有序的高有序磁嵌入超晶格库。已成功将一价过渡金属阳离子Cu+、Ag+、二价磁性阳离子Mn2+、Fe2+、Co2+、Ni2+、三价稀土阳离子Eu3+、Gd3+加入到vib族2DACs中,包括MoS2、MoSe2、MoTe2、WS2、WSe2和WTe2,以及ivb、-VB、-IIIA、-IVA和-VA族2DACs中,包括TiS2、NbS2、NbSe2、TaS2、In2Se3、SnSe2、Bi2Se3和Bi2Te3。我们表明,这些misl可以用可调浓度的磁性插入剂制备,从而在各种功能2dac(包括半导体、拓扑绝缘体和超导体)上实现定制的磁性排序。这项工作为基础研究和自旋电子学应用建立了一个通用的材料平台。
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
Nature
Nature 综合性期刊-综合性期刊
CiteScore
90.00
自引率
1.20%
发文量
3652
审稿时长
3 months
期刊介绍: Nature is a prestigious international journal that publishes peer-reviewed research in various scientific and technological fields. The selection of articles is based on criteria such as originality, importance, interdisciplinary relevance, timeliness, accessibility, elegance, and surprising conclusions. In addition to showcasing significant scientific advances, Nature delivers rapid, authoritative, insightful news, and interpretation of current and upcoming trends impacting science, scientists, and the broader public. The journal serves a dual purpose: firstly, to promptly share noteworthy scientific advances and foster discussions among scientists, and secondly, to ensure the swift dissemination of scientific results globally, emphasizing their significance for knowledge, culture, and daily life.
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