居里温度
超级交换
吡嗪
磁性
铁磁性
化学
磁铁
金属有机骨架
自旋电子学
铁磁性
材料科学
结晶学
磁化
离子
无机化学
物理化学
凝聚态物理
吸附
立体化学
有机化学
物理
磁场
量子力学
作者
Haifeng Lv,Xiangyang Li,Daoxiong Wu,Ying Liu,Xingxing Li,Xiaojun Wu,Jinlong Yang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-02-11
卷期号:22 (4): 1573-1579
被引量:31
标识
DOI:10.1021/acs.nanolett.1c04398
摘要
Two-dimensional (2D) metal-organic frameworks (MOFs) with room-temperature magnetism are highly desirable but challenging due to the weak superexchange interaction between metal atoms. For this purpose, strengthening the hybridization between metal ion and organic linkage presents an experiment-feasible chemical solution to enhance the Curie temperature. Here, we report three 2D Cr(II) aromatic heterocyclic MOF magnets with enhanced Curie temperature by bridging Cr(II) ions with pyrazine, 1,4-diphosphinine, and 1,4-diarsenin linkers, i.e., Cr(pyz)2, Cr(diphos)2, and Cr(diarse)2, and using first-principles calculations. Our results show that Cr(pyz)2, Cr(diphos)2, and Cr(diarse)2 are ferrimagnetic semiconductors. In particular, the Curie temperature of Cr(pyz)2 is estimated to be about 344 K and could be enhanced to 512 and 437 K in Cr(diphos)2 and Cr(diarse)2 by strengthening the hybridization between Cr ions and organic linkers via d-π* direct exchange interaction. This study presents a prototype to obtain room-temperature magnetism in 2D Cr(II)-based MOF magnets for nanoscale spintronics applications.
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