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氢键金属有机框架中结构与多铁性的压力控制

Pressure Control of the Structure and Multiferroicity in a Hydrogen-Bonded Metal-Organic Framework.

作者信息

Zhou Houjian, Ding Hao, Yu Zhipeng, Yu Tongtong, Zhai Kun, Wang Bochong, Mu Congpu, Wen Fusheng, Xiang Jianyong, Xue Tianyu, Wang Lin, Liu Zhongyuan, Sun Young, Tian Yongjun

机构信息

Center for High Pressure Science (CHiPS), State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, China.

Center of Quantum Materials and Devices, Chongqing University, Chongqing 401331, China.

出版信息

Inorg Chem. 2022 Jun 27;61(25):9631-9637. doi: 10.1021/acs.inorgchem.2c01083. Epub 2022 Jun 13.

Abstract

Multiferroic materials with the cross-coupling of magnetic and ferroelectric orders provide a new platform for physics study and designing novel electronic devices. However, the weak coupling strength of ferroelectricity and magnetism is the main obstacle for potential applications. The recent research focuses on enhancing the coupling effect via synthesizing novel materials in a chemical route or tuning the multiferroicity in the physical way. Among them, pressure is an effective method to modify multiferroic materials, especially when the chemical doping has reached its tuning limit. In this work, we systemically studied the multiferroic properties in a hydrogen-bonded metal-organic framework (MOF) [(CH)NH]Ni(HCOO) under high pressure. X-ray diffraction and Raman scattering reveal that a structural phase transition occurs in a pressure region of 6-9 GPa, and the crystal structure is greatly modified by pressure. With the ac magnetic susceptibility, pyroelectric current, and dielectric constant measurements, we obtain the multiferroic property evolution under high pressure and create a temperature-pressure phase diagram. Our study demonstrates that the pressure can modify the magnetic superexchange interaction and hydrogen bonding simultaneously in these perovskite-like MOFs. The multiferroic phase region has been expanded to higher temperature due to the pressure-enhanced spin-phonon coupling effect.

摘要

具有磁序和铁电序交叉耦合的多铁性材料为物理研究和设计新型电子器件提供了一个新平台。然而,铁电性与磁性之间较弱的耦合强度是其潜在应用的主要障碍。最近的研究集中在通过化学途径合成新型材料或以物理方式调节多铁性来增强耦合效应。其中,压力是一种修饰多铁性材料的有效方法,尤其是在化学掺杂已达到其调节极限时。在这项工作中,我们系统地研究了高压下氢键金属有机框架(MOF)[(CH)NH]Ni(HCOO)中的多铁性性质。X射线衍射和拉曼散射表明,在6-9 GPa的压力区域发生了结构相变,并且晶体结构因压力而发生了很大改变。通过交流磁化率、热电流和介电常数测量,我们获得了高压下的多铁性性质演变并创建了温度-压力相图。我们的研究表明,压力可以同时改变这些类钙钛矿MOF中的磁超交换相互作用和氢键。由于压力增强的自旋-声子耦合效应多铁性相区域已扩展到更高温度。

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