铷
晶体结构
磁矩
材料科学
反铁磁性
拉曼光谱
插层(化学)
顺磁性
碱金属
结晶学
铁磁性
Crystal(编程语言)
居里温度
凝聚态物理
化学
金属
抗磁性
核磁共振
电子顺磁共振
分子振动
单晶
电子
作者
Xiaolin Wu,Hui Yang,Mingan Fu,Shan Peng,Yang Liu,Chuanyang Zhao,Debing Long,Yun Gao,Zhongbing Huang
出处
期刊:ACS omega
[American Chemical Society]
日期:2026-01-20
卷期号:11 (4): 6014-6022
标识
DOI:10.1021/acsomega.5c10344
摘要
Intercalation of alkali metals into aromatic hydrocarbons offers significant potential for achieving organic magnetism. In this study, rubidium-intercalated 2-phenylnaphthalene molecular crystals were synthesized successfully by ultrasonic treatment and low-temperature annealing. Magnetic measurements demonstrate that the rubidium-intercalated samples exhibit typical Curie paramagnetism with a molar magnetic moment of approximately 0.44 μB. XRD and Raman spectroscopy measurements confirm that the structure and vibration information on the prepared samples differ from those of pristine 2-phenylnaphthalene, indicating that a new structure is formed by intercalating preparation. First-principles calculations yield optimized theoretical structures and magnetic moments that align with experimental observations, suggesting that Rb-5s electrons from intercalated rubidium are transferred to the C-2p orbitals of the organic molecules. Upon application of pressure, the intercalated crystal is predicted to transit from an antiferromagnetic to a nonmagnetic metallic state. These findings demonstrate that introducing rubidium atoms with strong reducing ability into aromatic hydrocarbons provides new opportunities for developing the magnetic properties of these materials.
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