Gálico Diogo A, Rodrigues Emille M, Halimi Ilias, Toivola Juho, Zhao He, Xu Jiahui, Moilanen Jani O, Liu Xiaogang, Hemmer Eva, Murugesu Muralee
Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, ON, K1N 6N5, Canada.
Department of Chemistry, Nanoscience Centre, University of Jyväskylä, P.O. Box 35, FI-40014, Jyväskylä, Finland.
Nat Commun. 2024 Apr 25;15(1):3498. doi: 10.1038/s41467-024-47682-x.
Molecular systems known as single-molecule magnets (SMMs) exhibit magnet-like behaviour of slow relaxation of the magnetisation and magnetic hysteresis and have potential application in high-density memory storage or quantum computing. Often, their intrinsic magnetic properties are plagued by low-energy molecular vibrations that lead to phonon-induced relaxation processes, however, there is no straightforward synthetic approach for molecular systems that would lead to a small amount of low-energy vibrations and low phonon density of states at the spin-resonance energies. In this work, we apply knowledge accumulated over the last decade in molecular magnetism to nanoparticles, incorporating Er ions in an ultrasmall sub-3 nm diamagnetic NaYF nanoparticle (NP) and probing the slow relaxation dynamics intrinsic to the Er ion. Furthermore, by increasing the doping concentration, we also investigate the role of intraparticle interactions within the NP. The knowledge gained from this study is anticipated to enable better design of magnetically high-performance molecular and bulk magnets for a wide variety of applications, such as molecular electronics.
被称为单分子磁体(SMMs)的分子系统表现出磁化强度缓慢弛豫和磁滞的类似磁行为,并且在高密度存储器存储或量子计算方面具有潜在应用。通常,它们的固有磁性能受到低能分子振动的困扰,这些振动会导致声子诱导的弛豫过程,然而,对于分子系统而言,不存在一种直接的合成方法能够在自旋共振能量下产生少量的低能振动和低声子态密度。在这项工作中,我们将过去十年在分子磁学中积累的知识应用于纳米颗粒,将铒离子掺入直径小于3nm的超小反磁性NaYF纳米颗粒(NP)中,并探究铒离子固有的缓慢弛豫动力学。此外,通过增加掺杂浓度,我们还研究了纳米颗粒内颗粒间相互作用的作用。预计从这项研究中获得的知识将有助于更好地设计用于诸如分子电子学等各种应用的磁高性能分子磁体和块体磁体。