Liu Jie, Chen Yaqing, Tang Huan, Chen Hong, Qiu Ruizhi, Yuan Hongkuan
School of Physical Science and Technology, Southwest University, Chongqing 400715, China.
Institute of Materials, China Academy of Engineering Physics, Mianyang, Sichuan 621907, China.
J Phys Chem A. 2025 Jan 23;129(3):717-732. doi: 10.1021/acs.jpca.4c06757. Epub 2025 Jan 8.
Searching for single-molecule magnets (SMM) with large effective blocking barriers, long relaxation times, and high magnetic blocking temperatures is vitally important not only for the fundamental research of magnetism at the molecular level but also for the realization of new-generation magnetic memory unit. Actinides (An) atoms possess extremely strong spin-orbit coupling (SOC) due to their 5 orbitals, and their ground multiplets are largely split into several sublevels because of the strong interplay between the SOC of An atoms and the crystal field (CF) formed by ligand atoms. Compared to TM-based SMMs, more dispersed energy level widths of An-based SMMs will give a larger total zero field splitting (ZFS) and thus provide a necessary condition to derive a higher . In combination of the density functional theory (DFT) as well as the CF model Hamiltonian and calculation, we have investigated the structural stability and electronic structures as well as the magnetodynamic behavior of [AnPc] (An = U, Cf) molecules. We find that An atoms can strongly interact with its ligand N atoms in forming An-N ionic bonds, and 5 electrons are more localized in the Cf atom than in the U atom, giving U(5f) and Cf(5f) valence states. Although the UPc molecule has a modest value of = 514 cm, it is not a good SMM due to the easy occurrence of quantum tunneling of magnetization (QTM). Based on the consistent results of CF Hamiltonian and calculations on the [CfPc] molecule, we propose that almost prohibited QTM within the Kramers doublets (KDs) as well as very low transition probabilities between different states via hindered spin-flip transitions would result in a high = 1401 cm. The estimated high magnetic blocking temperature () of 58 K renders [CfPc] an excellent SMM candidate, implying that magnetic hysteresis could be observed in future experiments.
寻找具有大有效阻挡势垒、长弛豫时间和高磁阻挡温度的单分子磁体(SMM)不仅对分子水平上的磁性基础研究至关重要,而且对新一代磁存储单元的实现也至关重要。锕系(An)原子由于其5个轨道而具有极强的自旋轨道耦合(SOC),并且由于An原子的SOC与配体原子形成的晶体场(CF)之间的强烈相互作用,它们的基多重态在很大程度上分裂为几个子能级。与基于过渡金属(TM)的SMM相比,基于An的SMM更分散的能级宽度将产生更大的总零场分裂(ZFS),从而为获得更高的[具体物理量,原文未明确给出]提供必要条件。结合密度泛函理论(DFT)以及CF模型哈密顿量和[具体计算方法,原文未明确给出]计算,我们研究了[AnPc](An = U,Cf)分子的结构稳定性、电子结构以及磁动力学行为。我们发现An原子在形成An-N离子键时能与其配体N原子强烈相互作用,并且5个电子在Cf原子中比在U原子中更局域化,给出U(5f)和Cf(5f)价态。尽管UPc分子的[具体物理量,原文未明确给出]值适中,为514 cm,但由于磁化量子隧穿(QTM)容易发生,它不是一个好的SMM。基于对[CfPc]分子的CF哈密顿量和[具体计算方法,原文未明确给出]计算的一致结果,我们提出在克莱默斯双态(KDs)内几乎被禁止的QTM以及通过受阻自旋翻转跃迁在不同状态之间非常低的跃迁概率将导致高的[具体物理量,原文未明确给出]值为1401 cm。估计的58 K的高磁阻挡温度([具体物理量,原文未明确给出])使[CfPc]成为一个优秀的SMM候选物,这意味着在未来的实验中可能会观察到磁滞现象。