Theoretical Investigations on the Molecular Magnetic Behavior of Actinide Molecules [AnPc2]0/- (An = U, Cf): Prediction of the High Magnetic Blocking Barrier and Magnetic Blocking Temperature in [CfPc2].

IF 2.8 2区 化学 Q3 CHEMISTRY, PHYSICAL The Journal of Physical Chemistry A Pub Date : 2025-01-23 Epub Date: 2025-01-08 DOI:10.1021/acs.jpca.4c06757
Jie Liu, Yaqing Chen, Huan Tang, Hong Chen, Ruizhi Qiu, Hongkuan Yuan
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Abstract

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 5f 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 Ueff. In combination of the density functional theory (DFT) as well as the CF model Hamiltonian and ab initio calculation, we have investigated the structural stability and electronic structures as well as the magnetodynamic behavior of [AnPc2]0/- (An = U, Cf) molecules. We find that An atoms can strongly interact with its ligand N atoms in forming An-N ionic bonds, and 5f electrons are more localized in the Cf atom than in the U atom, giving U4+(5f2) and Cf3+(5f9) valence states. Although the UPc2 molecule has a modest value of Ueff = 514 cm-1, 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 ab initio calculations on the [CfPc2]- 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 Ueff = 1401 cm-1. The estimated high magnetic blocking temperature (TB) of 58 K renders [CfPc2]- an excellent SMM candidate, implying that magnetic hysteresis could be observed in future experiments.

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锕系元素[AnPc2]0/- (An = U, Cf)分子磁性行为的理论研究:[CfPc2]中高磁阻挡势垒和磁阻挡温度的预测。
寻找具有大有效阻挡势、长弛豫时间和高磁阻挡温度的单分子磁体(SMM),不仅对分子水平的磁学基础研究,而且对新一代磁存储单元的实现具有重要意义。锕系元素(An)原子由于其5f轨道而具有极强的自旋轨道耦合(SOC),并且由于a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,它们的地面多重态在很大程度上分裂为几个亚能级。与基于tm的smm相比,基于an的smm的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Ueff提供了必要条件。结合密度泛函理论(DFT)、CF模型哈密顿量和从头计算,研究了[AnPc2]0/- (An = U, CF)分子的结构稳定性、电子结构和磁动力行为。我们发现,a原子可以与配体N原子强烈地相互作用,形成An-N离子键,并且5f电子在Cf原子中比在U原子中更集中,形成U4+(5f2)和Cf3+(5f9)价态。UPc2分子虽然具有Ueff = 514 cm-1的适中值,但由于容易发生磁化量子隧穿(QTM),它并不是一个很好的SMM。基于对[CfPc2]-分子的CF哈密顿量和从头计算的一致结果,我们提出了Kramers双重态(KDs)内几乎禁止的QTM以及通过阻碍自旋翻转跃迁在不同状态之间的极低跃迁概率将导致高Ueff = 1401 cm-1。估计58 K的高磁阻温度(TB)使[CfPc2]-成为一个优秀的SMM候选者,这意味着在未来的实验中可以观察到磁滞。
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来源期刊
The Journal of Physical Chemistry A
The Journal of Physical Chemistry A 化学-物理:原子、分子和化学物理
CiteScore
5.20
自引率
10.30%
发文量
922
审稿时长
1.3 months
期刊介绍: The Journal of Physical Chemistry A is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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