Dahal Bishnu R, Savadkoohi Marzieh, Grizzle Andrew, D'Angelo Christopher, Lamberti Vincent, Tyagi Pawan
Center for Nanotechnology Research and Education, Mechanical Engineering, University of the District of Columbia, Washington, DC, 20008, USA.
Y-12 National Security Complex, 301 Bear Creek Rd, Oak Ridge, TN, 37830, USA.
Sci Rep. 2022 Apr 6;12(1):5721. doi: 10.1038/s41598-022-09321-7.
Magnetic tunnel junction-based molecular spintronics device (MTJMSD) may enable novel magnetic metamaterials by chemically bonding magnetic molecules and ferromagnets (FM) with a vast range of magnetic anisotropy. MTJMSD have experimentally shown intriguing microscopic phenomenon such as the development of highly contrasting magnetic phases on a ferromagnetic electrode at room temperature. This paper focuses on Monte Carlo Simulations (MCS) on MTJMSD to understand the potential mechanism and explore fundamental knowledge about the impact of magnetic anisotropy. The selection of MCS is based on our prior study showing the potential of MCS in explaining experimental results (Tyagi et al. in Nanotechnology 26:305602, 2015). In this paper, MCS is carried out on the 3D Heisenberg model of cross-junction-shaped MTJMSDs. Our research represents the experimentally studied cross-junction-shaped MTJMSD where paramagnetic molecules are covalently bonded between two FM electrodes along the exposed side edges of the magnetic tunnel junction (MTJ). We have studied atomistic MTJMSDs properties by simulating a wide range of easy-axis anisotropy for the case of experimentally observed predominant molecule-induced strong antiferromagnetic coupling. Our study focused on understanding the effect of anisotropy of the FM electrodes on the overall MTJMSDs at various temperatures. This study shows that the multiple domains of opposite spins start to appear on an FM electrode as the easy-axis anisotropy increases. Interestingly, MCS results resembled the experimentally observed highly contrasted magnetic zones on the ferromagnetic electrodes of MTJMSD. The magnetic phases with starkly different spins were observed around the molecular junction on the FM electrode with high anisotropy.
基于磁隧道结的分子自旋电子器件(MTJMSD)通过将具有广泛磁各向异性的磁性分子与铁磁体(FM)化学键合,可能实现新型磁性超材料。MTJMSD在实验中已展现出有趣的微观现象,例如在室温下铁磁电极上出现高对比度的磁相。本文聚焦于对MTJMSD进行蒙特卡罗模拟(MCS),以理解潜在机制并探索有关磁各向异性影响的基础知识。选择MCS是基于我们之前的研究,该研究表明MCS在解释实验结果方面具有潜力(Tyagi等人,《纳米技术》26:305602,2015)。在本文中,对交叉结形MTJMSD的三维海森堡模型进行了MCS。我们的研究代表了对交叉结形MTJMSD的实验研究,其中顺磁分子沿着磁隧道结(MTJ)的暴露侧边共价键合在两个FM电极之间。对于实验观察到的主要分子诱导强反铁磁耦合的情况进行了模拟,我们研究了原子级MTJMSD的特性,通过模拟广泛的易轴各向异性。我们的研究重点是理解FM电极的各向异性在不同温度下对整体MTJMSD的影响。这项研究表明,随着易轴各向异性增加,FM电极上开始出现相反自旋的多个畴。有趣的是,MCS结果类似于在MTJMSD的铁磁电极上实验观察到的高对比度磁区。在具有高各向异性的FM电极上,在分子结周围观察到了自旋明显不同的磁相。