Studniarek Michał, Wäckerlin Christian, Singha Aparajita, Baltic Romana, Diller Katharina, Donati Fabio, Rusponi Stefano, Brune Harald, Lan Yanhua, Klyatskaya Svetlana, Ruben Mario, Seitsonen Ari Paavo, Dreiser Jan
Swiss Light Source Paul Scherrer Institut (PSI) CH-5232 Villigen Switzerland.
Institute of Physics (IPHYS) École Polytechnique Fédérale de Lausanne (EPFL) Station 3 CH-1015 Lausanne Switzerland.
Adv Sci (Weinh). 2019 Sep 30;6(22):1901736. doi: 10.1002/advs.201901736. eCollection 2019 Nov.
The stability of magnetic information stored in surface adsorbed single-molecule magnets is of critical interest for applications in nanoscale data storage or quantum computing. The present study combines X-ray magnetic circular dichroism, density functional theory and magnetization dynamics calculations to gain deep insight into the substrate dependent relevant magnetization relaxation mechanisms. X-ray magnetic circular dichroism reveals the opening of a butterfly-shaped magnetic hysteresis of DyPc molecules on magnesium oxide and a closed loop on the bare silver substrate, while density functional theory shows that the molecules are only weakly adsorbed in both cases of magnesium oxide and silver. The enhanced magnetic stability of DyPc on the oxide film, in conjunction with previous experiments on the TbPc analogue, points to a general validity of the magnesium oxide induced stabilization effect. Magnetization dynamics calculations reveal that the enhanced magnetic stability of DyPc and TbPc on the oxide film is due to the suppression of two-phonon Raman relaxation processes. The results suggest that substrates with low phonon density of states are beneficial for the design of spintronics devices based on single-molecule magnets.
存储在表面吸附单分子磁体中的磁信息稳定性对于纳米级数据存储或量子计算应用至关重要。本研究结合了X射线磁性圆二色性、密度泛函理论和磁化动力学计算,以深入了解与衬底相关的相关磁化弛豫机制。X射线磁性圆二色性揭示了DyPc分子在氧化镁上呈现蝴蝶形磁滞回线的开启以及在裸银衬底上呈现闭合回线,而密度泛函理论表明分子在氧化镁和银这两种情况下都只是弱吸附。DyPc在氧化膜上增强的磁稳定性,结合之前对TbPc类似物的实验,表明氧化镁诱导的稳定效应具有普遍有效性。磁化动力学计算表明,DyPc和TbPc在氧化膜上增强的磁稳定性是由于双声子拉曼弛豫过程受到抑制。结果表明,具有低声子态密度的衬底有利于基于单分子磁体的自旋电子器件的设计。