4.6 Article

Understanding the Sub-meV Precision-Tuning of Magnetic Anisotropy of Single-Molecule Junction

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 125, Issue 12, Pages 6990-6997

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.1c01398

Keywords

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Funding

  1. Ministry of Science and Technology of China [2016YFA0400900, 2016YFA0200600]
  2. National Natural Science Foundation of China [21973086, 21633006]
  3. Fundamental Research Funds for the Central Universities [WK2060000018]

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The high-precision fine-tuning of the magnetic anisotropy energy (MAE) of a magnetic molecule using a scanning tunneling microscope (STM) tip has been experimentally demonstrated. The study reveals the crucial influence of the surrounding environment on the molecular spin state and provides insights into the exotic evolution of MAE attributed to ligand confinement effect and charge transfer. The theoretical understanding obtained from this work is valuable for the design of mechanically controlled magnetic nanojunctions.
Fine-tuning the magnetic anisotropy energy (MAE) of a magnetic molecule with a high precision of sub-meV has been realized experimentally by manipulating the tip of a scanning tunneling microscope (STM). Understanding the mechanisms behind the observed evolution of spin excitation energy is essentially important for potential spintronic applications. In particular, it is crucial to unveil the influence of the surrounding environment on the molecular spin state. To this end, we carry out the first-principles simulation on the STM-tip control of an iron octaethylporphyrin chloride (Fe-OEP-Cl) molecule adsorbed on the Pb(111) substrate. By carefully taking into account the atomic structures of the tip and the substrate as well as the multireference feature of the Fe 3d electrons, the experimentally measured evolution of spin excitation energy, including a continuous increase, followed by a sudden drop in the MAE, is accurately reproduced by our simulation with a maximal discrepancy of less than 0.3 meV. Based on a comprehensive analysis of the change in geometric and electronic structures of the whole single-molecule junction, the exotic evolution of MAE is attributed to the variation of the ligand confinement effect and the resulting charge transfer. The unique role of the single-atomic Cl ligand is clarified by comparing the evolution under the STM-tip control with that of the tip/Fe-OEP/Pb(111) junction. The theoretical insights provided by this work would be valuable for the on-demand design of the mechanically controlled magnetic nanojunctions.

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