Mier Cristina, Verlhac Benjamin, Garnier Léo, Robles Roberto, Limot Laurent, Lorente Nicolás, Choi Deung-Jang
Centro de Física de Materiales CFM/MPC (CSIC-UPV/EHU), 20018 Donostia-San Sebastián, Spain.
Université de Strasbourg CNRS, IPCMS, UMR 7504, F-67000 Strasbourg, France.
J Phys Chem Lett. 2021 Mar 25;12(11):2983-2989. doi: 10.1021/acs.jpclett.1c00328. Epub 2021 Mar 17.
Combining the complex ordering ability of molecules with their local magnetic properties is a little-explored technique to tailor spin structures on surfaces. However, revealing the molecular geometry can be demanding. Nickelocene (Nc) molecules present a large spin-flip excitation leading to clear changes of conductance at the excitation-threshold bias. Using a superconducting tip, we have the energy resolution to detect small shifts of the Nc spin-flip excitation thresholds, permitting us to reveal the different individual environments of Nc molecules in an ordered layer. This knowledge allows us to reveal the adsorption configuration of a complex molecular structure formed by Nc molecules in different orientations and positions. As a consequence, we infer that Nc layers present a strong noncollinear magnetic-moment arrangement.
将分子的复杂有序能力与其局部磁性相结合,是一种用于在表面定制自旋结构但鲜少被探索的技术。然而,揭示分子几何结构可能具有挑战性。二茂镍(Nc)分子呈现出较大的自旋翻转激发,导致在激发阈值偏压下电导发生明显变化。使用超导尖端,我们具备检测Nc自旋翻转激发阈值微小偏移的能量分辨率,从而能够揭示有序层中Nc分子的不同个体环境。这一知识使我们得以揭示由处于不同取向和位置的Nc分子形成复杂分子结构的吸附构型。因此,我们推断Nc层呈现出强烈的非共线磁矩排列。