Hou Jie, Wang Yu, Eguchi Keitaro, Nanjo Chihiro, Takaoka Tsuyoshi, Sainoo Yasuyuki, Arafune Ryuichi, Awaga Kunio, Komeda Tadahiro
Department of Chemistry, Graduate School of Science, Tohoku University, Aramaki-Aza-AobaAoba-Ku, Sendai, 980-8578, Japan.
Institute of Multidisciplinary Research for Advanced Materials (IMRAM, Tagen), Tohoku University, 2-1-1 KatahiraAoba-Ku, Sendai, 980-0877, Japan.
Commun Chem. 2020 Mar 20;3(1):36. doi: 10.1038/s42004-020-0282-5.
Magnetic molecules are of interest for application in spintronic and quantum-information processing devices. Therein, control of the interaction between the spins of neighboring molecules is the critical issue. Substitution of outer moieties of the molecule can tune the molecule-molecule interaction. Here we show a novel spin behavior for a magnetic molecule of vanadyl tetrakis (thiadiazole) porphyrazine (abbreviated as VOTTDPz) adsorbed on Au(111), which is modified from vanadyl phthalocyanine (VOPc) by replacing the inert phthalocyanine ligand with a reactive thiadiazole moiety. The magnetic properties of the molecules are examined by observing the Kondo resonance caused by the screening of an isolated spin by conduction electrons using scanning tunneling spectroscopy. The Kondo features are detected at the molecule whose shape and intensity show site-dependent variation, revealing complex spin-spin interactions due to the enhanced interaction between molecules, originating from the functionalization of the ligand with a more reactive moiety.
磁性分子在自旋电子学和量子信息处理设备中的应用备受关注。其中,控制相邻分子自旋之间的相互作用是关键问题。分子外部基团的取代可以调节分子间相互作用。在此,我们展示了吸附在Au(111)上的钒氧基四(噻二唑)卟啉嗪(简称为VOTTDPz)磁性分子的一种新型自旋行为,它是由钒氧基酞菁(VOPc)通过用活性噻二唑基团取代惰性酞菁配体而改性得到的。利用扫描隧道谱通过观察传导电子对孤立自旋的屏蔽所引起的近藤共振来研究分子的磁性。在分子处检测到近藤特征,其形状和强度呈现出与位置有关的变化,揭示了由于分子间相互作用增强而导致的复杂自旋-自旋相互作用,这种增强源于配体被更具反应性的基团功能化。