Treichel Marten, Möller Jenny, Meng Xiangzhi, Gutzeit Florian, Herges Rainer, Berndt Richard, Weismann Alexander
Institut für Experimentelle und Angewandte Physik, Christian-Albrechts-Universität zu Kiel, 24098 Kiel, Germany.
Otto-Diels-Institut für Organische Chemie, Christian-Albrechts-Universität zu Kiel, 24098 Kiel, Germany.
ACS Nano. 2024 Sep 14;18(38):26184-91. doi: 10.1021/acsnano.4c07477.
A complex based on a Ni(II) porphyrin exhibiting spin crossover on Ag(111) is studied on Pb(100) by scanning tunneling microscopy at 0.3 K. Strong molecular interactions between the phenyl and pentafluorophenyl moieties lead to the formation of molecular chains and cause a faceting of the substrate surface. The chains are located along double and multiple substrate steps that deviate from high-symmetry directions. Tunneling spectroscopy reveals spin-flip excitations of an = 1 system. Measurements in high magnetic fields are used to identify a tilt of the complex and its hard anisotropy axis with respect to the surface normal. Electron injection into the substrate near the molecular rows induces a transition to a state with larger inelastic cross section, leaving the spin state unchanged.
通过扫描隧道显微镜在0.3 K温度下对基于在Ag(111)上表现出自旋交叉的Ni(II)卟啉的配合物在Pb(100)上进行了研究。苯基和五氟苯基部分之间的强分子相互作用导致分子链的形成,并使衬底表面出现刻面。这些链沿着偏离高对称方向的双台阶和多台阶排列。隧道光谱揭示了S = 1体系的自旋翻转激发。在高磁场中的测量用于确定配合物相对于表面法线的倾斜及其硬各向异性轴。在分子行附近向衬底注入电子会诱导向具有更大非弹性截面的状态转变,而自旋状态保持不变。