Spatial engineering of molecular spin states with atomic precision is essential for emerging molecule-based quantum devices. This requires both atomic-scale manipulations of molecules and a deep understanding of magnetic interactions. Here, we demonstrate significant spin redistribution in an iron(II)-phthalocyanine (FePc) molecule modified by adding an Fe atom to one of its lobes, thereby forming an FePc(Fe) complex. The formation of FePc(Fe) complexes leads to a redistribution of the spin density from the constituent units. We directly probe this distribution using an electron spin resonance implemented in a scanning tunneling microscope and individual titanium atoms as sensors. This reveals a pronounced asymmetric molecular spin distribution that is enhanced at the lobe with added Fe and reduced at the central Fe, as supported by theoretical calculations. Our findings shed light on metal atom doping as an effective approach for chemically engineering the spatial symmetry of molecular spin states and tuning magnetic interactions in surface-supported molecular spin architectures.
Wu et al. (Thu,) studied this question.