Institut für Experimentalphysik, Freie Universität Berlin, 14195 Berlin, Germany.
Phys Rev Lett. 2012 Oct 5;109(14):147202. doi: 10.1103/PhysRevLett.109.147202. Epub 2012 Oct 2.
We show that the magnetic state of individual manganese phthalocyanine (MnPc) molecules on a Bi(110) surface is modified when the Mn2+ center coordinates to CO molecules adsorbed on top. Using scanning tunneling spectroscopy we identified this change in magnetic properties from the broadening of a Kondo-related zero-bias anomaly when the CO-MnPc complex is formed. The original magnetic state can be recovered by selective desorption of individual CO molecules. First principles calculations show that the CO molecule reduces the spin of the adsorbed MnPc from S=1 to S=1/2 and strongly modifies the respective screening channels, driving a transition from an underscreened Kondo state to a state of mixed valence.
我们表明,当 Mn2+ 中心与吸附在顶部的 CO 分子配位时,单个锰酞菁(MnPc)分子在 Bi(110) 表面上的磁态会发生变化。通过扫描隧道光谱学,我们发现当 CO-MnPc 复合物形成时,Kondo 相关零偏压异常的展宽导致了这种磁性质的变化。通过选择性解吸单个 CO 分子可以恢复原始的磁状态。第一性原理计算表明,CO 分子将吸附的 MnPc 的自旋从 S=1 降低到 S=1/2,并强烈改变各自的屏蔽通道,导致从欠屏蔽的 Kondo 态到混合价态的转变。