物理
近藤效应
自旋电子学
量子
密度泛函理论
联轴节(管道)
凝聚态物理
安德森杂质模型
量子点
自旋(空气动力学)
自旋态
电子结构
量子力学
自旋工程
态密度
耦合强度
共振(粒子物理)
化学
极化(电化学)
自旋极化
量子态
磁性杂质
量子动力学
分子动力学
电子顺磁共振
电子
分子
磁场
感应耦合
作者
Xiaoli Wang,Longqing Yang,Ping Wu,Xinru Zhu,Yaqin Tian,Zhen Li,Zhongmin Liu,Yuexing Zhang
摘要
The manipulation of quantum states in triple-decker organometallic molecules remains challenging due to their complex many-body interactions. In this study, we combine density functional theory (DFT) and the hierarchical equations of motion (HEOM) to map, for the first time, the evolution of quantum states in a triple-decker dinuclear complex under mechanical manipulation by a magnetic cobalt tip. DFT calculations demonstrate that the tip approach induces substantial structural distortion of the molecular framework, which triggers a reconstruction of the internal magnetic coupling network. This process is accompanied by an evolution of the electronic structure that includes modifications to the local density of states, magnetic moment, spin-state populations, and molecular orbital hybridization characteristics. By solving the spin-polarized Anderson model using the HEOM method, we have revealed the dynamic evolution of strongly correlated Kondo effects. When the system enters the contact regime, the Kondo resonance peak exhibits asymmetric splitting, where the splitting characteristics exhibit a simultaneous dependence on the spin polarization degree of the electrodes and the coupling strength between the impurity and the electrodes. These atomic-scale insights into the external control of molecular quantum states provide a robust framework for the future design of molecular spintronic devices.
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