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The Effect of Adsorbed Molecules on Electronic Structure and Magnetic Properties of Nanographites

机译:吸附分子对纳米型电子结构和磁性特性的影响

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The results of investigation of changes in electronic structure and magnetic properties of multilayer graphene nanoclusters (nanographites) occurring during their interaction with adsorbed chlorine molecules are presented. The found reversible decrease in the density of states of current carriers D(E_F) at the Fermi energy E_F can be explained by the spin-splitting of edge π-electron states in nanographites induced by the enhancement of electron-electron interactions due to increase of the D(E_F) at partial transfer of the electron density from nanographites to chlorine adatoms. The revealed irreversible decrease in the concentration of localized spins indicates that the electron spins of 3p-orbitals of chlorine and unpaired (dundling) σ-orbitals of edge carbon atoms are coupled also at this interaction, i.e. the edge covalent compound of nanographite with chlorine forms. Character of changes in the spin-relaxation rate of π-electrons depending on the amount of adsorbed chlorine molecules and on temperature in chlorinated samples are also consistent with the above model of nanographite-chlorine interaction.
机译:介绍了在其与吸附氯分子相互作用期间发生的多层石墨烯纳米蛋白(纳米岩纳米蛋白(纳米岩)的电子结构和磁性性能的研究结果。在FERMI能量E_F处的电流载体D(E_F)的状态密度的发现可逆降低可以通过纳米型纳米簇的旋转分裂来解释由于增加而引起的电子 - 电子相互作用的增加D(E_F)在从纳米凝块到氯adaToms的电子密度部分转移。局部旋转浓度的揭示不可逆转的减少表明,边缘碳原子的氯和未配对(侧冗余)的电子旋转也在该相互作用上偶联,即纳米载体的边缘共价化合物具有氯形式。根据吸附氯分子的量和氯化样品中的温度的π电子的变化的性质也与上述纳米氯相互作用的模型一致。

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