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On-surface structural and electronic properties of spontaneously formed Tb2Pc3 single molecule magnets

机译:表面结构和电子性质自发形成Tb2Pc3单分子磁铁

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摘要

The single molecule magnet (SMM) bis(phthalocyaninato)terbium(iii) (TbPc2) has received significant and increasing attention as an exemplar system for realizing molecule-based spin electronics. Attaining higher nuclearity via multi-decker TbPc systems has remained an outstanding challenge, as known examples of Tb2Pc3 systems are only those containing Pc rings with substituents (e.g. alkyl, alkoxyl). Here we report on the spontaneous formation of Tb2Pc3 species from TbPc2 precursors via sublimation in ultrahigh vacuum (UHV) onto an Ag(111) surface. The presence of Tb2Pc3 molecules on the surface are inspected using scanning probe microscopy with submolecular resolution supported by density functional theory (DFT) calculations and additional chemical analysis. We observe the selective presence of a Kondo resonance (30 K) in the Tb2Pc3 species, that we attribute to differences in the orientation of the internal molecular ligands. Formation of triple-decker complexes offers new possibilities to study and control magnetic interactions not accessible with standard TbPc2 molecules.
机译:单分子磁体(多发性骨髓瘤)bis (phthalocyaninato)铽(iii) (TbPc2)收到了显著的和越来越多的关注基于一个范例系统实现分子自旋电子学。一直保持一个多层TbPc系统杰出的挑战,众所周知的例子Tb2Pc3系统只有那些包含电脑响了与取代基(如烷基、烷氧基的)。报告Tb2Pc3自发形成的物种从TbPc2前体通过升华超高真空(特高压)到一个Ag(111)表面。Tb2Pc3分子在表面的存在使用扫描探针显微镜检查吗submolecular分辨率支持的密度泛函理论(DFT)计算额外的化学分析。选择性的近藤共振(30 K)Tb2Pc3物种,我们属性内部的方向的差异分子配体。复合物研究提供了新的可能性控制磁相互作用无法访问标准TbPc2分子。

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