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铁磁耦合自旋-1纳米石墨烯中的磁激发

Magnetic Excitations in Ferromagnetically Coupled Spin-1 Nanographenes.

作者信息

Turco Elia, Wu Fupeng, Catarina Gonçalo, Krane Nils, Ma Ji, Fasel Roman, Feng Xinliang, Ruffieux Pascal

机构信息

Empa - Swiss Federal Laboratories for Materials Science and Technology nanotech@surfaces Laboratory, 8600, Dübendorf, Switzerland.

Max Planck Institute of Microstructure Physics Weinberg 2, 06120 Halle, Germany.

出版信息

Angew Chem Int Ed Engl. 2024 Dec 20;63(52):e202412353. doi: 10.1002/anie.202412353. Epub 2024 Nov 6.

Abstract

In the pursuit of high-spin building blocks for the formation of covalently bonded 1D or 2D materials with controlled magnetic interactions, -electron magnetism offers an ideal framework to engineer ferromagnetic interactions between nanographenes. As a first step in this direction, we explore the spin properties of ferromagnetically coupled triangulenes-triangular nanographenes with spin . By combining in-solution synthesis of rationally designed molecular precursors with on-surface synthesis, we successfully achieve covalently bonded triangulene dimers and trimers on Au(111). Starting with the triangulene dimer, we meticulously characterize its low-energy magnetic excitations using inelastic electron tunneling spectroscopy (IETS). IETS reveals conductance steps corresponding to a quintet-to-triplet excitation, and a zero-bias peak resulting from higher-order spin-spin scattering of the five-fold degenerate ferromagnetic ground state. The Heisenberg model captures the key parameters of inter-triangulene ferromagnetic exchange, and its successful extension to the larger system validates the model's accuracy. We anticipate that incorporating ferromagnetically coupled building blocks into the repertoire of magnetic nanographenes will unlock new possibilities for designing carbon nanomaterials with complex magnetic ground states.

摘要

在追求用于形成具有可控磁相互作用的共价键合一维或二维材料的高自旋构建块的过程中,π电子磁性为设计纳米石墨烯之间的铁磁相互作用提供了一个理想的框架。作为朝着这个方向迈出的第一步,我们探索了具有自旋1/2的铁磁耦合三角烯——三角形纳米石墨烯的自旋特性。通过将合理设计的分子前体的溶液内合成与表面合成相结合,我们成功地在Au(111)上实现了共价键合的三角烯二聚体和三聚体。从三角烯二聚体开始,我们使用非弹性电子隧穿光谱(IETS)精心表征其低能磁激发。IETS揭示了对应于五重态到三重态激发的电导台阶,以及由五重简并铁磁基态的高阶自旋-自旋散射产生的零偏置峰。海森堡模型捕捉了三角烯间铁磁交换的关键参数,并且它成功扩展到更大的三聚体系统验证了该模型的准确性。我们预计将铁磁耦合构建块纳入磁性纳米石墨烯的体系中将为设计具有复杂磁基态的碳纳米材料开辟新的可能性。

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