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单分子磁体单层的穆斯堡尔光谱学。

Mössbauer spectroscopy of a monolayer of single molecule magnets.

作者信息

Cini Alberto, Mannini Matteo, Totti Federico, Fittipaldi Maria, Spina Gabriele, Chumakov Aleksandr, Rüffer Rudolf, Cornia Andrea, Sessoli Roberta

机构信息

Department of Physics and Astronomy and INSTM Research Unit, University of Florence, 50019, Sesto Fiorentino, Italy.

Department of Chemistry 'Ugo Schiff' and INSTM Research Unit, University of Florence, 50019, Sesto Fiorentino, Italy.

出版信息

Nat Commun. 2018 Feb 2;9(1):480. doi: 10.1038/s41467-018-02840-w.

Abstract

The use of single molecule magnets (SMMs) as cornerstone elements in spintronics and quantum computing applications demands that magnetic bistability is retained when molecules are interfaced with solid conducting surfaces. Here, we employ synchrotron Mössbauer spectroscopy to investigate a monolayer of a tetrairon(III) (Fe) SMM chemically grafted on a gold substrate. At low temperature and zero magnetic field, we observe the magnetic pattern of the Fe molecule, indicating slow spin fluctuations compared to the Mössbauer timescale. Significant structural deformations of the magnetic core, induced by the interaction with the substrate, as predicted by ab initio molecular dynamics, are also observed. However, the effects of the modifications occurring at the individual iron sites partially compensate each other, so that slow magnetic relaxation is retained on the surface. Interestingly, these deformations escaped detection by conventional synchrotron-based techniques, like X-ray magnetic circular dichroism, thus highlighting the power of synchrotron Mössbauer spectroscopy for the investigation of hybrid interfaces.

摘要

将单分子磁体(SMM)用作自旋电子学和量子计算应用中的基石元素,要求分子与固体导电表面接触时保持磁双稳态。在此,我们利用同步辐射穆斯堡尔谱研究化学接枝在金基底上的单层四铁(III)(Fe)单分子磁体。在低温和零磁场下,我们观察到Fe分子的磁模式,表明与穆斯堡尔时间尺度相比自旋涨落缓慢。如从头算分子动力学所预测的,还观察到与基底相互作用引起的磁核显著结构变形。然而,各个铁位点发生的修饰效应部分相互补偿,因此表面上仍保留缓慢的磁弛豫。有趣的是,这些变形通过基于同步辐射的传统技术(如X射线磁圆二色性)未被检测到,从而突出了同步辐射穆斯堡尔谱在研究混合界面方面的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d83/5797240/56d9bfb8022a/41467_2018_2840_Fig1_HTML.jpg

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