Magnetic exchange interaction between unpaired π- and d-electrons in nanographene-metal coordination complexes

The combination of open-shell nanographenes (NGs) and magnetic transition metals holds great promise for generating various new quantum phases applicable in spintronics and quantum information technologies. However, a crucial aspect in accomplishing this is to comprehend the magnetic exchange interactions between unpaired π- and d-electrons, a topic that has been seldom addressed. In this study, we focus on magnetic π-d exchange interactions between open-shell NGs and a magnetic coordination center of Fe or Co by employing scanning tunneling microscopy and spectroscopy. We synthesize two sets of NG-metal coordination complexes on a Au(111) substrate, secured by coordination bonds of carboxyl acid-Fe (Co). Through analysis of the excitation spectra, we observe a characteristic exchange coupling of 9 meV (5 meV) between the unpaired π-electron and the Fe (Co) d-shell electrons. Our experimental findings are qualitatively in agreement with multiconfigurational quantum chemistry calculations. This work provides evidence that a substantial magnetic exchange coupling can be achieved and engineered in metal-organic coordination systems, paving the way for designing and customizing extended radical metal-organic frameworks with precisely tailored magnetic properties.

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Publication Details

Journal
National Science Review
Published
2025-01-27
DOI
https://doi.org/10.1093/nsr/nwaf033
Citations
6
Primary Topic
Magnetism in coordination complexes
Type
article
Field-Weighted Citation Impact
2.56

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article

Magnetic exchange interaction between unpaired π- and d-electrons in nanographene-metal coordination complexes

Jinfeng Jia, Dandan Guan, Thomas Frederiksen, Yaoyi Li et al.
6 citations
National Science Review
Magnetism in coordination complexes
2.56
article

Magnetic exchange interaction between unpaired π- and d-electrons in nanographene-metal coordination complexes

Jinfeng Jia, Dandan Guan, Thomas Frederiksen, Yaoyi Li, Canhua Liu, Yashi Jiang, Pei Nian Liu, Hao Zheng, Deng‐Yuan Li, Bingkai Yuan, Liang Liu, Can Li, Xiaoxue Liu, Shiyong Wang, Bingxin Wang, Ricardo Ortiz, Xin-Yu Zhang, Yuqiang Zheng
article en
6 citations

Abstract

The combination of open-shell nanographenes (NGs) and magnetic transition metals holds great promise for generating various new quantum phases applicable in spintronics and quantum information technologies. However, a crucial aspect in accomplishing this is to comprehend the magnetic exchange interactions between unpaired π- and d-electrons, a topic that has been seldom addressed. In this study, we focus on magnetic π-d exchange interactions between open-shell NGs and a magnetic coordination center of Fe or Co by employing scanning tunneling microscopy and spectroscopy. We synthesize two sets of NG-metal coordination complexes on a Au(111) substrate, secured by coordination bonds of carboxyl acid-Fe (Co). Through analysis of the excitation spectra, we observe a characteristic exchange coupling of 9 meV (5 meV) between the unpaired π-electron and the Fe (Co) d-shell electrons. Our experimental findings are qualitatively in agreement with multiconfigurational quantum chemistry calculations. This work provides evidence that a substantial magnetic exchange coupling can be achieved and engineered in metal-organic coordination systems, paving the way for designing and customizing extended radical metal-organic frameworks with precisely tailored magnetic properties.

National Science ReviewVol. 12(4)
Ikerbasque (ES), East China University of Science and Technology (CN), China Pharmaceutical University (CN), Shanghai Jiao Tong University (CN), Chinese Academy of Sciences (CN), Hefei University (CN), Suzhou Institute of Nano-tech and Nano-bionics (CN), State Key Laboratory of Chemical Engineering (CN), Donostia International Physics Center (ES)
European Commission, National Natural Science Foundation of China, Chinese Academy of Sciences, Science and Technology Commission of Shanghai Municipality, Agencia Estatal de Investigación
Openalex Percentile: Top 11%
Magnetism in coordination complexes
2.56
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