Issue 30, 2025

Strong magnetic exchange coupling of a dibenzo-fused rhomboidal nanographene and its homocoupling with tunable periodicities on a metal surface

Abstract

Open-shell nanographenes (NGs), also known as molecular π-magnets, have recently garnered attention for their potential in spintronics and quantum computing. Tailoring of such NGs at the atomic level allows the control of their magnetic interactions. We report here the on-surface synthesis of a dibenzo-fused rhomboidal NG with predominant zigzag edges featuring an open-shell (antiferromagnetic) character and a high value of magnetic exchange coupling (MEC) on Au(111) surfaces. Scanning tunneling microscopy (STM) and noncontact atomic force microscopy (nc-AFM) confirm its chemical structure. Scanning tunneling spectroscopy (STS) measurements, complemented by state-of-the-art theoretical calculations, reveal the open-shell character of the NG, observed as singlet−triplet inelastic excitations. Furthermore, molecular chains consisting of these NGs were fabricated with tunable periodicities through the functionalization of the precursor, showing the absence of MEC between adjacent units, which provides deeper insights into the behavior of open-shell systems and preservation of individual magnetic entities within π-conjugated structures.

Graphical abstract: Strong magnetic exchange coupling of a dibenzo-fused rhomboidal nanographene and its homocoupling with tunable periodicities on a metal surface

Supplementary files

Article information

Article type
Paper
Submitted
04 Mar 2025
Accepted
02 Jul 2025
First published
17 Jul 2025
This article is Open Access
Creative Commons BY-NC license

Nanoscale, 2025,17, 17769-17776

Strong magnetic exchange coupling of a dibenzo-fused rhomboidal nanographene and its homocoupling with tunable periodicities on a metal surface

A. Barragán, Goudappagouda, M. Kumar, D. Soler-Polo, E. Pérez-Elvira, A. Pinar Solé, A. García-Frutos, Z. Gao, K. Lauwaet, J. M. Gallego, R. Miranda, D. Écija, P. Jelínek, A. Narita and J. I. Urgel, Nanoscale, 2025, 17, 17769 DOI: 10.1039/D5NR00957J

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