Shantanu Mishra^1*, Doreen Beyer², Kristjan Eimre¹, Ricardo Ortiz^3,4, Joaquín Fernández‐Rossier⁵, Reinhard Berger², Oliver Gröning¹, Carlo A. Pignedoli^1*, Roman Fasel^1,6, Xinliang Feng², Pascal Ruffieux^1*

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

2 Center for Advancing Electronics and Department of Chemistry and Food Chemistry, Technical University of Dresden, 01062 Dresden, Germany

3 Department of Applied Physics, University of Alicante, 03690 Sant Vicent del Raspeig, Spain

4 Department of Chemical Physics, University of Alicante, 03690 Sant Vicent del Raspeig, Spain

5 QuantaLab, International Iberian Nanotechnology Laboratory, 4715-330 Braga, Portugal

6 Department of Chemistry and Biochemistry, University of Bern, 3012 Bern, Switzerland

* Corresponding authors emails: shantanu.mishra@empa.ch, carlo.pignedoli@empa.ch, pascal.ruffieux@empa.ch

DOI10.24435/materialscloud:5k-rm [version v1]

Publication date: Oct 14, 2020

How to cite this record

Shantanu Mishra, Doreen Beyer, Kristjan Eimre, Ricardo Ortiz, Joaquín Fernández‐Rossier, Reinhard Berger, Oliver Gröning, Carlo A. Pignedoli, Roman Fasel, Xinliang Feng, Pascal Ruffieux, Collective all‐carbon magnetism in triangulene dimers, Materials Cloud Archive 2020.122 (2020), https://doi.org/10.24435/materialscloud:5k-rm

Description

This record contain data to support the result we published in the work "Collective All‐Carbon Magnetism in Triangulene Dimers". Triangular zigzag nanographenes, such as triangulene and its π‐extended homologues, have received widespread attention as organic nanomagnets for molecular spintronics, and may serve as building blocks for high‐spin networks with long‐range magnetic order, which are of immense fundamental and technological relevance. In the publication we present the on‐surface synthesis and a proof‐of‐principle experimental study of magnetism in covalently bonded triangulene dimers. On‐surface reactions of rationally designed precursor molecules on Au(111) lead to the selective formation of triangulene dimers in which the triangulene units are either directly connected through their minority sublattice atoms, or are separated via a 1,4‐phenylene spacer.

Materials Cloud sections using this data

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ReadMe.yaml MD5md5:7a8f2c2c422bf6938d62020a65c52a5e	19.4 KiB	ReadMe file in yaml format listing all files contained in the record
data.tgz MD5md5:9d50b07ce32a87dd0a11c3a2c31be291	27.2 MiB	Tar archive containing all files of the record
dft_calculations.aiida MD5md5:c04da8e117a662419055c68e338da9d9 Open this AiiDA archive on renkulab.io (https://renkulab.io/)	146.9 MiB	Input and output files for DFT calculations performed for this work. The file is an archive of AiiDA nodes

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External references

Keywords

nanographenes magnetic carbon spin chains MARVEL/DD3 SNSF ERC