Journal
JOURNAL OF ALLOYS AND COMPOUNDS
Volume 940, Issue -, Pages -Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2022.168693
Keywords
Graphdiyne; Kagome lattice; Room temperature ferromagnetic
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In this paper, cobalt-doped graphdiyne nanosheets were successfully synthesized by introducing transition metal cobalt into the alkynyl unit of graphdiyne using a bottom-up liquid-liquid interface synthesis method. The obtained nanosheets showed obvious room temperature ferromagnetism. Density function theory results indicated that cobalt-doped graphdiyne is a half-metallic material with a kagome lattice, and the embedded cobalt atoms are the source of magnetic moment. The special kagome structure exhibited flat band ferromagnetism, consistent with the experimental observations. The successful synthesis of cobalt-doped graphdiyne not only promotes the study of graphdiyne's magnetism, but also provides a new route for the experimental synthesis of kagome lattice materials.
Graphdiyne, being considered as a new potential spintronics material, possesses excellent electronic and magnetic properties. However, how to introduce ferromagnetic order into graphdiyne is still a pending issue not yet solved, which limits its further application. In this paper, transition metal cobalt is introduced into the alkynyl unit of graphdiyne by a bottom-up liquid-liquid interface synthesis method and the ob-tained cobalt-doped graphdiyne nanosheets are found to exhibit obvious room temperature ferro-magnetism. The density function theory results show that cobalt-doped graphdiyne is half-metallic with a kagome lattice and the imbedded cobalt atoms are the source of magnetic moment. The special kagome structure presents flat band ferromagnetism, which consists with the magnetism behaviour observed in experiment. The successful synthesis of cobalt-doped graphdiyne can not only promote the magnetic in-vestigation of graphdiyne, but provide a new route for the experimental synthesis of kagome lattice ma-terials as well.(c) 2023 Elsevier B.V. All rights reserved.
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