Issue 43, 2016

Electron-doping induced half-metallicity in one-dimensional Co-dithiolene molecular wires

Abstract

Motivated by experimental synthesis of a unique one dimensional organometallic Co-dithiolene molecular wire, we employ density functional calculations to study its electronic and magnetic properties. The ground state of this molecular wire is identified to be an antiferromagnetic (AFM) semiconductor with a medium-sized indirect band gap. However, it could be converted into an intriguing ferromagnetic (FM) half-metal via electron doping. The spontaneous occurrence of ferromagnetism is driven by the enhanced density of states at the Fermi level when sufficient electrons are doped, which can be well understood from the Stoner model. Our results would open new possibilities for applying the Co-dithiolene molecular wire in spin-based electronic devices besides its efficient applications in hydrogen evolution reactions.

Graphical abstract: Electron-doping induced half-metallicity in one-dimensional Co-dithiolene molecular wires

Supplementary files

Article information

Article type
Paper
Submitted
02 Там. 2016
Accepted
15 Қыр. 2016
First published
16 Қыр. 2016

J. Mater. Chem. C, 2016,4, 10209-10214

Electron-doping induced half-metallicity in one-dimensional Co-dithiolene molecular wires

T. Zhang, L. Zhu and G. Chen, J. Mater. Chem. C, 2016, 4, 10209 DOI: 10.1039/C6TC03297D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements