Add like
Add dislike
Add to saved papers

Bias induced ferromagnetism and half-metallicity in graphene nano-ribbons.

Scientific Reports 2017 December 7
Towards spin selective electronics made of three coordinated carbon atoms, here we computationally propose robust and reversibly bias driven evolution of pristine undoped graphene nano-ribbons(GNR) into ferromagnetic-semiconductor, metal or a half metal, irrespective of their edge configurations. The evolution is a result of a rare ferromagnetic(FM) order emerging among nearest neighbouring(n-n) sites, in positively biased regions in their in-homogeneous bias unit-cells, in attempt to cooperatively minimise on-site Coulomb repulsion and kinetic energy, while maximising localization of electrons at the positively biased sites. The phenomenon appears to be a general property of in-homogeneously biased Coulomb correlated bipartite systems. Consequences are particularly rich in zigzag edged graphene nano-ribbons(ZGNR) due to the contest of bias driven n-n FM order and the inter-edge antiferromagnetic order inherent to ZGNRs, leading to systematic closing of gap for one of the spins, amounting to bias controlled unmissable opening of window for FM-semiconducting and half-metallic transport.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app