Direct Visualization of the Charge Transfer in a Graphene/α-RuCl3 Heterostructure via Angle-Resolved Photoemission Spectroscopy

  • Antonio Rossi
  • , Cameron Johnson
  • , Jesse Balgley
  • , John C. Thomas
  • , Luca Francaviglia
  • , Riccardo Dettori
  • , Andreas K. Schmid
  • , Kenji Watanabe
  • , Takashi Taniguchi
  • , Matthew Cothrine
  • , David G. Mandrus
  • , Chris Jozwiak
  • , Aaron Bostwick
  • , Erik A. Henriksen
  • , Alexander Weber-Bargioni
  • , Eli Rotenberg

Research output: Contribution to journalArticlepeer-review

Abstract

We investigate the electronic properties of a graphene and α-ruthenium trichloride (α-RuCl3) heterostructure using a combination of experimental techniques. α-RuCl3 is a Mott insulator and a Kitaev material. Its combination with graphene has gained increasing attention due to its potential applicability in novel optoelectronic devices. By using a combination of spatially resolved photoemission spectroscopy and low-energy electron microscopy, we are able to provide a direct visualization of the massive charge transfer from graphene to α-RuCl3, which can modify the electronic properties of both materials, leading to novel electronic phenomena at their interface. A measurement of the spatially resolved work function allows for a direct estimate of the interface dipole between graphene and α-RuCl3. Their strong coupling could lead to new ways of manipulating electronic properties of a two-dimensional heterojunction. Understanding the electronic properties of this structure is pivotal for designing next generation low-power optoelectronics devices.

Original languageEnglish
Pages (from-to)8000-8005
Number of pages6
JournalNano Letters
Volume23
Issue number17
DOIs
StatePublished - Sep 13 2023

Keywords

  • Graphene
  • a-RuCl
  • angle-resolved photoemission spectroscopy
  • electronic structure
  • low energy electron microscopy
  • p−n junction

Fingerprint

Dive into the research topics of 'Direct Visualization of the Charge Transfer in a Graphene/α-RuCl3 Heterostructure via Angle-Resolved Photoemission Spectroscopy'. Together they form a unique fingerprint.

Cite this