A well-established technology to produce high quality graphene is by heating up silicon carbide (SiC) in the presence of inert Argon gas. Under proper growth conditions, this technique results in so-called epitaxial single layer graphene on the surface of silicon carbide (epigraphene). Compared to graphene grown by other methods, epigraphene grows as a single crystal over the entire silicon carbide substrate, anticipating higher electronic quality with respect to polycrystalline graphene grown by other methods. However, on SiC, the graphene layer interacts very strongly with the substrate resulting in very large transfer of electrons from SiC into the graphene layer. To fully explore and exploit the properties of graphene requires the capability to tune the amount of electrons transferred from the substrate. For epigraphene, the very strong interaction between the graphene layer and SiC substrate makes is difficult control at will the amount of electron transfer (i.e. doping). The inability to finely dope epigraphene has been a major challenge in studying and exploiting the properties of this promising material.
The scientists have discovered a novel method to carefully assemble molecules on the surface of epigraphene to dope it with unprecedentedly high control, while keeping intact its electronic quality. The method utilizes polymers to assist the assembly of electron-accepting molecules (i.e. dopants) on the surface of graphene; once in contact with graphene, dopant molecules withdraw electron from graphene and this interaction keeps molecule in place. To achieve this, polymers are mixed with dopant molecules, and this blend is then deposited on the epigraphene substrate by simple spin-coating, which is a standard and scalable microfabrication step performed in ambient conditions.
“By carefully choosing the polymer, the molecular dopant and the substrate, we have obtained rather exciting results. With a simple spin-coating step, which is routine work in cleanroom environment, we can heal epitaxial graphene and produce a centimeter-scale Dirac material with very high electronic quality. The electronic disorder that we measure in the resulting doped graphene is lower than that of microscopic graphene flakes encapsulated by hexagonal Boron Nitride (hBN), which is the method that thus far results in the highest quality graphene”, says Samuel Lara-Avila (above picture), Assistant Professor at the Quantum Device Physics Laboratory at the Department of Microtechnology and Nanoscience – MC2, at Chalmers.
“This is a very unusual example of a highly uniform system that arises from the combination of “dirty” elements: epitaxial graphene is regarded as a lower quality material compared to exfoliated graphene flakes, and both dopants and polymers are known to deteriorate the electronic qualities of graphene. But the combination yields high mobility epigraphene, doped to the Dirac point with high uniformity over macroscopic scale”, adds Sergey Kubatkin (to the right), Professor in the same lab.
The researchers used a combination of the common polymer poly methyl methacrylate (PMMA) and the well-known F4TCNQ acceptor molecule to form the dopant blend. They discovered that when the dopant blend is deposited on epigraphene, molecular dopants (i.e. F4TCNQ) diffuse through the polymer and spontaneously assemble at the epigraphene-polymer interface, making a densely packed layer of 3-4 molecules per square nanometer. Surprisingly, this dense assembly of molecules results in epigraphene doped close to the Dirac point with an exceptionally small amount of charge inhomogeneity, i.e. disorder.
Using epigraphene, these results simultaneously show the potency of this method, because epitaxial graphene grown on SiC is particularly difficult to dope while at the same time maintaining its electronic quality.
“We have made a significant progress in approaching a largely unexplored realm of graphene research – a study of delicate fascinating physical properties of macroscopic graphene samples doped at the Dirac point, in which electron transport measurements are not obscured by size-induced mesoscopic effects and charge puddles, typical of microscopic samples”, says Hans He (to the right), PhD student in the group.
This method can be the key to explore and exploit the fascinating physical properties of epigraphene and other related Dirac materials. While there exist world-wide efforts to synthesize high quality materials, unintentional impurities or hard-to-reach stoichiometry during material growth result in heavily doped crystals. In this situation, at high doping levels, the interesting physics of Dirac materials might be obscured or entirely absent. A few other examples of novel physical effects expected – made possible by the new results – include study of metal-insulator transitions, interacting Dirac fermions, Wigner crystallization, possibility to observe Zitterbewegung of electrons in Dirac materials, and specular Andreev reflections among others.
“The resulting doped epigraphene is also of technological relevance, and the material is readily applicable in quantum resistance metrology, light sensors and magnetic sensors. But the molecular assembly method can open other research avenues by using a different combination of polymer/dopants, and also when applied to other atomically thin materials”, concludes Samuel Lara- Avila.
The research, at the border between polymer chemistry and solid state physics, was a collaborative effort between groups at the Department of Microtechnology and Nanoscience – MC2 – and the Department of Chemistry and Chemistry Engineering at Chalmers. It was jointly supported by the Swedish Foundation for Strategic Research (SSF), Knut and Alice Wallenberg Foundation, Chalmers Excellence Initiative Nano, the Swedish Research Council (VR), the Swedish-Korean Basic Research Cooperative Program of the NRF, and European Union’s Horizon 2020 research and innovation program.
Photo of Samuel Lara-Avila: Jan-Olof Yxell
Photos of Sergey Kubatkin and Hans He: Michael Nystås
Read the article in Nature Communications >>>
1. H. He, K. H. Kim, A. Danilov, D. Montemurro, L. Yu, Y. W. Park, F. Lombardi, T. Bauch, K. Moth-Poulsen, T. Iakimov, R. Yakimova, P. Malmberg, C. Müller, S. Kubatkin, S. Lara-Avila, Uniform doping of graphene close to the charge neutrality point by polymer-assisted spontaneous assembly of molecular dopants. Nat. Commun. 9, 3956 (2018).