Work Function Variations in Twisted Graphene Layers

• Published in: Scientific reports Vol. 8; no. 1; pp. 2006 - 9
• Main Authors: Robinson, Jeremy T., Culbertson, James, Berg, Morgann, Ohta, Taisuke
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 31-01-2018; Nature Publishing Group
• Subjects: 140/133; 639/301/357/918; 639/301/357/918/1052; 639/301/357/918/1053; Electron microscopy; Humanities and Social Sciences; MATERIALS SCIENCE; Microscopy; multidisciplinary; Raman spectroscopy; Science; Science (multidisciplinary)
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-19631-4

By combining optical imaging, Raman spectroscopy, kelvin probe force microscopy (KFPM), and photoemission electron microscopy (PEEM), we show that graphene’s layer orientation, as well as layer thickness, measurably changes the surface potential (Φ). Detailed mapping of variable-thickness, rotationally-faulted graphene films allows us to correlate Φ with specific morphological features. Using KPFM and PEEM we measure ΔΦ up to 39 mV for layers with different twist angles, while ΔΦ ranges from 36–129 mV for different layer thicknesses. The surface potential between different twist angles or layer thicknesses is measured at the KPFM instrument resolution of ≤ 200 nm. The PEEM measured work function of 4.4 eV for graphene is consistent with doping levels on the order of 10
12
cm
−2
. We find that Φ scales linearly with Raman G-peak wavenumber shift (slope = 22.2 mV/cm
−1
) for all layers and twist angles, which is consistent with doping-dependent changes to graphene’s Fermi energy in the ‘high’ doping limit. Our results here emphasize that layer orientation is equally important as layer thickness when designing multilayer two-dimensional systems where surface potential is considered.