Abstract

The surface diffusion (dissipation) of charge carriers enhanced by water molecules in solution-based biosensors and ambient operating gas sensors strongly influence their resistance response, sensitivity, and stability in time. Therefore, the information on the charge distribution at interfaces of conductive and insulating parts is essential for the operating sensors. This work presents the simultaneous measurement of the longitudinal macroscopic resistance response and local surface potential (SP) mapping by Kelvin probe force microscopy (KPFM) on a graphene Hall bar sensor. The results show the propagation of an electric charge from the main graphene channel onto the neighboring SiO2 surface. The charge propagation strongly increases with the relative humidity and can be controlled by a bottom-gate voltage used in most sensors based on a field effect transistor (FET) architecture. As proved by the longitudinal resistance measurements, the resulting side charge accumulation has a very small impact on the 2D resistivity of the graphene channel. It has been explained by an application of the Thomas-Fermi theory, proving an efficient screening of side accumulated charge potential caused by a redistribution of the charge inside the wide graphene channel. The combination of a transport resistance response and KPFM provides a deeper understanding of sensors/biosensors functionality and their design features than a simple resistance response usually observed.

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