H. Hahn

A nanoparticulate indium tin oxide field-effect transistor with solid electrolyte gating

Reversible tuning of the transport properties of metallic conducting systems is not reported widely in the literature. Here, we report a junction field-effect transistor (FET) based on a transparent conducting oxide (TCO) nanoparticle channel and a solid polymer electrolyte as a gate. The device principle is based on the variation of the drain current induced by the capacitive double layer charging at the electrolyte/nanoparticle interfaces. A device with a metallic conducting channel made of indium tin oxide (ITO) nanoparticles exhibits an on/off ratio of 2 × 10(3) even when the gate potential is limited within the electrochemical capacitive region to avoid redox reactions at the interface. An FET device with metal-like conductance is always favored for the low dimensions of the device and a high on-state current. The field-effect mobility is calculated to be 24.3xa0cm(2)xa0V(-1)xa0s(-1). A subthreshold swing between 230 and 425xa0mVxa0dec(-1) is observed.

Electric field induced reversible tuning of resistance of thin gold films

The change in resistance of nanostructured metals with respect to an applied field is believed to be due to a change in carrier concentration and hence a linear variation of resistance with the surface charge is expected. In this article, we propose a different approach to explain the resistance variation based on a change in the effective thickness of the film due to a shift of the electron density profile resulting from the applied surface charge. The change in effective thickness together with its effect on surface scattering of electrons account for the majority of the observed variation in resistance. The thin film geometry with different thicknesses and hence a controlled variation of the surface-to-volume ratio allows a deep quantitative understanding and interpretation of the observed phenomena. The model presented in this work shows that a nominal nonlinear response of the resistance of a metal on electrochemically applied surface charge does not necessarily indicate an onset of a redox reaction.