Liquid electrolyte positioning along the device channel influences the operation of Organic Electro-Chemical Transistors
Gentile, Francesco T.
Di Fabrizio, Enzo M.
KAUST DepartmentMaterial Science and Engineering Program
Physical Science and Engineering (PSE) Division
Permanent link to this recordhttp://hdl.handle.net/10754/563819
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AbstractIn this work, we show the influence of the liquid electrolyte adsorption by porous films made of poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate), PEDOT:PSS, on the operation of an Organic Electro-Chemical Transistor with an active channel based on these polymeric films. In particular, the effect of film hydration on device performance is evaluated by studying its electrical response as a function of the spatial position between the electrolyte and the channel electrodes. This is done by depositing a PEDOT:PSS film on a super-hydrophobic surface aimed at controlling the electrolyte confinement next to the electrodes. The device response shows that the confinement of ionic liquids near to the drain electrode results in a worsening of the current modulation. This result has been interpreted in the light of studies dealing with the transport of ions in semiconducting polymers, indicating that the electrolyte adsorption by the polymeric film implies the formation of liquid pathways inside its bulk. These pathways, in particular, affect the device response because they are able to assist the drift of ionic species in the electrolyte towards the drain electrode. The effect of electrolyte adsorption on the device operation is confirmed by means of moving-front measurements, and is related to the reproducibility of the device operation curves by measuring repeatedly its electrical response.
CitationD’ Angelo, P., Coppedè, N., Tarabella, G., Romeo, A., Gentile, F., Iannotta, S., … Mosca, R. (2014). Liquid electrolyte positioning along the device channel influences the operation of Organic Electro-Chemical Transistors. Organic Electronics, 15(11), 3016–3023. doi:10.1016/j.orgel.2014.08.029
SponsorsThis work has been supported by the Project BioNiMed (Multifunctional Hybrid Nanosystems for Biomedical Applications) from Fondazione Cassa di Risparmio di Parma (CARIPARMA) and by the N-Chem project within the CNR-NANOMAX Flagship program.