Abstract: In this work, we propose an electrical strategy to extract further more information on an electrolyte cation's nature than its concentration, out of a single organic electrochemical transistor (OECT): a biocompatible device which is nowadays attracting v ery much attention as a sensor platform for bioelectronics. Based on an optimized OECT structure,the systematic study by impedance spectroscopy of 6 different chloride salts over 12 different concentrations demonstrated that the impedance of the OECT dev ice is governed either by electrical or electrolytic transport mechanisms, depending on the frequency range of the study. From both of these ion-dependent impedances, on can extract either the conductance of the electrolytes or the one of the dedoped pol y(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS). From the boundaries of both of these very different ion-limited mechanisms, we extracted two uncorrelated ion-dependent output, accessing to information on the electrolyte cation's nature apart from its concentration. This strategy can be implemented in dynamic analysis of complex ionic media, such as for cellular-activity sensing, in order to discriminate cationic flows, without introducing any foreign ion-selective material, which can t hreaten the biocompatibility.
Pecqueur S., Lenfant S., Guérin D., Alibart F., Vuillaume D.
Abstract: The invention relates to an organic electronic component (100) comprising at least one charge generation layer (5) which has an organically p-doped region (5a) that contains a zinc complex as a p-dopant, said zinc complex in turn containing at least one ligand L of the following structure: formula (I) wherein R1 and R2 can be oxygen, sulphur, selenium, NH or NR4 independently from one another, wherein R4 is selected from the group containing alkyl or aryl and which can be bonded to R3; and wherein R3 is selected from the group containing alkyl, long-chain alkyl, cycloalkyl, halogen alkyl, at least partially halogenated long-chain alkyl, halogen cycloalkyl, aryl, arylene, halogen aryl, heteroaryl, heteroarylene, heterocyclic alkylene, heterocycloalkyl, halogen heteroaryl, alkenyl, halogen alkenyl, alkynyl, halogen alkynyl, ketoaryl, halogen ketoaryl, ketoheteroaryl, ketoalkyl, halogen ketoalkyl, ketoalkenyl, halogen ketoalkenyl, halogen alkyl aryl, and halogen alkyl heteroaryl, wherein, for suitable gr oups, one or a number of non-adjacent CH2 groups can be replaced by -O-, -S-, -NH-, -NR°°°-, -SiR°R°°-, -CO-, -COO-, -COR°OR°°-, -OCO-, -OCO-O-, -SO2-, -S-CO-, -CO-S-, -O-CS-, -CS-O-, -CY1=CY2 or -C≡C- independently from one another, and in such a way that O and/or S atoms are not directly bonded to one another, and are replaced optionally with aryl- or heteroaryl preferably containing between 1 and 30 C atoms (terminal CH3 groups are understood to be CH2 groups in the sense of CH2-H). The invention further relates to the use of a zinc complex as a p-dopant in charge generation layers.
Kessler F., Maltenberger A., Pecqueur S., Pentlehner D., Regensburger S., Schmid G.
Abstract: We report on hydrazine-sensing organic electrochemical transistors (OECTs) with a design consisting of concentric annular electrodes. The design engineering of these OECTs was motivated by the great potential of using OECT sensing arrays in fields such a s bioelectronics. In this work, poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)-based OECTs have been studied as aqueous sensors that are specifically sensitive to the lethal hydrazine molecule. These amperometric sensors have many re levant features for the development of hydrazine sensors, such as a sensitivity down to 10-5 M of hydrazine in water, an order of magnitude higher selectivity for hydrazine than for nine other water-soluble common analytes, the capability to e ntirely recover its base signal after water flushing, and a very low operation voltage. The specificity for hydrazine to be sensed by our OECTs is caused by its catalytic oxidation at the gate electrode, and enables an increase in the output current modu lation of the devices. This has permitted the device-geometry study of the whole series of 80 micrometric OECT devices with sub-20-nm PEDOT:PSS layers, channel lengths down to 1 μm, and a specific device geometry of coplanar and concentric electrodes . The numerous geometries unravel new aspects of the OECT mechanisms governing the electrochemical sensing behaviours of the device - more particularly the effect of the contacts which are inherent at the micro-scale. By lowering the device cross-talk, m icrometric gate-integrated radial OECTs shall contribute to the diminishing of the readout invasiveness and therefore further promote the development of OECT biosensors.
Pecqueur S.*, Lenfant S., Guérin D., Alibart F., Vuillaume D.
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