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Comprehensive Summary: The analytical performance of H+‐selective solid‐contact ion‐selective electrodes (SCISEs) based on solid contact polyaniline doped with chloride (PANI(Cl)) and poly(3,4‐ethylenedioxythiophene) doped with poly(styrene sulfonate) (PEDOT(PSS)) was characterized by a developed coulometric signal transduction method. PEDOT(PSS) solid contact is covered by PVC based H+‐selective membrane. The obtained coulometric signal demonstrates that the cumulated charge can be amplified by increasing the capacitance of solid contact. SCISEs covered with spin‐coated membrane behave faster amperometric response than electrodes with drop‐cast membrane. In contrast to earlier works, the amperometric response and impedance spectrum demonstrates H+ transfer through SCISEs is independent from the thickness of membrane. The exceptional behavior of PANI(Cl) H+‐SCISEs shows that the capacitance estimated from impedance spectrum at low frequency 10 mHz and coulometric signal of PANI(Cl) based SCISEs is influenced by the applied potentials, whereas PEDOT(PSS) solid contact is independent from the chosen applied potentials. Furthermore, preliminary investigations of coulometric signal transduction on flexible pH sensor implies its potential applications in wearable sensors for sweat ion concentration detection. [ABSTRACT FROM AUTHOR]

We first reported that polyvinylpyrrolidone-protected graphene was dispersed well in water and had good electrochemical reduction toward [O.sub.2] and [H.sub.2][O.sub.2]. With glucose oxidase (GOD) as an enzyme model, we constructed a novel polyvinylpyrrolidone-protected graphene/polyethylenimine-functionalized ionic liquid/ GOD electrochemical biosensor, which achieved the direct electron transfer of GOD, maintained its bioactivity and showed potential application for the fabrication of novel glucose biosensors with linear glucose response up to 14 mM.

Solid contact potassium-selective electrodes with the internal ion-to-electron transduction layer composed of plasticized poly(vinyl chloride) (PVC) and 2-20% (m/m) of polyaniline (PANI) nanoparticles, with the mean particle size of 8 nm, have been studied in this paper. UVvis measurements in pH buffer solutions between pH 0 and 12 show that the electrically conducting emeraldine salt (ES) form of PANI has exceptionally good pH stability. Membranes of PANI nanoparticles were mainly in the ES form even at pH 12, in contrast to electrochemically prepared PANI(CI) films, which are converted completely to the nonconducting form already at pH 6. Long-term UV--vis measurements with the PANI membranes in contact with aqueous buffer solution at pH 7.5 showed no degradation of the ES form. The PANI nanoparticles are homogenously mixed in the PVC-based solid contact (SC) layer. Only the uppermost part of the SC layer is to a minor extent dissolved in the outer potassium-selective PVC membrane. This enabled the preparation of geometrically well-defined inner SC layers, thus improving the reproducibility of the solid contact electrodes and resulting in good mechanical strength between the inner and outer membranes.

A novel method for pH measurements between pH 7.5 and 10.4 is reported in this paper. The method combines Raman spectroscopy and the automated sequential injection analysis system (SIA) and makes use of the acid base properties of a commercially available water dispersion of polyaniline (PANI) nanoparticles with a mean particle size of 46 nm. The useful pH range of the PANI nanoparticles is broader than for conventional acid-base indicators, due to the 1:2 reaction stoichiometry of the proton-ligand complex of the nanoparticles. The pH measurements were conducted with the 633-nm laser excitation wavelength by calculating the difference between the Raman intensities of the primary and reference wavenumbers. In this study, the pH-sensitive CH=CH stretching band at 1422 [cm.sup.-1] and C-H in-plane bending band of the quinoid form at 1163 [cm.sup.-1] were chosen as the primary wavenumbers. The presented method is fast and allows pH to be measured with a precision of 0.2 pH unit. The advantage of the proposed method is that the hysteresis effect, which is usually observed for PANI films, can be overcome with the PANI nanoparticles, because a fresh nanoparticle solution is used in each measurement. It should be pointed out, that this work is a fundamental study showing the applicability of Raman spectroscopy in combination with the SIA technique for pH measurements in specific applications, where the conventional glass pH electrode cannot be used.