Electrically conducting polymers (ECPs) are one of the most popular types of materials to interface ion-selective membranes (ISMs) with electron conducting substrates to construct solid contact ion-selective electrodes (SCISEs). For optimal ion-to-electron transduction and potential stability, the p-doped ECPs with low oxidation potentials such as PPy need to be generally in their conducting form along with providing a sufficiently hydrophobic interface to counteract the aqueous layer formation. The first criterion requires that the ECPs are in their oxidized state, but the high charge density of this state is detrimental for the prevention of the aqueous layer formation. We offer here a solution to this paradox by implementing a highly hydrophobic perfluorinated anion (perfluorooctane sulfonate, PFOS -) as doping ion by 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 2 which the oxidized form of the ECP becomes hydrophobic. The proof of concept is shown by using polypyrrole (PPy) films doped with PFOS -(PPy-PFOS) as the solid contact in K + -selective SCISEs (K + -SCISE). Prior to applying the plasticized poly(vinyl chloride) ISM, the oxidation state of the electrodeposited PPy-PFOS was adjusted by polarization to the known open circuit potential of the solid contact in 0.1 M KCl. We show that the pre-polarization results in a hydrophobic PPy-PFOS film with a water contact angle of 97±5º, which effectively prevents the aqueous layer formation under the ISM. Under optimal conditions the K + -SCISEs had a very low standard deviation of E 0 of only 501.0±0.7 mV that is the best E 0 reproducibility reported for ECP-based SCISEs.

We report the synthesis and analytical application of the first Cu2+‐selective synthetic ion channel based on peptide‐modified gold nanopores. A Cu2+‐binding peptide motif (Gly‐Gly‐His) along with two additional functional thiol derivatives inferring cation‐permselectivity and hydrophobicity was self‐assembled on the surface of gold nanoporous membranes comprising of about 5 nm diameter pores. These membranes were used to construct ion‐selective electrodes (ISEs) with extraordinary Cu2+ selectivities, approaching six orders of magnitude over certain ions. Since all constituents are immobilized to a supporting nanoporous membrane, their leaching, that is a ubiquitous problem of conventional ionophore‐based ISEs was effectively suppressed.

The irreproducibility of the standard potential (E°) is probably the last major challenge for the commercialization of solid-contact ion-selective electrodes (SCISEs) as single-use or wearable sensors. To overcome this issue, we are introducing for the first time a perfluorinated alkanoate side chain functionalized poly(3,4-ethylenedioxythiophene) (PEDOTF) as a hydrophobic SC in potassium-selective electrodes (K-SCISEs) based on plasticized poly(vinyl chloride). The SC incorporates the tetrakis(pentafluorophenyl)borate (TFAB–) anion, which is also present as a lipophilic additive in the ion-selective membrane (ISM), thus ensuring thermodynamic reversibility at the SC/ISM interface and improving the potential reproducibility of the electrodes. We show here that the PEDOTF-TFAB solid contact, which was prepolarized prior to the ISM deposition to either its half or fully conducting form (i.e. different oxidation states) in acetonitrile containing 0.01 M KTFAB, had a very stable open-circuit potential and an outstanding potential reproducibility of only ±0.5 mV (n = 6) for 1 h in the same solution after the prepolarization. This shows that the oxidation state of the highly hydrophobic PEDOTF-TFAB film (water contact angle 133°) is stable over time and can be precisely controlled with prepolarization. The SC was also not light sensitive, which is normally a disadvantage of conducting polymer SCs. After the ISM deposition, the standard deviation of the E° of the K-SCISEs prepared on glassy carbon was ±3.0 mV (n = 5), which is the same as that for conventional liquid contact K-ISEs. This indicates that the ISM deposition is the main source for the potential irreproducibility of the K-SCISEs, which has been overlooked previously.

The two most promising approaches for preparing solid contacts (SCs) for polymeric membrane based ion‐selective electrodes (ISEs) are based on the use of large surface areas conducting materials with high capacitance (e. g., various carbon nanotubes) and redox active materials (e. g. conducting polymers). While many of the essential requirements for the potential stability of SCISEs were addressed, the E0 reproducibility and its predictability, that would enable single use of such electrodes without calibration is still a challenge, i. e., the fabrication of electrodes with sufficiently close E0 and slope values to enable the characterization of large fabrication batches through the calibration of only a small number of electrodes. The most generic solution seems to be the adjustment of the E0 potential by polarization prior to the application of the ion‐selective membrane. This approach proved to be successful in case of conducting polymer‐based solid contacts, but has to be still explored for capacitive solid contact based ISEs, which is the purpose of this paper. We have chosen a well‐established highly lipophilic multi‐walled carbon nanotube (MWCNT), i. e. octadecane modified MWCNT (OD‐MWCNT), that is investigated in the comparative context of a similarly lipophilic conducting polymer solid contact (a perfluorinated alkanoate side chain functionalized poly(3,4‐ethylenedioxythiophene)). While, the OD‐MWCNT based SCISEs had inherently small standard deviation of their E0 values (less than 5 mV) this could be further improved by external polarization and short circuiting the SCISEs.

Solid-contact ion-selective electrodes (SCISEs) can overcome essential limitations of their counterparts based on liquid contacts. However, attaining a highly reproducible and predictable E 0 , especially between different fabrication batches, turned out to be difficult even with the most established solid-contact materials, i.e., conducting polymers and large-surface-area conducting materials (e.g., carbon nanotubes), that otherwise possess excellent potential stability. An appropriate batch-to-batch E 0 reproducibility of SCISEs besides aiding the rapid quality control of the electrode manufacturing process is at the core of their “calibration-free” application, which is perhaps the last major challenge for their routine use as single-use “disposable” or wearable potentiometric sensors. Therefore, here, we propose a new class of solid-contact material based on the covalent functionalization of multiwalled carbon nanotubes (MWCNTs) with a chemically stable redox molecule, (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO). This material combines the advantages of (i) the large double-layer capacitance of MWCNT layers, (ii) the adjustable redox couple ratio provided by the TEMPO moiety, (iii) the covalent confinement of the redox couple, and (iv) the hydrophobicity of the components to achieve the potential reproducibility and stability for demanding applications. The TEMPO-MWCNT-based SC potassium ion-selective electrodes (K + -SCISEs) showed excellent analytical performance and potential stability with no sign of an aqueous layer formation beneath the ion-selective membrane nor sensitivity toward O 2 , CO 2 , and light. A major convenience of the fabrication procedure is the E 0 adjustment of the K + -SCISEs by the polarization of the TEMPO-MWCNT suspension prior to its use as solid contact. While most E 0 reproducibility studies are limited to a single fabrication batch of SCISEs, the use of prepolarized TEMPO-MWCNT resulted also in an outstanding batch-to-batch potential reproducibility. We were also able to overcome the hydration-related potential drifts for the use of SCISEs without prior conditioning and to feature application for accurate K + measurements in undiluted blood serum.