4.8 Article

Solid Contact Ion-Selective Electrodes with a Well-Controlled Co(II)/Co(III) Redox Buffer Layer

Journal

ANALYTICAL CHEMISTRY
Volume 85, Issue 19, Pages 9350-9355

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ac4022117

Keywords

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Funding

  1. National Science Foundation [OISE CHE-0809328]
  2. MRSEC program [DMR-0212302]
  3. Direct For Mathematical & Physical Scien
  4. Division Of Chemistry [0809328] Funding Source: National Science Foundation

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Solid contact ion-selective electrodes (ISEs) typically have an intermediate layer between the ion-selective membrane and the underlying solid electron conductor that is designed to reduce the irreproducibility and instability of the measured electromotive force (emf). Nevertheless, the electrode-to-electrode reproducibility of the emf of current solid contact ISEs is widely considered to be unsatisfactory. To address this problem, we report here a new method of constructing this intermediate layer based on the lipophilic redox buffer consisting of the Co(III) and Co(II) complexes of 1,10-phenanthroline ([Co(phen)(3)](3+/2+)) paired with tetrakis(pentafluorophenyl)borate as counterion. The resulting electrodes exhibit emf values with an electrode-to-electrode standard deviation as low as 1.7 mV after conditioning of freshly prepared electrodes for 1 h. While many prior examples of solid contact ISEs also used intermediate layers that contained redox active species, the selection of a balanced ratio of the reduced and oxidized species has typically been difficult and was often ignored, contributing to the emf irreproducibility. The ease of the control of the [Co(phen)(3)](3+)/[Co(phen)(3)](2+) ratio explains the high emf reproducibility, as confirmed by the emf decrease of 58 mV per 10-fold increase in the ratio of the reduced and oxidized redox buffer species. Use of a gold electrode modified with a self-assembled 1-hexanethiol monolayer as underlying electron conductor suppresses the formation of a water layer and results in an electrode-to-electrode standard deviation of E degrees of 1.0 mV after 2 weeks of exposure to KCl solution.

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