Abstract

The Ag@AgCl/1-tetradecyl-3-methylimidazolium chloride (TMMCl) reported as an inorganic redox buffer for solid contact ion-selective electrodes (SC-ISEs) suffers from minimized specific area for an aggregation of Ag nanoparticles and decreased electron transfer for a presence of AgCl coating. Herein, a novel optimized inorganic redox buffer of r-GO/Ag@AgCl/TMMCl with improved capacitance and electron transfer behaving well as an effective ion-to-electron transducer for a SC-Ca2+-ISE has been highlighted. With reduced graphene oxide (r-GO) introduced as a substrate, the produced Ag nanoparticles as well as the subsequently synthesized core-shell Ag@AgCl nanomaterials display high dispersity with diameters decreased to 10–40 nm. Cyclic voltammetry with better redox reversibility and higher areas for the r-GO/Ag@AgCl/TMMCl verifies its improved redox capacitance and acceleration in electron transfer. Taking advantage of the r-GO/Ag@AgCl/TMMCl, the fabricated SC-Ca2+-ISE exhibits a near Nernst slope about 28.5 mV/dacade between potentials to Ca2+ concentrations ranging from 10−6 to 10−3M. Additionally, a diminished Rbc and Rct as well as an increased capacitance are also exemplified by the EIS and chronopotentiometric techniques, which would ensure a fast and stable potentiometric response. Moreover, the fabricated SC-Ca2+-ISE displays a good selectivity and water layer resistance. Thanks to the increased redox capacitance of the r-GO/Ag@AgCl/TMMCl, the fabricated SC-Ca2+-ISE demonstrates stable potentiometric response and good E0 reproducibility.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.