ABSTRACT
Liquid membrane type ion-selective electrodes (ISEs) provide one of the most versatile sensing methods because it is possible to customize the sensory elements to suit the structure of the analyte. A wealth of different synthetic and natural ionophores has been developed, in the past 30 years, for use in liquid membrane type ISEs for various inorganic and organic ions [1]. In extensive studies [2-4], the response mechanism of these ISEs has been interpreted in terms of thermodynamics and kinetics. However, there have been few achievements in the characterization of the processes occurring at the surface of ISEs at molecular level.
