Mechanistic origin of the time-dependence of the open-circuit voltage of a galvanic cell involving a ternary or higher compound. Issue 28 (12th July 2021)

• Record Type: Journal Article
• Authors: Yoo, Han-Ill; Kim, Jihye; Joo, Wonhyo; Martin, Manfred
• Is Part Of: Physical chemistry chemical physics. Volume 23:Issue 28(2021)
• Page Start: 15119
• Page End: 15126
• Publication Date: 2021-07-12
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/d1cp01793d
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : The open-circuit voltage U of a galvanic cell involving a multinary, e.g ., SrTi1− x Al x O3− Δ is rendered time-dependent by introducing a secondary ionic carrier, e.g ., H + in addition to the primary one, O 2−, due to decoupled relaxation of H and O. Abstract : It has previously been predicted [H.-I. Yoo and M. Martin, Phys. Chem. Chem. Phys., 2010, 12, 14699] and observed [E. Kim, et al., Solid State Ionics, 2013, 235, 22] that the open-circuit voltage U of a galvanic cell, involving a ternary or higher compound with more than one kind of mobile ionic carrier, is path- and time-dependent upon imposition or removal of the mobile components' chemical potential differences, in contradistinction to the cell involving a binary compound. This has been attributed [H.-I. Yoo and M. Martin, Phys. Chem. Chem. Phys., 2010, 12 14699; J.-Y. Yoon, et al., Solid State Ionics, 2012, 213, 22] to the decoupled redistributions of multiple mobile components or multi-fold relaxation. We hereby experimentally demonstrate with SrTi0.982 Al0.018 O3− Δ, known to have an appreciable water solubility depending on temperature, that introduction of a secondary ionic carrier H + in addition to the native O 2− indeed renders the otherwise time-independent U time-dependent; and that this phenomenon may, thus, be employed to probe the presence of a secondary ionic carrier, e.g., H + in addition to the primary O 2− in BaTi0.982 Al0.018 O3− Δ whose water solubility is yet to be known. The temporal behavior of U of SrTi0.982 Al0.018 O3− Δ subjected to the two fixed chemical potential differences, Δ μ O and Δ μ H, is precisely delineated in terms of two-fold relaxation of H and O, yielding their chemical diffusivity values, and consequently, the ambiguity with the EMF-method to determine the ionic transference numbers of a multinary compound is cleared away.