Premium
Impedance Spectroscopy as a Tool for Chemical and Electrochemical Analysis of Mixed Conductors: A Case Study of Ceria
Author(s) -
Lai Wei,
Haile Sossina M.
Publication year - 2005
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/j.1551-2916.2005.00740.x
Subject(s) - dielectric spectroscopy , nyquist plot , partial pressure , ionic bonding , enthalpy , analytical chemistry (journal) , chemistry , ionic conductivity , electrolyte , ion , materials science , oxygen , thermodynamics , electrochemistry , electrode , physics , organic chemistry , chromatography
The AC impedance response of mixed ionic and electronic conductors (MIECs) is derived from first principles and quantitatively compared with experimental data. While the approach is not entirely new, the derivation is provided in a unified and comprehensive manner. Using Sm 0.15 Ce 0.85 O 1.925–δ with Pt electrodes as a model system, a broad spectrum of electrical and thermodynamic properties is extracted solely from the measurement of impedance spectra over wide oxygen partial pressure and temperature ranges. Here, the oxygen partial pressure was varied from air [ p o 2 =0.21 atm] to H 2 [ p o 2 =10 −31 atm], and the temperature was varied from 500° to 650°C. It was essential for this analysis that the material under investigation exhibit, under some conditions, purely ionic behavior and, under others, mixed conducting behavior. The transition from ionic to mixed conducting behavior is recognizable not only from the oxygen partial pressure dependence of the total conductivity but also directly from the shape of the impedance spectra. Within the electrolytic regime, the impedance spectra (presented in Nyquist form) take the shape of simple, depressed arcs, whereas within the mixed conducting regime (under reducing conditions), the spectra exhibit the features associated with a half tear‐drop‐shaped element. Parameters derived from quantitative fitting of the impedance spectra include the concentration of free electron carriers, the mobilities and activation energies for both ion and electron transport, the electrolytic domain boundary, and the entropy and enthalpy of reduction. In addition, the electrochemical behavior of O 2 and H 2 at the Pt∣ceria interface has been characterized from these measurements. Under oxidizing conditions, the data suggest an oxygen electrochemical reaction that is rate limited by the dissociated adsorption/diffusion of oxygen species on the Pt electrode, similar to Pt∣YSZ (yttria‐stabilized zirconia). Under reducing conditions, the inverse of the electrode resistivity obeys adependence, with an activation energy that is similar to that measured for the electronic conductivity. These results suggest that ceria is electrochemically active for hydrogen electro‐oxidation and that the reaction is limited by the rate of removal of electrons from the ceria surface.