Electrode reaction and microstructure of La0.6Sr0.4CoO3−δ thin films

Dense La_0.6Sr_0.4CoO_3−δ film electrodes were deposited by pulsed laser deposition (PLD) on Ce_0.9Gd_0.1O_1.95 electrolytes. The grain size of one film was 300–500 nm, and the other was 30–50 nm. DC polarization and AC impedance measurements were performed at 873 K–1073 K in O₂–Ar gas mixtures. From investigations of the electrochemical capacitances, the rate determining process for both electrodes were confirmed to be the surface reaction. The analyses in the electrochemical resistance revealed that the oxygen adsorption/desorption rate was faster on the electrode with smaller grain size. DC responses agreed with AC results, so the current density on the nano-grain electrode was larger by half an order than those of the sub-micron-grain electrode. Under a dilute oxygen atmosphere, the rate determining step transferred from a surface reaction to a gas phase diffusion.     

Behaviour of a dense In2O3/ YSZ electrode in oxygen containing atmospheres

A study of electrical and electrochemical properties of a dense In₂O₃ electrode in contact with a single crystal YSZ electrolyte was carried out by d.c. and a.c. methods. As a result, it was found that dense In₂O₃ electrodes have high electrical conductivity but very low electrochemical activity. In a vicinity of the equilibrium potential and under the anodic polarisation, the rate of Faraday reaction at the In₂O₃ electrodes was as low as to consider the electrode a blocking one. The blocking properties of the In₂O₃ electrodes were used to measure the hole conductivity of the YSZ electrolyte in the temperature range between 795 to 1163 K and oxygen partial pressure from 1 to 10⁵ Pa. A comparison with the literature data confirmed that the dense In₂O₃ electrode blockes the ionic transfer through the YSZ. A set of experiments indicated that the oxygen exchange between the indium oxide surface presented to the oxygen containing gaseous phase and this phase is very poor. A route of the electrode process at O₂, In₂O₃ / YSZ electrode was proposed a limiting stage of which is the discharge of the oxygen ions to the atomic oxygen adsorbed on the electrode surface: $$O_0 ^x \left( {In_2 O_3 } \right)_s = V_0 ^{ \bullet \bullet } \left( {In_2 O_3 } \right)_s + O_{ad} \left( {In_2 O_3 } \right)_s + 2e'\left( {In_2 O_3 } \right).$$ The polarisation resistance decreases when platinum or the praseodymium oxide is deposited on the surface of the In₂O₃ electrodes. The cathodic polarisation also increases the electrochemical activity of the electrodes. Both the establishment of the steady state of the electrode under polarisation and the recovery of the equilibrium state by the electrode are very long processes, which are probably related to the diffusion mechanism by which the stoichiometry of the indium oxide is changed.     

(La0.75Sr0.25)(Cr0.5Mn0.5)O3/YSZ composite anodes for methane oxidation reaction in solid oxide fuel cells

The synthesis and performance of (La_0.75Sr_0.25)(Cr_0.5Mn_0.5)O₃/Y₂O₃–ZrO₂ (LSCM/YSZ) composites are investigated as alternative anodes for the direct utilization of methane (i.e., natural gas) in solid oxide fuel cells. Addition of YSZ phase greatly improves the adhesion and reduces the electrode polarization resistance of the LSCM/YSZ composite anodes. LSCM/YSZ composite anodes show reasonably good performance for the methane oxidation reaction in wet CH₄ and the best electrode performance was achieved for the composite with LSCM contents of 50–60 wt.% with polarization resistances of 2–3 Ω cm² in 97% CH₄/3% H₂O at 850 °C. The electrode impedance for the methane oxidation in wet CH₄ on the LSCM/YSZ composite anodes was characterized by three separable arcs and the electrode behavior could be explained based on the ALS model for the reaction on the MIEC electrode. The results indicate that electrocatalytic activity of the LSCM/YSZ composite anodes for the methane oxidation is likely limited by the oxygen vacancy diffusion in the substituted lanthanum chromite-based materials.     

Simultaneous removal of nitrogen oxides and diesel soot particulate in nano-structured electrochemical reactor

Simultaneous decomposition of nitrogen oxides (NO_x) and solid state graphite particles were carried out using a 8 mol% Y₂O₃ doped ZrO₂ (YSZ) based electrochemical reactor with a nano-structured NO_x selective multilayer cathode and an oxidative porous anode. The ceramic electrochemical cell was prepared by screen-printing a Pt and a NiO–YSZ pastes as cathode layers and a 12 CaO7Al₂O₃–Pt paste as an anode layer on the YSZ electrolyte, respectively. Simultaneous decomposition of NO_x and graphite particles was investigated using the cell with coated graphite particles on the surface of the 12 CaO7Al₂O₃–Pt composite anode in 1000 ppm NO_x–He gas flow under applying DC voltage at 475 °C. The coated graphite particles at the anode were removed completely with 80% NO_x decomposition by electrochemical reactions.     

Electrode materials, interface processes and transport properties of yttria-doped zirconia

The kinetics of the oxygen exchange reactions at the electrodes of a galvanic cell using yttria-doped zirconia single crystals (9.5 mole-% Y₂O₃) as solid electrolyte and Pt or Ag as electrode materials was studied by complex impedance spectroscopy. The electrode resistance when using silver was found to have negligible values over the temperature range 180 – 900 °C. In agreement with these results, oxygen sensors were tested successfully at temperatures as low as 200 °C. According to the performance of silver as electrode material, an electrochemical method was developed to determine the oxygen diffusion coefficient in doped zirconia. The results obtained, compared to those of conductivity and oxygen tracer diffusion measurements, have allowed us to obtain information both on the structure of the defects in yttria-doped zirconia and on the correlation factor. Paper presented at the 4th Euroconference on Solid State Ionics, Renvyle, Galway, Ireland, Sept. 13–19, 1997     

A review of recent progress in sensing of gas concentration by impedance change

The intent of this paper is to establish the state of the art of impedance-based gas sensors. This sensor type holds promise for accurate detection of gaseous species at single parts per million and below. Impedance-based sensors do not require reference air to function, but do require calibration. Progress in the development of impedancemetric sensors for the detection of NO_x, H₂O, hydrocarbons, and CO is reviewed. Sensing electrodes typically consist of a noble metal or a metal oxide. YSZ is the preferred electrolyte material. Counter electrodes of Pt were common in asymmetric cells. These sensors typically operate at 500–700 °C and are interrogated at 10 Hz or less. Selectivity of these sensors remains a challenge especially in lean environments. Stability is an infrequently discussed yet important concern. Equivalent circuit analysis has shed light on various detection mechanisms. The impedance changes due to analyte gases are exhibited in parameters that represent the low frequency behavior of the electrochemical system. Although the search for a detailed mechanism continues, the change in impedance due to a specific gas is generally attributed to transport processes such as adsorption and charge transfer.     

Thermal desorption study of Oxygen adsorption on Pt, Ag & Au films deposited on YSZ

The Thermal Desorption or Temperature Programmed Desorption (TPD) technique has been used for the study of oxygen adsorption on Pt, Ag and Au catalyst films deposited on YSZ. The catalyst film was deposited on the one side of the YSZ specimen while on the other side gold counter and reference electrodes were deposited, constructing a three-electrode electrochemical cell similar to those used in Electrochemical Promotion studies. Oxygen adsorption has been carried out either by exposing the samples to gaseous oxygen (gas phase adsorption) or by the application of a constant current between the catalyst/working electrode and the counter electrode (electrochemical adsorption) or by mixed gas phase and electrochemical adsorption. Oxygen adsorption was carried out at temperatures between 200 and 480 °C. After exposure to gaseous oxygen, normal adsorbed atomic oxygen species have been observed on Pt and Ag surfaces while there was no detectable amount of adsorbed oxygen on Au. Electrochemical O²⁻ pumping to Pt, Ag and Au catalyst films creates strongly bonded “backspillover” anionic oxygen, along with the more weakly bonded atomic oxygen. Electrochemical O²⁻ pumping to Pt, Ag and Au catalyst films in presence of preadsorbed oxygen creates strongly bonded “backspillover” anionic oxygen, with a concomitant pronounced lowering of the T_p of the more weakly bound preadsorbed atomic oxygen. The two oxygen species co-exist on the surface. The activation energy for oxygen desorption or, equivalently, the binding strength of adsorbed oxygen was found to decrease linearly with increasing catalyst potential, for all three metal electrodes. Paper presented at the 4th Euroconference on Solid State Ionics, Renvyle, Galway, Ireland Sept. 13–19, 1997     

Electrical parameters of Schottky contacts in CaCu3Ti4O12 thin film capacitors

CaCu₃T_i4O₁₂ (CCTO) thin films were grown by pulsed laser deposition on Pt and La_0.9Sr_1.1NiO₄ (LSNO) bottom electrodes. The electrical characteristics of the CCTO/Pt and CCTO/LSNO Schottky junctions have been analyzed by impedance spectroscopy, capacitance–voltage (C–V) and current–voltage (I–V) measurements as a function of frequency (40 Hz–1 MHz) and temperature (300–475 K). Similar results were obtained for the two Schottky diodes. The conduction mechanism through the Schottky junctions was described using a thermionic emission model and the electrical parameters were determined. The strong deviation from the ideal I–V characteristics and the increase in capacitance at low frequency for ?0.5 V bias are in agreement with the presence of traps near the interfaces. Results point toward the important effect of defects generated at the interface by deposition of CCTO.     

Electrical degradation of porous and dense LSM/YSZ interface

Electrochemical cells formed by the interface between dense and porous lanthanum strontium manganate (LSM) and yttria stabilized zirconia (YSZ) were submitted to annealing temperatures varying from 1373 K to 1673 K for 200 h and studied by Impedance Spectroscopy (IS) in order to investigate how the high annealing temperature can modify the contact between LSM/YSZ and to which extension these changes influence the electrical behavior of dense and porous LSM electrodes before and after the formation of insulating phases. Up to 1473 K the annealing process did not lead to substantial electrical behavior modifications at the LSM/YSZ interfaces for both porous and dense electrodes. IS measurements show two capacitive semicircles, the best fitting of impedance data brings to an equivalent circuit constituted by a serial combination of the electrolyte resistance and two parallel combinations of a resistance and a constant phase element, CPE. The higher frequency semicircles, HF, were attributed to the diffusion of oxide ions from the interface LSM/YSZ to the oxide ion vacancies located at the electrolyte surface. The semicircle at lower frequency, LF, will be ascribed to the oxygen species adsorption and diffusion in the LSM. At 1473 K the only changes recorded are related with the sinterization process of the porous electrodes. Over of 1473 K, the resistance contributions increased largely, especially for porous electrodes, and one additional semicircle was observed. This semicircle was associated to the oxygen diffusion process at the new insulating phases formed from YSZ and LSM solid state reactions. Porous and dense electrodes exhibited different rates for the degradation process. The porous electrode degraded faster than the dense one, probably because of the morphological effects as grain growth and their coalescence during annealing at higher temperatures.     

Electrochemical and structural study of neodymium nickelate thick film deposited by spin coating on an oxyapatite electrolyte

The electrochemical characteristics of an Nd₂NiO₄ cathode, synthesized using the citric acid-nitrate combustion method and symmetrically deposited by spin coating on both surfaces of an La_9.33Si_5.3Al_0.7O_25.65 (LSAO) electrolyte, were studied using AC impedance spectroscopy. It was found that, varying the temperature (600 to 850 °C) and the oxygen partial pressure (0.2–10^?7 atm), the impedance characteristics of the electrode could be determined by three different processes. Said processes were ionic conduction in the electrode bulk, interfacial charge transfer, and gas-phase diffusion, all of which are based on the temperature and oxygen partial pressure dependence on the polarization resistance, which is associated with each individual processes as well as on the corresponding capacitance values.     

Ba0.5Sr0.5Co0.8Fe0.2O3−δ thin film microelectrodes investigated by impedance spectroscopy

The electrochemical properties of geometrically well-defined Ba_0.5Sr_0.5Co_0.8Fe_0.2O_3−δ (BSCF) microelectrodes have been investigated by impedance spectroscopy. The microelectrodes of 20–100 μm diameter and 100 nm thickness were prepared by pulsed laser deposition (PLD), photolithography and argon ion beam etching. The oxygen reduction reaction at these model electrodes is limited by interfacial processes, i.e. by the oxygen surface exchange and/or by the transfer of oxide ions across the electrode/electrolyte boundary, whereas the resistance associated with the transport of oxide ions through the bulk of the thin film electrode is negligible. The experiments revealed an extremely low absolute value of the electrochemical surface exchange resistance of only 0.09 (± 0.03) Ω cm² at 750 °C in air, which is more than a factor of 50 lower than the corresponding value measured for La_0.6Sr_0.4Co_0.8Fe_0.2O_3−δ (LSCF) microelectrodes of the same geometry. The dependence of this and other electrochemical quantities such as the chemical bulk capacitance or the BSCF/YSZ interfacial resistance on temperature has been studied between 500 and 750 °C.     

Electrical impedance spectroscopy of ionic liquid 1-ethyl-3-methylimidazolium methanesulfonate (ECOENG™ 110)

Ionic liquid “ECOENG? 110”, a promising electrolyte for electrochemical devices, was investigated by impedance spectroscopy. Metallic electrodes (Pt, Cu, Ag, and Mo) as well as carbon were used for the electrochemical characterization. The dependences of the real and imaginary impedance, polarization resistance and electrochemical capacity of the double layer on the electrode potential were investigated using electrical equivalent circuits of R₁(QR₂) and R₁[Q(R₂W)] types.     

Rate limiting steps of the porous La0.6Sr0.4Co0.8Fe0.2O3−δ electrode material

The electrode reaction of porous La_0.6Sr_0.4Co_0.8Fe_0.2O_3?δ films deposited onto Ce_0.9Gd_0.1O_1.95 (CGO) was investigated by impedance spectroscopy within the temperature and oxygen partial pressure (pO₂) ranges of 500 ≤ T ≤ 700 °C and 10^? 4 < pO₂ < 1 atm, respectively, using Ar and He as gas carriers. The electrochemical impedance spectroscopy (EIS) measurements reveal a high frequency (HF) and a low frequency (LF) regions in the Nyquist plane. The high frequency (HF) region was fitted with a Warburg-type impedance element, and the low frequency (LF) region was reproduced with a resistance in parallel to a constant phase element. Both, the slight dependence of the polarization resistance (R_W) and the small variation of the apex frequency (f_v) of the HF Warburg-type element, on pO₂, suggest that this contribution corresponds to the oxygen diffusion in the bulk of the La_0.6Sr_0.4Co_0.8Fe_0.2O_3?δ electrode material. The variation of the polarization resistance of the LF region (R_rcpe) with pO₂ indicates that as T increases, the limiting step evolves from dissociative oxygen adsorption to oxygen gas diffusion in the pores of the mixed ionic/electronic conductor (MIEC) electrode.     

Complex admittance study of β-PbF2 single crystals

The complex admittance of β-PbF₂ single crystals between two inert blocking electrodes was studied from R.T. to 730 K. A strong frequency dependence was observed over the frequency range 0.1 Hz–100 kHz. The bulk conductances were obtained from the frequency independent conductances. With increasing temperature the electrode discharge processes are dominated by a diffusional impedance.     

Electrode reaction at Pt,O2(g)/stabilized zirconia interfaces. Part I: Theoretical consideration of reaction model

This study aims to make clear the reaction kinetics at Pt, O₂(g)/zirconia electrodes in the oxygen partial pressure, P_O2, of ∼ 10⁻⁴ − 1 atm at ∼ 400–∼800°C. By a critical review on the preceding studies, problems were pointed out in the application of the Langmuir adsorption isotherm to the P_O2 dependence of electrode conductance, in the assumption of electric double layer at the electrode interface, and of the inconsistency between the recent reaction model of surface diffusion controlled kinetics and the absolute rate theory. It was shown that the charge transfer kinetics cannot be the rate determining step (RDS) of the electrode reaction. The possible RDS was concluded to be either (i) dissociative adsorption of oxygen molecules on the Pt surface or (ii) surface diffusion of O_ad atoms on the Pt surface to the Pt/zirconia contact. The diffusion of O_ad atoms on the Pt surface was considered to be proportional to θ(1−θ)(∂μ_O/∂x), where θ is the occupancy of O_ad atoms on Pt and μ_O is the oxygen chemical potential on the Pt surface. The rate equation, current-potential relationship, and the electrode conductivity, σ_E, were calculated for the cases the RDS is (i) and (ii), respectively. By comparing the calculated σ_E versus log P_O2 relationship with the reported ones, it was shown that the RDS is (i) for T ≲ 500°C and is (ii) for T ≳ 600°C. In the former case, σ_E is essentially constant irrespective to P_O2, and in the latter case, σ_E maximum appears on the σ_E versus log P_O2 relations.     

Kinetic study on LiFePO<Subscript>4</Subscript>-positive electrode material of lithium-ion battery

LiFePO₄-positive electrode material was successfully synthesized by a solid-state method, and the effect of storage temperatures on kinetics of lithium-ion insertion for LiFePO₄-positive electrode material was investigated by electrochemical impedance spectroscopy. The charge-transfer resistance of LiFePO₄ electrode decreases with increasing the storage temperatures. This suggests that it has a high electrochemical activity at high temperature. The diffusion coefficient of lithium ion is greatly increased with increasing the storage temperatures, indicating that the kinetics of Li⁺ and electron transfer into the electrodes were much fast at high storage temperature.     

The electrode model system Pt(O2)|YSZ: Influence of impurities and electrode morphology on cyclic voltammograms

This study is focused on the influence of impurities and electrode morphology on cyclic voltammograms (CV) of one of the most prominent solid state electrode systems, Pt(O₂)|YSZ, exemplifying the difficulties in unequivocal interpretation of CV in the solid state in general. By investigating differently prepared electrodes—either by Pt paste or pulsed laser deposition (PLD)—with and without an Si containing additive, the impact of both effects can be separated. For characterisation of the sample SEM, XRD, EDX, Tof-SIMS, XPS, and XPEEM have been used. We demonstrate that the presence of impurities can change the shape of CV and even cause peaks, a fact which has not been considered so far. The processes which theoretically can cause a CV peak in the electrode system Pt(O₂)|YSZ are discussed. We reconsider the information unambiguously obtainable from CV studies, and we comment on the controversial questions of the formation of interface Pt oxide and the appearance of spillover oxygen in CV studies. A compact commented survey of literature on CV studies of the system Pt(O₂)|YSZ is given.     

Co-electrolysis of CO2 and H2O in solid oxide cells: Performance and durability

This study examines the initial performance and durability of a solid oxide cell applied for co-electrolysis of CO₂ and H₂O. Such a cell, when powered by renewable/nuclear energy, could be used to recycle CO₂ into sustainable hydrocarbon fuels. Polarization curves and electrochemical impedance spectroscopy were employed to characterize the initial performance and to break down the cell resistance into the resistance for the specific processes occurring during operation. Transformation of the impedance data to the distribution of relaxation times (DRT) and comparison of measurements taken under systematically varied test conditions enabled clear visual identification of five electrode processes that contribute to the cell resistance. The processes could be assigned to each electrode and to gas concentration effects by examining their dependence on gas composition changes and temperature.This study also introduces the use of the DRT to study cell degradation without relying on a model. The durability was tested at consecutively higher current densities (and corresponding overpotentials). By analyzing the impedance spectra before and after each segment, it was found that at low current density operation (− 0.25 A/cm² segment) degradation at the Ni/YSZ electrode was dominant, whereas at higher current densities (− 0.5 A/cm² and − 1.0 A/cm²), the Ni/YSZ electrode continued to degrade but the serial resistance and degradation at the LSM/YSZ electrode began to also play a major role in the total loss in cell performance. This suggests different degradation mechanisms for high and low current density operation.     

Preparation and electrochemical characterisation of supporting SOFC–Ni–YZT anodes

Symmetrical cells consisting of Ni–Y_0.20Ti_0.18Zr_0.62O_1.90 (Ni–YZT) cermet electrodes on a Ni–YSZ support have been investigated with respect to the hydrogen/water partial pressures. Impedance spectra at open circuit potential were obtained as function of temperature and analysed in terms of a fractal finite length Gerischer Impedance. For fine and coarse microstructures of the Ni–YZT electrodes, a consistent set of model parameters could be obtained. The results indicate that surface diffusion rather than bulk diffusion plays a role in the hydrogen/water reaction but also that a fine-grained fraction in the mixed conducting YZT phase is advantageous for the overall electrode performance and the surface exchange reaction.     

Impedance spectrum of a single grain boundary in yttrium stabilized zirconia

Impedance measurements are reported for a bicrystal and single crystals of yttrium-stabilized ZrO₂ (YSZ) over the range from 100 to 10⁷ Hz, and for temperatures from 200 to 500°C in air. In addition to the impedances introduced by the conduction process within the grains and by charge transfer process at the electrodes, the grain-boundary introduced an additional impedance which was observed as an additional arc when the impedance was plotted in the complex plane. These data and an examination by both optical and scanning electron microscopy reveal the grain boundary to be a gap between the adjacent crystals, with occasional bridges of YSZ. These results illustrate the potential of impedance spectroscopy for studying intercrystalline interfaces in solid conductors.