Calcium Manganite as Oxygen Electrode Materials for Reversible Solid Oxide Fuel Cell

For an efficient high-temperature reversible solid oxide fuel cell (RSOFC), the oxygen electrode should be highly active for the conversion between oxygen anions and oxygen gas. CaMnO 3Àd (CM) is a perovskite that can be readily reduced with the formation of Mn 3+ giving rise to oxygen defective phases. CM is examined here as the oxygen electrode for a RSOFC. CaMn 0.9 Nb 0.1 O 3Àd (CMN) with Nb doping shows superior electric conductivity (125 S cm À1 at 700 C) compared with CM (1–5 S cm À1 at 700 C) in air which is also examined for comparison. X-ray diffraction (XRD) data show that CM and CMN are compatible with the widely used yttria-stabilized zirconia (YSZ) electrolyte up to 950 C. Both materials show a thermal expansion coefficient (TEC) close to 10.8–10.9 ppm K À1 in the temperature range between 100–750 C, compatible with that of YSZ. Polarization curves and electrochemical impedance spectra for both fuel cell and steam electrolysis modes were investigated at 700 C, showing that CM presented a polarization resistance of 0.059 U cm 2 under a cathodic bias of À0.4 V while CMN gave a polarization resistance of 0.081 U cm 2 under an anodic bias of 0.4 V. The phase stability up to 900 C of these materials was investigated with thermogravimetric analysis (TGA) and variable temperature XRD.


Introduction
Renewable energy sources have attracted much attention in recent years to reduce the dependency on fossil fuels that cause pollutant gas emission and climate change. 1 The lack of synchronization between electricity production and consumption makes energy storage crucial for the grid to function effectively.A reversible solid oxide fuel cell (RSOFC) that incorporates the production of H 2 fuel from electricity via a solid oxide electrolysis cell (SOEC) and electricity generation via a solid oxide fuel cell (SOFC) could be an efficient and low-cost solution for energy conversion and storage.3][4] It is expected that through the combination of a high-temperature reactor and a high temperature electrolyser, the process will achieve an overall thermal conversion efficiency of 48-59% tray with a pestle and pre-calcined in a alumina crucible at 1000 C for 12 hours.Then the 20 gram admixture was ground in a planetary ball-mill at 300 rpm for 30 min for better mixing and then pelletized and red at 1300 C for 20 hours for the correct perovskite phase.The heating and cooling ramp rates were 10 C min À1 for both the calcination and nal ring state.The pellets were then crushed and ground using an agate mortar for characterization with thermogravimetric analysis (TGA) and room temperature X-ray diffraction (XRD).Dense pellets of dilatometry measurement were obtained by calcining the ball-milled powder at 1300 C for 20 hours and then cooling to room temperature at 1 C min À1 to avoid any cracking during the cooling process.The dimensions for the pellet were approximately 10 mm in diameter and 2 mm in thickness.The thermal expansion of the dense pellets was analyzed with a high-temperature dilatometer (Netzsch, DIL 402C) in a owing air atmosphere.The samples were heated and cooled to 900 C at a rate of 3 C min À1 and dwelled at 900 C for 1 hour.For the compatibility test between the materials and YSZ, the 1.0 g powder of CM(N) and 1.0 g YSZ was agate-mixed, pressed under 150 MPa and then calcined at 950 C for 5 hours at a ramp rate of 10 C min À1 .XRD was performed at room temperature on a PANalytical Empyrean diffractometer operated in reection mode using Cu-K a1 (wavelength: 1.5406 Å) radiation for the analysis of unit cell and structure.The XRD data were simulated with GSAS simulation soware, in order to determine the unit cell and arrangement of atoms in the materials.TGA was performed on a NETZSCH 49C thermo-gravimeter up to 900 C at a ramp rate of 10 C min À1 .
Pellets of 8% Y 2 O 3 -stabilized zirconia (8YSZ) powder were pressed uni-axially at a pressure of 80 MPa and calcined at 1500 C for 10 hours to give a >95% dense electrolyte.The electrolyte diameter was controlled to be 20 mm.In order to improve the adhesion between the electrode and electrolyte, the hand-ground powder was milled with zirconia balls ($1 mm in diameter) again at 650 rpm in isopropanol for 30 minutes in a planetary ball-mill to get the ne source powders for the fabrication of the electrode.High temperature XRD measurements were performed on a Panalytical diffractometer operated in reection mode using a Mo target (wavelength of K a1 ¼ 0.7093 Å and K a2 ¼ 0.71359 Å).The samples were stabilized at each temperature for 15 minutes before each scanning in the 2q range from 10 to 50 .Three grams of the mixed powder was mixed with a vehicle containing polyvinyl butyral (PVB) and sh oil to make the slurry that would be applied onto a dense 8YSZ electrolyte through screen printing.Three screenprinted layers with intermediate dryings at 80 C were utilized to give an electrode of around 20 mm thickness aer ring.A good bonding between the electrode and electrolyte was obtained aer calcination at 950 C for 2 hours at a ramp rate of 3 C min À1 .
Two congurations of cells were used to test the performance of the air electrode in this paper.A symmetrical cell contains two identical oxygen electrodes on both sides of the 8YSZ electrolyte of 1.8 mm in thickness and 2 cm in diameter.The symmetrical cells were employed to measure the polarization resistance of the electrode in static air in the temperature range between 550 C and 700 C. The other conguration, called a three-electrode system, was composed of an oxygen electrode, a Ni(O)-YSZ fuel electrode and a reference electrode on the edge of the electrolyte ($1.0 mm thick).The Ni(O)-YSZ fuel electrode (13 mm in diameter) was prepared by screen printing of the slurry containing 55 wt% NiO and 45 wt% YSZ onto the electrolyte plus a ring at 1350 C for 3 hours.A (La 0.8 Sr 0.2 ) 0.95 MnO 3 slurry was painted onto the edge of the electrolyte and dried at 80 C for 30 minutes and then red at 950 C for two hours along with the ring of the oxygen electrode.A silver wire (0.5 mm thick) was bundled the LSM coating and then red at 700 C again to provide the reference.The humidied gas (N 2 -50% H 2 O-3% H 2 ) in the fuel electrode was produced by injecting deionised water into an evaporator to mix with the nitrogen carrier gas containing 5% H 2 , as described previously. 2 Silver paste was used for the current collection for both the symmetrical-cell and three-electrode testing.The impedance was measured with a Solartron electrochemical workstation equipped with a lock-in frequency analyzer (Solartron 1260) with a sine wave of 10 mV.The three-electrode testing procedure commenced with sealing of the fuel electrode side of cells to the alumina tube of the testing jig, which was then placed in a vertical furnace.Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) of the powders and tested samples are taken on a Jeol 6700F microscope and Jeol 2011, respectively.

Crystal structure and compatibility with YSZ
The crystal structure of CM and CMN was regarded as an orthorhombic structure, 12,15,17 with the cell parameters of O2a cubic Â 2a cubic Â O2a cubic (a cubic refers to the cubic structure), involving successive cooperative rotations of MnO 6 octahedra around the h111i crystallographic axis.The cell parameters of calcium manganite depend on the oxygen content that can be affected by the synthesis route in terms of ring temperature and cooling rate. 18,19The cell parameters determined from powder XRD are shown in Table 1, showing that the addition of Nb on the Mn site enlarges the cell parameters.
The reaction between zirconia and the cathode perovskite materials, especially those containing cobalt on the B-site, would cause the formation of insulating products, such as La 2 Zr 2 O 7 or SrZrO 3 that would block the transport of electrons/ ions between the electrode and electrolyte.The XRD patterns (Fig. 1) show no observable reaction aer 5 hour annealing in air in contact with YSZ at 950 C. No obvious variation of lattice parameter (Table 1) was observed.Thermodynamic calculation has predicted the formation of CaMn 2 O 4 for the CM-YSZ system at 1400 C, 20 which was not observed in our case due to the relatively low temperature.The compatibility of LSM is limited to 1200 C and can be improved by A-site deciency.Attempts have been made to prepare A-site decient Ca 0.95 MnO 3Àd and Ca 0.95 Mn 0.9 Nb 0.1 O 3Àd using the same method as for their stoichiometric counterparts, but CaMn 2 O 4 persisted as the impurity in both materials, even though the phase diagram 21 of CaO-Mn 2 O 3 indicated that 10% Asite decient was achievable.The A-site deciency of a perovskite was reported to be controlled by the bond energy of hB-Oi 22 and 5% A-site deciency for LSM was reported.

Chemical and structural transformations with temperature variation
The oxygen non-stoichiometries, d, were obtained by H 2 -reduction TGA.In order to analyze the TGA data, the initial assumption was made that the nal products of the reduction contained Mn in the +2 state and Nb in the +5 state. 15The oxygen non-stoichiometry, d, is listed in Table 1, and the ratio of Mn IV to Mn IV + Mn III is also calculated, assuming the charge neutrality of the perovskite.It can be seen that the oxygen content in CMN is higher than that of CM.A higher oxygen content in niobium doped CM was also reported by Kruth et al. 15 for the samples synthesized in air, due to the higher thermal stability with Nb doping during the high temperature synthesis.TGA under air and oxygen (Fig. 2) can provide information on structural and chemical changes occurring in the volume of CM and CMN with temperature variation.It can be seen that in oxygen atmosphere, CM also picks more weight than CMN to make the d value near zero aer calcination at 900 C for 1 hour.CMN is more stable against thermal treatment in air up to 900 C. The d values of CM and CMN change to 0.099 and 0.025 at 900 C in air, respectively.The changes of oxygen content caused by the valence variation of the transition metal were anticipated to be benecial to the electrochemical performance of the oxygen electrode. 23he Goldschmidt tolerant factor for perovskite structure, s, of the materials was calculated according to the equation: where, R A ¼ ionic radius of larger cation, R B ¼ ionic radius of smaller cation, R O ¼ ionic radius of oxygen (¼1.40 Å).
The R B for CM and CMN was calculated via the composition weighted average ionic radii of Mn IV , Mn III and Nb V .It can be seen that the addition of Nb into the lattice of CM increases the percentage of Mn III (Table 1) and decreases the tolerance factor thanks to the larger radii of Mn III (72 pm for low-spin) and Nb V (78 pm) than Mn IV (67 pm for low spin) under the similar oxygen content. 15The tolerance factors of both materials are ca.0.87, less than 1 for a cubic perovskite.On the one hand, Dabrowski et al. 25 found that the thermal stability of Sr 1ÀxÀy Ca x Ba y MnO 3 perovskites was governed by the magnitude of tolerance factor (s < 1) which can be adjusted by the oxygen content.Similarly, the stabilizing energy of a perovskite structure was found to be in a linear relationship to the tolerance factor (when s < 1). 26On the other hand, the substitution of a more electronegative Nb (electronegativity, c Nb ¼ 1.60) for Mn (c Mn ¼ 1.55) reduces the tendency to form oxygen vacancies. 27For example, Nb and Mo are reported to efficiently stabilize the cubic perovskite crystal structure of SrCoO 3Àd oxide, which is noted for both high oxide ionic and electronic conductivity at elevated temperature. 28,29A balance of the above two factors should strike a balance to control the thermal stability of CM and CMN.
The values of TEC in owing air are presented in Fig. 3.One can distinguish two segments with different TECs for both CM and CMN.The thermal expansion of CMN is more linear than CM in the whole temperature range.Both materials show quite similar TECs in the temperature range 25-750 C, but CM shows a much higher TEC between 750-900 C. A hysteresis of the shrinkage in the heating and cooling period was observed, and can be explained by the non-equilibrated release and recovery of oxygen of the bulk materials in air.Two TECs delimited at temperature ca.750 C were assumed for better tting of the expansion data.At temperatures below 750 C, both materials show similar TECs, ca. 13 ppm K À1 for heating and ca.11 ppm K À1 for cooling.On the contrary, CM shows much larger thermal expansion than CMN at temperatures above 750 C, reaching 21 ppm K À1 for heating and 25 ppm K À1 for cooling.The heavy doping of Nb on the B-site was reported to decrease the thermal expansion of LaCoO 3 , 30 but this is not obvious in our study unless at temperatures higher than 750 C. The additional expansion at higher temperatures can be a result of chemical expansion due to the change of Mn IV to the larger Mn III , similar to the phenomenon observed in Sr-doped lanthanum cobalt oxide. 31It should be noted that the thermal history of the sample is also very important to the TECs of the samples, as can be seen from the discrepancy between the heating-up and cooling-down process.More importantly, the thermal expansion in the cooling stage is closer to that of YSZ and more meaningful since the stress could arise from the strain in the cooling process aer the calcination of powder on the electrolyte.The in situ XRD patterns at temperatures up to 900 C in air were measured to study the crystal structure of CMN presented in Fig. 4 to provide a better equilibrium than dilatometry since very ne powders (as shown aerwards in this paper) were used for the determination of lattice parameters in this study.The in situ XRD patterns of CM and CMN were performed in static air with an environmental X-ray diffractometer with Mo target.The cell parameters of CMN at room temperature calculated from XRD with Mo target are a ¼ 5.3226(2) Å, b ¼ 7.5103(2) Å and c ¼ 5.3110(3) Å, and the volume of unit cell is 212.301(5)Å3 , which are quite similar to those from the XRD using a Cu K a1 X-ray diffractometer.The unit cell of the powder at room temperature before and aer high-energy milling was checked with Cu K a1 X-ray diffractometer, and no variation was observed.The uorescence of Mn-ion under characteristic X-ray of Cu target and Ka 2 of the Mo target would both affect the determination of cell parameters.It can be seen that CMN maintains the orthorhombic structure through the whole temperature range and the peaks shi toward the low angle direction along with increasing temperatures, indicating an expansion of the unit cells.The unit cell parameters (Fig. 5) of both materials during the heating stage were calculated by tting the peaks into an orthorhombic structure.The linear tting formula of unit cell parameters and parabolic tting parameters of cell volumes are inserted in the diagram and the thermal expansion from a-, b-and c-directions are listed in Table 2.The TECs calculated from V 1/3 (V ¼ volume of unit cells) are in correspondence to those from dilatometry in the heating up stage.Previous studies 17 on CM reported the existence of successive structural transitions from orthorhombic (Pnma) to tetragonal (I4/mcm) at 896 C and further to cubic (Pm 3m) at 913 C, but we observed the change from orthorhombic to cubic structure at temperatures higher than 800 C by analyzing the orthorhombicity of the structure, possibly due to the fast loss of oxygen due to the high surface area.It is obvious from the orthorhombicity that the addition of Nb clearly stabilizes the orthorhombic structure.A recent study has shown that chemical expansion is the result of two competing processes: 32 the lattice contraction primarily due to electrostatic interaction and the lattice expansion due to the cation radius change.The exceptionally large unit cell parameter for CM at 800 and 900 C could be the lattice expansion thanks to the higher concentration of Mn 3+ cation in the lattice due to the loss of oxygen.The thermal expansion is anisotropic and the thermal expansion in a-direction is much smaller than those in the b-and c-direction.Basically, the addition of 10% Nb in CM increases slightly the thermal expansion in the a-, b-and c-direction from the high temperature XRD, but wider temperature range for CMN could bring in more contribution from chemical expansion.The variation in temperature on CM between 25 C and 800 C showed a volumetric increase of 2.45%, 33 slightly smaller than the value of this study (3.26%).The high temperature XRD analysis of CaMn 0.98 Nb 0.02 O 3 in the temperature between 25 C and 900 C showed a volumetric increase of 4.40% (ref.27) and turned out to be a cubic structure at 900 C. The discrepancy in thermal expansion between different studies could be explained by a difference in the oxygen content in CM due to thermal history that can contribute to the chemical expansion at elevated temperatures. 31

Microstructure of the powders and oxygen electrode
In order to improve the sinterability of the powder at 950 C for better bonding between the oxygen electrode and electrolyte, the hand-ground powder was milled in a high-energy planetary milling machine for ner particles.The powder and milling media was mixed in isopropanol milled at a high speed of 650 rpm for 30 min.Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) were used to analyze the ne powder aer high energy milling and the results are shown in Fig. 6 and 7, respectively.It can be seen that the particle size of both materials is in the range between 10 nm to 2 mm and the CMN particles are slightly ner than those of CM.Amorphous phases are found in both CM and CMN.In particular, the former consists of small polycrystalline particles and covered with an amorphous layer while the latter composes of mostly a single crystal.The calculated d-spacings of the selected areas of CM and CMN are 0.257 nm and 0.271 nm respectively, as indicated in the Fig. 7, which could correspond to the (121) crystal planes.
The screen-printed layers (20-30 mm in thickness) composed of CM and CMN aer calcination at 950 C for two hours show good bonding to the YSZ electrolyte and similar grain size compared to the raw powder, as shown in Fig. 8.The grains lost their sharp edges in the sintering process and connected well to each other, which is benecial to the transport of electrons.

Electrochemical characterization
Electrochemical impedance spectroscopy was used to evaluate a symmetricalelectrode system (CM(N)|YSZ|CM(N)) to study the polarization resistance of the electrode at OCV in static air, as shown in Fig. 9.The Nyquist and Bode plots of the symmetrical electrode at 700 C are shown in Fig. 9(a).One arc can be distinguished for the CMN electrode, while two arcs for CM aer analyzing the Bode plots.The Arrhenius plots of the series resistance and polarization resistance are shown in Fig. 9(b) and (c).R s is obtained from the high-frequency intersection between the Nyquist plots and x-axis, and R p is calculated by the reduction of R s from the low frequency intersection between the Nyquist plots and x-axis.The log(R s ) shows a linear plot against the reciprocal of temperature (1000/T) and activation energy of 0.8 eV, which is slightly lower than the activation energy (>1.0 eV below 650 C) 34 of YSZ in the temperature below 700 C. The R s may compose of two parts: the ohmic resistance of YSZ electrolyte and CM or CMN   electrode.Even though the conductivity of CMN (125 S cm À1 at 700 C) is higher than that of CM (1-5 S cm À1 at 700 C), 12,19 the R s for both electrodes are similar, indicating that the ohmic loss from the electrode is negligible.The R p values for the CM and CMN electrodes are 3.40 and 5.53 U cm 2 , respectively and are quite close to that of LSM/YSZ oxygen electrode on YSZ electrolyte ($4 U cm 2 ) at 700 C. 5,35 The polarization resistance of CM or CMN on YSZ at 700 C is much smaller than that of SrMnO 3 or CM/Gd 0.1 Ce 0.9 O 2Àd (CGO) composite on CGO electrolyte at 700 C ($8 U cm 2 ) 11,14 and LSM electrode on YSZ ($10 U cm 2 at 800 C). 6 Porras-Vazquez et al. 11 found that the composite electrode CaMn 0.95 Si 0.05 O 3Àd /CGO showed a lower area-specic resistance (ASR) (0.35 Ucm 2 at 800 C) than CM/GDC (1.5 Ucm 2 at 800 C) and the increase of electric conductivity due to Si doping was thought to be the reason.With the benet of higher ionic conductivity, the addition of CGO can decrease the electronic conductivity of the electrode.It was reported that the doping of 10% Ta, 10% Nb or 5% Mo on B site stabilized the lowtemperature cubic structure of (La)SrCo(Fe)O 3Àd to avoid the negative effect of intermediate hexagonal structure for better performance, 28,29,[36][37][38] while in our case the addition of Nb stabilized the low temperature-orthorhombic structure that showed inferior performance than the undoped CM.The addition of YSZ into LSM as oxygen electrode was reported to enhance the performance of electrode by a factor of two at 800 C (ref.39) due to the enlargement of triple phase boundary (TPB), since LSM showed an ionic conductivity as low as 10 À7 S cm À1 . 9Two linear regions are implied in the Arrhenius plots and the activation energies in the temperature range 650-700 C are twice as large as those in 540-620 C. The changes in activation energy are ascribed to the shiing of rate-limiting step from bulk diffusion limiting to surface diffusion limiting as the temperature increases since the activation energy of the bulk diffusivity is normally half of the surface diffusivity.In order to study the properties of the electrodes under current load, a threeelectrode system with a reference electrode was used for the electrolysis measurement.The fuel electrode was Ni(O)-YSZ under N 2 -50% H 2 O-3% H 2 at a ow rate of 500 mL min À1 .Fig. 10 shows the typical impedance spectrum of the electrolysis cell with CMN as the oxygen electrode at OCV.The impedance spectrum between the reference and either anode or cathode allows one to determine the electrode loss from the nonohmic part of the spectrum.In a three-electrode system, the improper placement of the reference and working electrodes will give erroneous results.It is noteworthy that the ohmic resistances in both spectra are quite close, and almost one-half of the total ohmic resistance of the cell as indicated from the two-electrode testing, showing that the reference electrode is sampling the potential near the centre of the electrolyte.Furthermore, the characteristic frequencies, n*, for the fuel electrode spectra, 200 and 2 kHz, are different from that for the oxygen electrode, 80 Hz.For this cell, the fuel electrode and oxygen electrode impedances are 0. between the three electrode measurement and the previous symmetrical-cell measurement is caused by the additional activation of the oxygen electrode under 100 mA cm À2 cathodic current for 24 hours in the former case.It should be noted that the characteristic frequency of the CMN electrode is the same, 80 Hz, in both two electrode and three electrode systems.The electrodes can also be activated with anodic current since the same R p of 1.5 U cm 2 was observed if a 100 mA cm À2 current was passed through the symmetrical cell where a cathodic current for one electrode is anodic for the other.Similar polarization hysteresis has been observed in the LSM/ YSZ electrode, 5,42 in which polarization resistance decreased aer both cathodic and anodic current passage.
The IV curves of the electrolysis in the voltage range between À1.7 V to À0.82 V are shown in Fig. 11, where both IV curves show good linearity.The open circuit voltages (OCV) of both electrodes are 0.82 V, which is consistent with the  theoretical Nernst voltage calculated between air and N 2 ow containing 50% H 2 O-3% H 2 at 700 C. The maximum current at À1.7 V is 0.21 A cm 2 and 0.17 A cm 2 for the CMN and CM electrodes, respectively.The ASR calculated from the IV curve is 5.3 and 4.2 U cm 2 for the electrolyser with a CM and CMN oxygen electrode, respectively.The ASR value for the electrolyser with a CMN oxygen electrode are 20% smaller than that calculated from the impedance spectrum at OCV, 5.5 U cm 2 .Since the anode is kept as the same for both electrolysers, the difference in performance is attributed to the catalytic activity of the oxygen electrode for the oxidation of O 2À to O 2 .According to the impedance measurement, the ohmic loss from the 1 mm thick YSZ electrolyte contributes a large portion of the total loss at 700 C.However, this conguration does not affect the comparison between the two materials as oxygen electrodes for oxygen oxidation.The Nyquist and Bode plots of the CM electrode are shown in Fig. 12(a).The characteristic frequencies for CM increase to a higher frequency aer activation under 100 mA cm À2 cathodic current, which could be attributed to the change of surface and capacitance.The polarization resistance of the oxygen electrode under bias was measured using impedance and presented in Fig. 12(b).However, CM presents a polarization resistance of 0.059 U cm 2 under À0.4 V bias as the cathode for fuel cell operation while CMN gives a polarization resistance of 0.081 U cm 2 under 0.4 V bias as the anode for the electrolysis process.Considering the R s is higher than R p for both electrodes at all biases, the maximum actual voltage loss on the electrode under a bias of 0.4 V is lower than 0.2 V, which is quite a reasonable loss for the oxygen electrode in either fuel cell or electrolyser modes.The reversible decrease in impedance upon cathodic polarization of LSM-based electrodes has been observed by several groups, and the mechanism was not denitely clear, 43,44 but the reduction of LSM surface could be involved in the activation process.Similarly, the loss of oxygen on the surface of CM during the reduction process could result in the formation of vacancies through eqn (2), 45 which are benecial to fast transport of the oxygen ion in the electrode.Here, the Kroger-Vink notations are used. 46The oxygen vacancies could also be ordered to be immobile and the highest conductivity for CM was achieved at d ¼ 0.08 where no oxygen vacancy was observed. 47,48Under anodic current, the decrease in the non-stoichiometry due to the absorption of O 2 means the loss of oxygen vacancies, and explains the resultant decrease of performance in the bias range of 0.2-0.4V. Aguadero et al. 29 stipulated that the performance increase of SrCo 1Àx Mo x O 3 oxygen electrode under anodic current was due to the increase of p-type carriers that improves the electrocatalytic properties.This may help to explain the decrease of performance of CM a typical n-type oxide 48 under anodic current.On the other hand, because CMN is more difficult to be reduced as demonstrated in the TGA curves, there is only a slight improvement in the performance under cathodic current due to the negligible increase of oxygen vacancies.CMN can be more stable under anodic current that preserves the oxygen vacancy for the transport of oxygen ions.Moreover, an oxygen-excess CMN (d ¼ À0.1) was synthesized with high oxygen pressure, 15 and it was not very clear if the interstitial oxygen could also be a route of oxygen transport. 47,49nclusion CM and CMN were examined as oxygen electrodes for SOEs and SOFCs.The addition of 10 mol% Nb on the B site of perovskite improved the thermal stability of CM in air and oxygen up to 900 C. Both materials showed a thermal expansion of 10.8-10.9ppm K À1 , close to that of YSZ ($11 ppm K À1 ).At 700 C, CM as a cathode for SOFCs could achieve a polarization resistance less than 0.1 U cm 2 , but CMN showed superior performance (R p < 0.1 U cm 2 at 0.4 V bias) as an anode for SOECs.The performance of the electrode can be further improved by mixing with ionic conductors to make a composite electrode.A possible exploration of the materials with a Nb content less than 10 mol% doping on Mn site would lead to a better oxygen electrode performance in both SOFC and SOE mode.

Fig. 1
Fig.1XRD patterns of CM and CMN with YSZ after calcination at 950 C for 5 hours.The peaks indexed with "Z" belong to YSZ and the rest to perovskites.

Fig. 2
Fig. 2 TGA curves CM (open circles) and CMN (open squares) in air and O 2 .The heating or cooling direction is indicated with the arrow.The ramp rate is 10 C min À1 .

Fig. 3
Fig. 3 Dilatometry of the CM and CMN samples in the temperature range between 150 and 900 C. The ramp rate for the heating and cooling was 3 C min À1 and the samples dwelled in flowing air at 900 C for 1 hour before cooling down.

Fig. 4
Fig. 4 High temperature XRD spectra of CMN from 25 to 900 C in static air.The insert is the magnified region in between 14-20 .The temperature ( C) is indicated beside the graph.A standard powder diffraction file (pdf) of CM is provided to show the rough position of peaks.

Fig. 5
Fig. 5 Temperature dependence of lattice parameters for CM (a) and CMN (b) and their cell volume dependence on temperature (c).Error bars are within the symbols.(d) Shows the orthorhombicity of CM and CMN in terms of a/c and O2a/c.The linear fitting of the unit cell in selected temperature ranges is indicated in the respective graphs of (a) and (b) and the parabolic simulation of cell volume with temperature is indicated in (c).The unit cell parameter (a cubic ) and volume (V cubic ) of the cubic phase (Pm 3m) for CM at 800 and 900 C is scaled by O2 and 4, respectively, for better comparison.

Fig. 6
Fig. 6 SEM images of CM (a) and CMN (b) after milling with high-energy planetary milling.

Fig. 8
Fig. 8 SEM images of post-test CM (a and c) and CMN (b and d) after calcination at 950 C for 2 hours in air and testing at 700 C for symmetrical cells.
Fig. 9 (a) The impedance spectra (Nyquist plots and bode plots) of CM and CMN at 700 C in static air.Arrhenius plots of the R s (b) and R p (c) at OCV before activation for the symmetrical cells in the temperature range between 550 to 700 C. The activation energies of R s and R p are indicated in the respective diagrams.

Fig. 10
Fig. 10 Impedance with three-electrode system for the CMN oxygen electrode, Ni/YSZ hydrogen electrode and the whole electrolyser.

Fig. 11 IV
Fig. 11 IV curves of the electrolyser with CM and CMN oxygen electrode after activation for 24 hours under cathodic current 100 mA cm À2 .The steam electrode is Ni/YSZ in N 2 -50% H 2 O-3% H 2 at a flow rate of 500 mL min À1 .

Fig. 12
Fig. 12 Nyquist and Bode plots (a) of the CM and CMN cathodes at 700 C in static air at OCV immediately after the activation at 100 mA cm À2 cathodic current for 24 hours.(b) is the R p measured under bias for both electrodes with three-electrode system.The counter electrode is a Ni/YSZ electrode in N 2 -50% H 2 O-3% H 2 at a flow rate of 500 mL min À1 .

Table 1
Cell parameters (in Å) and volume (Å 3 ) of CM and CMN with symmetry of Pnma, oxygen nonstoichiometry, (d) from TGA measurement and the Goldschmidt tolerance factors, s a

Table 2
Thermal expansion values of CM and CMN from high temperature XRD in selected temperature ranges.The unit of thermal expansion is ppm K À1 Open Access Article.Published on 08 April 2015.Downloaded on 11/01/2018 18:19:27.This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.