Journal of Materials Science and Chemical Engineering
Vol.06 No.06(2018), Article ID:85505,9 pages

Proton Conductivity of Ni, Y Co-Doped BaZrO3

Hiroya Morishita1, Yumiko Ikebe2, Eriko Ban2*

1Department of Materials Science and Engineering, Meijo University, Nagoya, Japan

2Department of Applied Chemistry, Meijo University, Nagoya, Japan

Copyright © 2018 by authors and Scientific Research Publishing Inc.

This work is licensed under the Creative Commons Attribution International License (CC BY 4.0).

Received: May 21, 2018; Accepted: June 23, 2018; Published: June 26, 2018


Dense sintered bodies of proton conducting BaZrO3 (BZ) and Y-doped BaZrO3 (BZ-Y) were obtained at 1600˚C for a short sintering time of 5 hours, by the addition of NiO as a sintering promotion agent. The relative density and grain growth of samples, Ni-doped BaZrO3 (BZ-N) and Ni, Y co-doped BaZrO3 (BZ-NY), were increased with increasing Ni addition. The sinterability of BZ-NY was greatly improved just to add only 0.6 mol% Ni and the relative density of this sample was more than 98%, in contrast to that of 60% at most for BZ-Y without Ni addition. Electrical conductivity of BZ-NY added Ni 1.0 mol%, BaZr0.91Ni0.01Y0.08O3-α, was more than 103 S∙cm2 at 900˚C in a wet 1% hydrogen atmosphere, which value was 10 times higher than that of BZ-Y. In addition, the kind of electrical conduction carrier and an ionic transport number were also examined by employing various concentration cells. It was found that the proton conduction was dominant for both BZ-N and BZ-NY samples, although BZ-NY showed scarcely oxygen-ion conduction approximately 10% in a high temperature range higher than 800˚C. From these results, as mall amount of Ni addition found to be effective for improvement of both the sinterability and the electrical conductivity.


Proton Conducting Oxide, Barium Zirconate, Ni, Y Co-Doping, Electrical Conductivity, Ionic Transport Number

1. Introduction

The electrochemical device employing proton conducting perovskite-type oxide has a great potential for practical applications, such as a large scale fuel cell and hydrogen sensor etc. [1] . Among these proton conducting ceramics, barium cerate (BaCeO3; BC) and barium zirconate (BaZrO3; BZ) are the well-known materials [1] [2] . BZO partially substituted by low valence cations has been paid great attention to because of the superior mechanical strength and good chemical stability [3] [4] . However, the BZ doped with additive is very difficult to sinter, that is, high temperature more than 1700˚C is necessary to obtain a high-density sample. BZ sample without sintering additives shows low conductivity for grain-boundary resistivity even though a long time heat treatment at high temperature was carried out [1] [5] [6] [7] . In order to overcome these problems, it has been recognized that addition of small amount of transition metal (Co, Ni, Cu, Zn, etc.) as a sintering promotion agent is effective on improvement of sinterability [8] [9] [10] [11] [12] . Because Ni is used for the anode electrode material of a fuel cell [13] [14] , further consideration is required to obtain the high performance fuel cell using BZ and BZ-Y electrolyte. Therefore, in other word, it is connected for elucidation of the influence of interfacial reaction between the electrolyte and the electrode, diffusion of Ni and the coefficient of thermal expansion. It is also very important for the fundamental research and application to understand the roll of Ni additive mechanism.

In this study, the sinterability and the electrical properties of BaZr1-x(Ni, Y)xO3-α co-doped with mixture of Ni and Y are investigated. Their proton conductivities are also examined.

2. Experimental Procedure

The powder for bulk samples was synthesized by an ordinary solid state reaction method. Two kinds of sample with NiO additive representing the chemical formula of BaZr1-aNiaO3-α (BZ-N) and BaZr0.92-bNibY0.08O3-α (BZ-NY) were prepared by using commercially available BaCO3, ZrO2, Y2O3 and NiO as starting reagents. These reagents were mixed with an organic solvent by using a planetary-motion ball-milling machine. After drying at 60˚C for 30 min, the mixed powders were calcined at 1200˚C for 5 h in air. Two times of ball-milling operation was repeated to make the size of the particle smaller. By using the uniaxial pressing and cold isostatic pressing (CIP), thus prepared calcined powders were molded into a pellet of 20 mm in diameter by adding molding pressure of 200 MPa for 2 min. The green pellets were sintered at 1600˚C for 5 h in air at a heating rate of 200˚C/h from room temperature to 1300˚C and 50˚C/h to 1600˚C/h and cooling rate of 50˚C/h from 1600˚C to 1400˚C/h and 200˚C/h to room temperature. Differential thermal analysis (DTA), differential scanning calorimetry (DSC) and thermomechanical analysis (TMA) was used to study transition and melting behavior of samples at a heating and cooling rate of 10˚C/min.

After heat treatment, the crystal structure of sample was analyzed using X-ray diffractometer (XRD). The microstructural observation and the chemical composition were examined by a scanning electron microscope (SEM) and an energy dispersive X-ray analyser (EDXA). The relative density measurement by the Archimedes method was performed as evaluation of sinterability. For the measurements of electrical properties, porous platinum mesh was attached on both sides of pellet using Pt paste as electrodes. Electrical conductivities were measured at temperature range of 500˚C - 900˚C in wet 1% H2 + Ar atmosphere by complex impedance method. Furthermore, in order to investigate the proton contribution to conduction, an electromotive force (EMF) was also measured at temperature range of 500˚C - 900˚C by using some kind of gas concentration cell, such as a hydrogen gas concertation cell and a water vapor concentration cell.

3. Results and Discussion

3.1. Sinterability and Microstructure

After sintering, we examined the crystal phases of the samples by XRD analysis. The diffraction patterns indicated that all samples doped with Ni lower than 0.05 mol showed highly crystalline BaZrO3 phase, but the reflection peaks of secondary NiO phase were also detected in samples which added Ni more than amolar ratio of 0.05. From SEM observation and EDX analysis, NiO precipitates and the related Ni-rich regions were confirmed on surface of these samples. Therefore, samples less than Ni adding 1.0 mol% are subsequently investigated.

Figure 1 shows the relationships between the relative density of BZ-N and BZ-NY and Ni contents. Both samples sintered at 1600˚C for 5 h exhibit the tendency that the relative density of samples increases with increasing Ni-doping level. The relative density of BZ-NY doped with Ni higher than a molar ratio of 0.006 remarkably improves, contrast to that of BZ-NY without Ni is 60% at most. BZ-NY samples doped with Ni higher than a molar ratio of 0.008 showed the relative density exceed 99%. The Ni addition higher than a molar ratio of 0.006 is found to be effective to obtain a high-density sintered body for BZ-N and BZ-NY.

In the case of BZ-NY heat-treated at rather low temperature, the BZ-NY with Ni 0.006 mol showed dense structure even when at low sintering temperature around 1300˚C. Thermal analysis using TG and DSC was performed to investigate the thermal behaviour. The powdery sample was BaCO3 and NiO which were mixed by the molar ratio of 1:1. TG and DSC profiles are shown in Figure 2. TG curve exhibits weight loss of 15.6% which is shown at temperature range from 800˚C to around 950˚C due to decomposition of BaCO3. The other hands, DSC signal reveals some thermal events, the main of which, at around 1130˚C, is distinct endothermic peak. It is thought that this temperature corresponds to the partial melting by a reaction between Ba and Ni.In spite of the fact that both the volume shrinkage and a melting feature were confirmed in the sample which sintered at 1200˚C, these features could not be seen in the 1100˚C heat-treated sample. It is assumed that a generation of a reaction product such as BaNiOx proceeds continually at higher temperature. The consequence means that the change of solid phase reaction to liquid phase reaction occurred at even low temperature range of between 1100˚C and 1200˚C by a Ni addition, and then dense structure was formed.

Figure 1. Relative density of BZ-N and BZ-NY pellets sintered at 1600˚C for 5 h.

Figure 2. TG and DSC profiles for a mixed powder of BaCO3 and NiO.

Figure 3 shows the typical microstructure of fracture surface for BZ-N and BZ-NY. In the case of BZ-N shown in upper row, the microstructure drastically changes by Ni addition even though the small amount of Ni. Although Ni-free sample shows the microstructure constructed with smaller grains less than 1 μm, the crystal grain grown is obviously promoted in the Ni-doped samples. Similar consequence is reported in other works, which shows that small grain size and the densification of Y-doped BZO treated in an ordinary sintering condition [15] . It seems that the sintering is accelerated due to producing the partially melted liquid phase because melt point is below 1600˚C for composition of Ba and Ni. In Ref. [16] , it has been reported that NiO helps reducing sintering time and temperature which mitigates the extent of unwanted reactions. Bozza et al. have reported that Ni inclusion strongly enhanced densification and grain growth process [12] . Our experimental result on the sinterability shows a similar tendency and accords with other reports.

Although we did not show it in the figure, the following experimental result

Figure 3. SEM images of the fracture surface for pellets sintered at 1600˚C for 5h. Upper row: BaZr1-aNiaO3-α (a = 0, 0.005 and 0.01), Lower row: BaZr0.92-bNibY0.08O3-α (b = 0, 0.004 and 0.01).

about dispersibility and solid solubility limit of Ni was also acquired. SEM observation showed that NiO particles were dispersed in the grain boundary for BZ-N when the Ni doping level was higher than a molar ratio of 0.01. Furthermore, due to the detection of impurities phases of XRD analysis for this sample, we derived that the solubility limit of Ni to BZ sample was under 0.01 mol. Same results have been reported that a small amount of Ni addition around 0.004mol into BaCe0.9Y0.1O3-α is effective on the improvement of sinterability [10] .

3.2. Electrical Properties

Effect of Ni addition on the electrical conductivity of BZ-N and BZ-NY was investigated. Figure 4 shows the total conductivities formed Arrhenius plot for BZ-N and BZ-NY samples measured in wet 1% H2 + Ar atmosphere. Both sample showed the increased the conductivity with increasing Ni doping concentration and measurement temperature. Although grain size of BZ-NY samples are smaller than one of BZ-N samples as shown in Figure 3, the conductivities of BZ-NY samples are high. In addition, we confirmed in calculation that the activation energy of this sample is small. Similar consequence, the improvement of the conductivity for BZO by Y doping, has reported [17] . In this present work, the total conductivities of these samples increase with increasing Ni-doping level when the Y and Ni were co-doped. It seems that the grain boundary resistance of these samples tends to reduce with the increase in Ni content from Cole-Cole plot by complex impedance measurement. Because the grain-boundary resistivity is known to adversely affect electric conductivity of BZO [4] [7] , therefore we assume that improvement of sinterability by Ni-doping leads to the enhancement of conductivity.

These solid electrolytes under wet hydrogen atmosphere have the possibility of candidate of the electrical conducting carrier that H+, O2−, h+, e and metal cations of the constituent elements, such as Ba2+, Zr4+, Y3+ and Ni2+ contribute to conduction.

Figure 4. Arrhenius plots of total conductivities for the BaZr1-aNiaO3-α and BaZr0.92-bNibY0.08O3-α.

To investigate what kind of electrical conductive species affects electrical conductivity, we measured EMF of hydrogen concentration cell. Figure 5 shows EMF of hydrogen concentration cell by using BaZr0.99Ni0.01O3-α and BaZr0.912Ni0.008Y0.08O3-α. The theoretical electromotive force is shown in the figure with a broken line. Both samples obtain EMF of equivalent to the theoretical value calculated from Nernst’s equation at from 500 to 900°C. This indicates that ion (proton and oxygen ion) is major conductive species. Therefore, we consider that there is little conduction with h+ and e in both samples.

To estimate proton conduction regarding ion conduction in samples, we calculated oxygen ion transport number (to) by measuring EMF of water vapour concentration cell. Proton transport number (tp) in samples is obtained from the formula (1) shown below.

tp = 100 − to (1)

Figure 6 shows relationships between proton transport number and operating temperature for BaZr0.99Ni0.01O3-α and BaZr0.912Ni0.008Y0.08O3-α pellets. For comparison, the proton transport number of BaCe0.95Y0.05O3-α measured in same condition are also shown with explanatory note of the black circle. BZ-N samples have over 95% of proton transport number regardless of operating temperature. Proton transport number of BZ-NY samples is the same as BZ-N samples. When operating temperature exceeds 700˚C, proton transport number of BZ-NY samples reduces and samples have a little contribution of oxygen ion conduction. The contribution of the oxygen ion transference number of these BZ-N and BZ-NY samples is small whereas the ratio of oxygen ion transference number for BaCe0.95Y0.05O3-α is increased up to 27% with increasing the temperature. It was confirmed that the proton conduction is dominant for the BZ-N and BZ-NY.

Figure 5. EMF of the hydrogen concentration cell for BaZr0.99Ni0.01O3-α and BaZr0.912Ni0.008Y0.08O3-α. Theoretical EMF was shown by broken lines.

Figure 6. Proton transport number measured at various temperature by water vapour concentration cell for BaZr0.99Ni0.01O3-α and BaZr0.912Ni0.008Y0.08O3-α.

4. Conclusions

The relative density and grain growth of BZ-N and BZ-NY samples were increased with increasing Ni doping. Ni addition leaded both the decrease of the grain boundary resistance and high conductivity. The relative density hither than 99% was obtained in the samples with Ni-doping in amount of more than 0.008 mol, even when the sample treated at 1600˚C for rather short time sintering. On the other hand, NiO precipitation was observed in BZ-N doped with Ni 0.01 molar ratio. The solid solubility limit of Ni is assumed to be lower than 0.01 molar ratio.

The EMF of both BZ-N and BZ-NY samples accorded with the theoretical value regardless of measurement temperature, ion conduction of proton and oxygen ion is dominant to all that in wet hydrogen atmosphere. From the measurement result of hydrogen and water vapor concentration cell, BZ-N electrolyte indicates the proton transport number higher than 95%. It is suggested that the proton conduction is dominant for both BZ-N and BZ-NY samples, though BZ-NY has a few oxygen conduction at high temperature range higher than 800˚C.

Cite this paper

Morishita, H., Ikebe, Y. and Ban, E. (2018) Proton Conductivity of Ni, Y Co-Doped BaZrO3. Journal of Materials Science and Chemical Engineering, 6, 19-27.


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