Amir Reza Hanifi
University of Alberta
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Publication
Featured researches published by Amir Reza Hanifi.
Journal of Materials Chemistry | 2014
M. A. Laguna-Bercero; Amir Reza Hanifi; Hernán Monzón; Joshua Cunningham; Thomas H. Etsell; Partha Sarkar
Nd2NiO4+δ infiltrated into porous yttria stabilized zirconia (YSZ) is proposed in this work as a cathode for solid oxide fuel cells (SOFCs). In order to obtain nickelate single phase, calcination times and temperatures of the salt precursors are studied. Anode supported microtubular cells using this cathode are fabricated and characterized, showing power densities of about 0.76 W cm−2 at 800 °C and a voltage as high as 0.8 V. No degradation is detected after 24 hours under current load, assuring reasonable stability of the cell. Preliminary solid oxide electrolysis cell (SOEC) results show slightly better performances in comparison with SOFC operation. It is believed that infiltration of nickelate salt precursors followed by calcination proposed in this work avoids high temperature sintering of the nickelate phase with the electrolyte and as a consequence, prevents their reaction. For this reason, infiltrated nickelates are very attractive for their use as intermediate temperature (IT) SOFC cathodes.
Materials Science Forum | 2007
Amir Reza Hanifi; Annaik Genson; Michael J. Pomeroy; Stuart Hampshire
Ca-Sialon glasses have been known for some time [1] and they are effectively calciumalumino- silicate glasses containing nitrogen which improves their mechanical properties. Calciumalumino- silicate glasses containing fluorine are known to have useful characteristics as potential bioactive materials [2]. Therefore, the combination of both nitrogen and fluorine additions to these glasses may give useful bioglasses with enhanced mechanical stability.Addition of fluorine to oxynitride glasses was not reported previously and this paper gives the first report of the glass forming regions (and evaluation of some properties) in the Ca-Si-Al-O-N-F system. Within the previously defined [1] glass forming region in the Ca-Si-Al-O-N system, homogeneous, dense glasses are formed. Addition of fluorine extends the glass forming region but also increases the reactivity of the glass melts. One major problem is fluorine loss as SiF4, but also loss of nitrogen, which affects the final composition and results in porous samples. To suppress the fluorine loss and CaF2 precipitation, consideration of the ratio of cations to fluorine and the coordination number of Al atoms is important. Discussion of the role of cations in these oxyfluoronitride glasses is presented.
Scientific Reports | 2016
Amir Reza Hanifi; M. A. Laguna-Bercero; Navjot Kaur Sandhu; Thomas H. Etsell; Partha Sarkar
In this study, the effects of calcination and milling of 8YSZ (8 mol% yttria stabilized zirconia) used in the nickel-YSZ anode on the performance of anode supported tubular fuel cells were investigated. For this purpose, two different types of cells were prepared based on a Ni-YSZ/YSZ/Nd2NiO4+δ-YSZ configuration. For the anode preparation, a suspension was prepared by mixing NiO and YSZ in a ratio of 65:35 wt% (Ni:YSZ 50:50 vol.%) with 30 vol.% graphite as the pore former. As received Tosoh YSZ or its calcined form (heated at 1500 °C for 3 hours) was used in the anode support as the YSZ source. Electrochemical results showed that optimization of the fuel electrode microstructure is essential for the optimal distribution of gas within the support of the cell, especially under electrolysis operation where the performance for an optimized cell (calcined YSZ) was enhanced by a factor of two. In comparison with a standard cell (containing as received YSZ), at 1.5 V and 800 °C the measured current density was −1380 mA cm−2 and −690 mA cm−2 for the cells containing calcined and as received YSZ, respectively. The present study suggests that the anode porosity for improved cell performance under SOEC is more critical than SOFC mode due to more complex gas diffusion under electrolysis mode where large amount of steam needs to be transfered into the cell.
Key Engineering Materials | 2007
Stuart Hampshire; Amir Reza Hanifi; Annaik Genson; Michael J. Pomeroy
Oxynitride glasses are effectively alumino-silicate glasses in which nitrogen substitutes for oxygen in the glass network, resulting in increases in glass transition and softening temperatures, viscosities (by two to three orders of magnitude), elastic moduli and microhardness. Calcium alumino-silicate glasses containing fluorine are known to have useful characteristics as potential bioactive materials. Therefore, the combination of both nitrogen and fluorine additions to these glasses may give useful bioglasses with enhanced mechanical stability. This paper gives a review of oxynitride glasses and reports glass formation and evaluation of glass properties in the Ca-Si-Al-O-N-F system. Within the previously defined glass forming region in the Ca-Si-Al-O-N system, homogeneous, dense glasses are formed. However, addition of fluorine affects glass formation and reactivity of the glass melts and can lead to fluorine loss as SiF4, but also nitrogen loss, and cause bubble formation. At high fluorine and high Ca contents under conditions when Ca- F bonding is favoured, CaF2 crystals precipitate in the glass. It was found that fluorine expands the glass forming region of Ca-Sialon system and facilitates the solution of nitrogen into the melt.
Materials Science Forum | 2007
Annaik Genson; Amir Reza Hanifi; A.Vande Put; Michael J. Pomeroy; Stuart Hampshire
The preparation of bulk glasses in Ca-Si-Al-O-N-F system with the composition in equivalent % of 28e/oCa:56e/oSi:16e/oAl:100-X-Ye/oO:Xe/oF:Ye/oN are reported. The glass formation behaviour and properties of this new range of glasses are examined in detail. Fluorine decreases the glass transition temperature, the density and the mechanical properties of the glasses while nitrogen increases them. Therefore, it appears that fluorine acts as a network modifier while, on the contrary, nitrogen acts as a network former even in presence of fluorine.
Journal of Power Sources | 2012
Adrien Vincent; Amir Reza Hanifi; Jing-Li Luo; Karl T. Chuang; Alan R. Sanger; Thomas H. Etsell; Partha Sarkar
Journal of The Electrochemical Society | 2011
Alireza Torabi; Amir Reza Hanifi; Thomas H. Etsell; Partha Sarkar
International Journal of Hydrogen Energy | 2014
Amir Reza Hanifi; M. A. Laguna-Bercero; Thomas H. Etsell; Partha Sarkar
Solid State Ionics | 2011
Amir Reza Hanifi; Alireza Torabi; Thomas H. Etsell; Luis Yamarte; Partha Sarkar
Journal of the American Ceramic Society | 2009
Amir Reza Hanifi; Annaı̈k Genson; Michael J. Pomeroy; Stuart Hampshire