Transition Metal D$ LaGaO3 Perovskite Fast Oxide Ion Conductor and Intermediate Temperature Solid Oxide Fuel Cell

1999 ◽  
Vol 575 ◽  
Author(s):  
Tatsumi Ishihara ◽  
Takaaki Shibayama ◽  
Miho Honda ◽  
Hiroyasu Nishiguchi ◽  
Yusaku Takita

ABSTRACTDoping transition metal cation is known to enhance the electric conduction of solid electrolytes, however, the ionic conduction can be improved by doping the small amount of transition metal, in particular, doping Co is effective for improving the oxide ion conductivity. In this investigation, oxide ion conductivity of LaGaO3 based oxide doped with Co were investigated in detail. It was found that LaGaO3 doped with Co for Ga site (LSGMC) show a notable oxide ion conductivity over a wide range of oxygen partial pressures, although a hole conduction was appeared by addition of excess amount of Co. Considering the electrical conductivity and transport number of oxide ion, the optimized composition of LSGMC seems to be existed at La0.8.Sr0.2, Ga0.8,.Mg0.115 CO0.085O3. Power generation characteristics of fuel cells was greatly improved by using LSGMC for electrolyte and extremely large power density can be obtained on both H2- O2 and H2-air cells. In particular, the maximum power density was attained to a value of 1.53 and 0.50 W/cm2 at 1073 and 873 K, respectively, on H2–O2 cell when the thickness of electrolyte was 0.18 mm. Furthermore, almost similar large power density was attained when air was used as oxidant. The high power density of cell demonstrated in this study suggests that the operating temperature of SOFC can be decreased by using LSGMC for electrolyte.

2005 ◽  
Vol 242-244 ◽  
pp. 159-168 ◽  
Author(s):  
Katsuyoshi Kakinuma ◽  
Hiroshi Yamamura ◽  
Tooru Atake

We have discovered a high oxide ion conductor within the perovskite-type (Ba1-x-ySrxLay)InO2.5+y/2 solid-solution system. The system was derived from brownmillerite-type Ba2In2O5, which possessed a ordered oxide ion vacancies. When we doped La3+ into the Ba site, the vacancy changed to a disordered state. The oxide ion conductivity increased with the amount of doped La3+, reaching a maximum value of 0.12 (S/cm) at 800 oC in (Ba0.3Sr0.2La0.5)InO2.75, a level exceeding that of yttria-stabilized zirconia. The oxide ion conductivity of this system was strongly dependent on the unit cell free volume, which appears to be the key parameter governing oxide ion mobility.


RSC Advances ◽  
2015 ◽  
Vol 5 (88) ◽  
pp. 71890-71895 ◽  
Author(s):  
Hongqiang Ma ◽  
Kun Lin ◽  
Longlong Fan ◽  
Yangchun Rong ◽  
Jun Chen ◽  
...  

Tetragonal tungsten bronze compound, BaBiNb5O15, is found to be a new type of oxide ion conductor with a total electrical conductivity of 3 × 10−4 S cm−1 at 600 °C.


2017 ◽  
Vol 56 (12) ◽  
pp. 6897-6905 ◽  
Author(s):  
Jungu Xu ◽  
Jiehua Wang ◽  
Xin Tang ◽  
Xiaojun Kuang ◽  
Matthew J. Rosseinsky

2019 ◽  
Vol 7 (44) ◽  
pp. 25503-25510 ◽  
Author(s):  
Matthew S. Chambers ◽  
Kirstie S. McCombie ◽  
Josie E. Auckett ◽  
Abbie C. McLaughlin ◽  
John T. S. Irvine ◽  
...  

Ba3NbMoO8.5 has recently been demonstrated to exhibit competitive oxide ion conductivity and to be stable under reducing conditions, making it an excellent potential electrolyte for solid oxide fuel cells.


2019 ◽  
Author(s):  
Jian Li ◽  
Fengjuan Pan ◽  
Shipeng Geng ◽  
Cong Lin ◽  
Mathieu Allix ◽  
...  

<p>CeNbO<sub>4+δ</sub>, a family of oxygen hyperstoichiometry materials with varying oxygen contents (CeNbO<sub>4</sub>, CeNbO<sub>4.08</sub>, CeNbO<sub>4.25</sub>, CeNbO<sub>4.33</sub>) and showing mixed electronic and oxide ionic conduction, have been known for four decades. However, the oxide ionic transport mechanism has remained unclear due to the unknown atomic superstructures of CeNbO<sub>4.08</sub> and CeNbO<sub>4.33</sub>. Here, we determinate the complex superstructures of CeNbO<sub>4.08 </sub>(89 unique atoms), <a>CeNbO<sub>4.25 </sub>(75 unique atoms) and CeNbO<sub>4.33</sub> (19 unique atoms) by using recently developed continuous rotation electron diffraction (cRED) technique from nano single crystals. </a><a>The Ce cationic size contraction upon oxidation in CeNbO<sub>4+δ</sub> allows not only excess oxygen incorporation into the CeNbO<sub>4</sub> host lattice at the interstitial site within the Ce cation chains (referred to as O<sub>i</sub>), but also relaxation of the<sub> </sub>NbO<sub>n</sub> polyhedra in CeNbO<sub>4.08</sub>, CeNbO<sub>4.25</sub>, CeNbO<sub>4.33</sub> being bridged through mixed corner/edge-sharing in 3-dimentional directions. </a>Two kinds of oxide ion migration events are identified in CeNbO<sub>4.08</sub> and CeNbO<sub>4.25</sub> phases by molecular dynamic simulations, which form long-rang 3-dimensional migration pathway through the interstitial sites O<sub>i</sub> via a synergic-cooperation knock-on mechanism involving continuous breaking and reformation of Nb<sub>2</sub>O<sub>9</sub> units. However, the excess oxygen in the CeNbO<sub>4.33</sub> phase hardly migrates because of ordered distribution of high-concentration excess oxide ions. The relationship between the structure and oxide ion migration for the whole series of CeNbO<sub>4+</sub><sub>d</sub> compounds elucidated here provides a direction for the performance optimization of these compounds and the development of oxygen hyperstoichiometric materials for wide variety of applications.</p>


2020 ◽  
Vol 8 (47) ◽  
pp. 25120-25130
Author(s):  
Fan Yang ◽  
Julian S. Dean ◽  
Qiaodan Hu ◽  
Patrick Wu ◽  
Emilio Pradal-Velázquez ◽  
...  

Low levels of acceptor-type dopants can introduce appreciable levels of oxide-ion conductivity into NB0.51T due to a synergistic effect from defect chemistry and ceramic microstructure.


2019 ◽  
Author(s):  
Jian Li ◽  
Fengjuan Pan ◽  
Shipeng Geng ◽  
Cong Lin ◽  
Mathieu Allix ◽  
...  

<p>CeNbO<sub>4+δ</sub>, a family of oxygen hyperstoichiometry materials with varying oxygen contents (CeNbO<sub>4</sub>, CeNbO<sub>4.08</sub>, CeNbO<sub>4.25</sub>, CeNbO<sub>4.33</sub>) and showing mixed electronic and oxide ionic conduction, have been known for four decades. However, the oxide ionic transport mechanism has remained unclear due to the unknown atomic superstructures of CeNbO<sub>4.08</sub> and CeNbO<sub>4.33</sub>. Here, we determinate the complex superstructures of CeNbO<sub>4.08 </sub>(89 unique atoms), <a>CeNbO<sub>4.25 </sub>(75 unique atoms) and CeNbO<sub>4.33</sub> (19 unique atoms) by using recently developed continuous rotation electron diffraction (cRED) technique from nano single crystals. </a><a>The Ce cationic size contraction upon oxidation in CeNbO<sub>4+δ</sub> allows not only excess oxygen incorporation into the CeNbO<sub>4</sub> host lattice at the interstitial site within the Ce cation chains (referred to as O<sub>i</sub>), but also relaxation of the<sub> </sub>NbO<sub>n</sub> polyhedra in CeNbO<sub>4.08</sub>, CeNbO<sub>4.25</sub>, CeNbO<sub>4.33</sub> being bridged through mixed corner/edge-sharing in 3-dimentional directions. </a>Two kinds of oxide ion migration events are identified in CeNbO<sub>4.08</sub> and CeNbO<sub>4.25</sub> phases by molecular dynamic simulations, which form long-rang 3-dimensional migration pathway through the interstitial sites O<sub>i</sub> via a synergic-cooperation knock-on mechanism involving continuous breaking and reformation of Nb<sub>2</sub>O<sub>9</sub> units. However, the excess oxygen in the CeNbO<sub>4.33</sub> phase hardly migrates because of ordered distribution of high-concentration excess oxide ions. The relationship between the structure and oxide ion migration for the whole series of CeNbO<sub>4+</sub><sub>d</sub> compounds elucidated here provides a direction for the performance optimization of these compounds and the development of oxygen hyperstoichiometric materials for wide variety of applications.</p>


2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Jian Li ◽  
Fengjuan Pan ◽  
Shipeng Geng ◽  
Cong Lin ◽  
Lukas Palatinus ◽  
...  

Abstract CeNbO4+δ, a family of oxygen hyperstoichiometry materials with varying oxygen content (CeNbO4, CeNbO4.08, CeNbO4.25, CeNbO4.33) that shows mixed electronic and oxide ionic conduction, has been known for four decades. However, the oxide ionic transport mechanism has remained unclear due to the unknown atomic structures of CeNbO4.08 and CeNbO4.33. Here, we report the complex (3 + 1)D incommensurately modulated structure of CeNbO4.08, and the supercell structure of CeNbO4.33 from single nanocrystals by using a three-dimensional electron diffraction technique. Two oxide ion migration events are identified in CeNbO4.08 and CeNbO4.25 by molecular dynamics simulations, which was a synergic-cooperation knock-on mechanism involving continuous breaking and reformation of Nb2O9 units. However, the excess oxygen in CeNbO4.33 hardly migrates because of the high concentration and the ordered distribution of the excess oxide ions. The relationship between the structure and oxide ion migration for the whole series of CeNbO4+δ compounds elucidated here provides a direction for the performance optimization of these compounds.


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