scholarly journals Compositional Engineering of a La1-xBaxCoO3-δ-(1-a) BaZr0.9Y0.1O2.95 (a = 0.6, 0.7, 0.8 and x = 0.5, 0.6, 0.7) Nanocomposite Cathodes for Protonic Ceramic Fuel Cells

Materials ◽  
2019 ◽  
Vol 12 (20) ◽  
pp. 3441
Author(s):  
Laura Rioja-Monllor ◽  
Carlos Bernuy-Lopez ◽  
Marie-Laure Fontaine ◽  
Tor Grande ◽  
Mari-Ann Einarsrud

Compositionally engineered a La1-xBaxCoO3-δ-(1-a) BaZr0.9Y0.1O2.95 (a = 0.6, 0.7, 0.8 and x = 0.5, 0.6, 0.7) (LBZ) nanocomposite cathodes were prepared by oxidation driven in situ exsolution of a single-phase material deposited on a BaZr0.9Y0.1O2.95 electrolyte. The processing procedure of the cathode was optimized by reducing the number of thermal treatments as the single-phase precursor was deposited directly on the electrolyte. The exsolution and firing of the cathodes occurred in one step. The electrochemical performance of symmetrical cells with the compositionally engineered cathodes was investigated by impedance spectroscopy in controlled atmospheres. The optimized materials processing gave web-like nanostructured cathodes with superior electrochemical performance for all compositions. The area specific resistances obtained were all below 12 Ω·cm2 at 400 °C and below 0.59 Ω·cm2 at 600 °C in 3% moist synthetic air. The resistances of the nominal 0.6 La0.5Ba0.5CoO3-δ-0.4 BaZr0.9Y0.1O2.95 and 0.8 La0.5Ba0.5CoO3-δ-0.2 BaZr0.9Y0.1O2.95 composite cathodes were among the lowest reported for protonic ceramic fuel cells cathodes in symmetrical cell configuration with ASR equal to 4.04 and 4.84 Ω·cm2 at 400 °C, and 0.21 and 0.27 Ω·cm2 at 600 °C, respectively.

Inorganics ◽  
2018 ◽  
Vol 6 (3) ◽  
pp. 83 ◽  
Author(s):  
Laura Rioja-Monllor ◽  
Sandrine Ricote ◽  
Carlos Bernuy-Lopez ◽  
Tor Grande ◽  
Ryan O’Hayre ◽  
...  

A novel exsolution process was used to fabricate complex all-oxide nanocomposite cathodes for Protonic Ceramic Fuel Cells (PCFCs). The nanocomposite cathodes with La0.5Ba0.5Co1/3Mn1/3Fe1/3O3−δ-BaZr1−zYzO3−δ nominal composition were prepared from a single-phase precursor via an oxidation-driven exsolution mechanism. The exsolution process results in a highly nanostructured and intimately interconnected percolating network of the two final phases, one proton conducting (BaZr1−zYzO3−δ) and one mixed oxygen ion and electron conducting (La0.5Ba0.5Co1/3Mn1/3Fe1/3O3−δ), yielding excellent cathode performance. The cathode powder is synthesized as a single-phase cubic precursor by a modified Pechini route followed by annealing at 700 °C in N2. The precursor phase is exsolved into two cubic perovskite phases by further heat treatment in air. The phase composition and chemical composition of the two phases were confirmed by Rietveld refinement. The electrical conductivity of the composites was measured and the electrochemical performance was determined by impedance spectroscopy of symmetrical cells using BaZr0.9Y0.1O2.95 as electrolyte. Our results establish the potential of this exsolution method where a large number of different cations can be used to design composite cathodes. The La0.5Ba0.5Co1/3Mn1/3Fe1/3O3−δ-BaZr0.9Y0.1O2.95 composite cathode shows the best performance of 0.44 Ω∙cm2 at 600 °C in 3% moist synthetic air.


2019 ◽  
Vol 91 (1) ◽  
pp. 1075-1083
Author(s):  
Hiroyuki Shimada ◽  
Toshiaki Yamaguchi ◽  
Yuki Yamaguchi ◽  
Yoshinobu Fujishiro ◽  
Yasunobu Mizutani

2020 ◽  
Vol 40 (8) ◽  
pp. 3104-3110
Author(s):  
Chaoliang Geng ◽  
Xinxi Yu ◽  
Piaopiao Wang ◽  
Jigui Cheng ◽  
Tao Hong

2018 ◽  
Vol 44 (7) ◽  
pp. 8423-8426 ◽  
Author(s):  
EunKyong Shin ◽  
Minho Shin ◽  
Hanjin Lee ◽  
Jong-Sung Park

2020 ◽  
Vol 10 (7) ◽  
pp. 2481 ◽  
Author(s):  
Artem Tarutin ◽  
Nikolay Danilov ◽  
Julia Lyagaeva ◽  
Dmitry Medvedev

The present paper reports the preparation of multilayer protonic ceramic fuel cells (PCFCs) using a single sintering step. The success of this fabrication approach is due to two main factors: the rational choice of chemically and mechanically compatible components, as well as the selection of a convenient preparation (tape calendering) method. The PCFCs prepared in this manner consisted of a 30 µm BaCe0.5Zr0.3Dy0.2O3–δ (BCZD) electrolyte layer, a 500 μm Ni–BCZD supporting electrode layer and a 20 μm functional Pr1.9Ba0.1NiO4+δ (PBN)–BCZD cathode layer. These layers were jointly co-fired at 1350 °C for 5 h to reach excellent gas-tightness of the electrolyte and porous structures for the supported and functional electrodes. The adequate fuel cell performance of this PCFC design (400 mW cm−2 at 600 °C) demonstrates that the tape calendering method compares well with such conventional laboratory PCFC preparation techniques such as co-pressing and tape-casting.


2015 ◽  
Vol 2 (8) ◽  
pp. 1106-1110 ◽  
Author(s):  
Cecilia Solís ◽  
Laura Navarrete ◽  
Francesco Bozza ◽  
Nikolaos Bonanos ◽  
José M. Serra

2018 ◽  
Vol 6 (29) ◽  
pp. 14188-14194 ◽  
Author(s):  
Toshiaki Matsui ◽  
Kohei Manriki ◽  
Kazunari Miyazaki ◽  
Hiroki Muroyama ◽  
Koichi Eguchi

A new oxygen reduction electrocatalyst of barium lanthanide cobaltate of Ba4Sr2Sm2Co4O15 (BSSC) for composite cathodes of proton-conducting ceramic fuel cells.


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