Abstract:Sm1.8Ce0.2CuO4-xCe0.9Gd0.1O1.95 (SCC-xCGO, x = 0-12 vol.%) composite cathodes supported on Ce0.9Gd0.1O1.95 (CGO) electrolyte are studied for applications in IT-SOFCs. Results show that Sm1.8Ce0.2CuO4 material is chemically compatible with Ce0.9Gd0.1O1.95 at 1000 °C. The composite electrode exhibits optimum microstructure and forms good contact with the electrolyte after sintering at 1000 °C for 4 h. The polarization resistance (Rp) reduces to the minimum value of 0.17 Ω cm 2 at 750 °C in air for SCC-CGO06 comp… Show more
“…[ 342 ] In another case, a Sm 1.8 Ce 0.2 CuO 4 -Ce 0.9 Gd 0.1 O 1.95 composite cathode materials was prepared and an enhanced electrode performance was also observed as compared with the performance of a pure Sm 1.8 Ce 0.2 CuO 4 electrode. [ 343 ] It seemed that improving ionic conductivity of the Sm 1.8 Ce 0.2 CuO 4 electrode could promote its activity for ORR. However, the main drawback of Nd 2 CuO 4 and Sm 2 CuO 4 materials for application in SOFCs was their low electrical conductivities (less than 1 S cm −1 ) at working temperature.…”
Section: Ruddlesden-popper-type Metal Oxidesmentioning
Solid oxide fuel cells (SOFCs) represent one of the cleanest and most efficient options for the direct conversion of a wide variety of fuels to electricity. For example, SOFCs powered by natural gas are ideally suited for distributed power generation. However, the commercialization of SOFC technologies hinges on breakthroughs in materials development to dramatically reduce the cost while enhancing performance and durability. One of the critical obstacles to achieving high‐performance SOFC systems is the cathodes for oxygen reduction reaction (ORR), which perform poorly at low temperatures and degrade over time under operating conditions. Here a comprehensive review of the latest advances in the development of SOFC cathodes is presented: complex oxides without alkaline earth metal elements (because these elements could be vulnerable to phase segregation and contaminant poisoning). Various strategies are discussed for enhancing ORR activity while minimizing the effect of contaminant on electrode durability. Furthermore, some of the critical challenges are briefly highlighted and the prospects for future‐generation SOFC cathodes are discussed. A good understanding of the latest advances and remaining challenges in searching for highly active SOFC cathodes with robust tolerance to contaminants may provide useful guidance for the rational design of new materials and structures for commercially viable SOFC technologies.
“…[ 342 ] In another case, a Sm 1.8 Ce 0.2 CuO 4 -Ce 0.9 Gd 0.1 O 1.95 composite cathode materials was prepared and an enhanced electrode performance was also observed as compared with the performance of a pure Sm 1.8 Ce 0.2 CuO 4 electrode. [ 343 ] It seemed that improving ionic conductivity of the Sm 1.8 Ce 0.2 CuO 4 electrode could promote its activity for ORR. However, the main drawback of Nd 2 CuO 4 and Sm 2 CuO 4 materials for application in SOFCs was their low electrical conductivities (less than 1 S cm −1 ) at working temperature.…”
Section: Ruddlesden-popper-type Metal Oxidesmentioning
Solid oxide fuel cells (SOFCs) represent one of the cleanest and most efficient options for the direct conversion of a wide variety of fuels to electricity. For example, SOFCs powered by natural gas are ideally suited for distributed power generation. However, the commercialization of SOFC technologies hinges on breakthroughs in materials development to dramatically reduce the cost while enhancing performance and durability. One of the critical obstacles to achieving high‐performance SOFC systems is the cathodes for oxygen reduction reaction (ORR), which perform poorly at low temperatures and degrade over time under operating conditions. Here a comprehensive review of the latest advances in the development of SOFC cathodes is presented: complex oxides without alkaline earth metal elements (because these elements could be vulnerable to phase segregation and contaminant poisoning). Various strategies are discussed for enhancing ORR activity while minimizing the effect of contaminant on electrode durability. Furthermore, some of the critical challenges are briefly highlighted and the prospects for future‐generation SOFC cathodes are discussed. A good understanding of the latest advances and remaining challenges in searching for highly active SOFC cathodes with robust tolerance to contaminants may provide useful guidance for the rational design of new materials and structures for commercially viable SOFC technologies.
“…We studied the electrochemical performance of Sm 2−x Ce x CuO 4 and the ASR of Sm 1.8 Ce 0.2 CuO 4 was found to be 1.16 Ω cm 2 at 700 °C [17]. Further research on the oxygen reduction kinetics of these cuprate cathodes always found that the charge transfer reaction was the rate limiting step [16], [17], [18], [19] and [20]. Thus, enhancing the oxygen reduction activity of these cathode materials is crucial for the development of novel IT-SOFC cathode.…”
Different amount of metal silver particles are infiltrated into porous Sm 1.8 Ce 0.2 CuO 4 (SCC) scaffold to form SCC-Ag composite cathodes. The chemical stability, microstructure evolution and electrochemical performance of the composite cathode are investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), and AC impedance spectroscopy respectively. The composite cathode exhibits enhanced chemical stability. The metal Ag remains un-reacted with SCC and Ce 0.9 Gd 0.1 O 1.95 (CGO) at 800 °C for 72 h. The polarization resistance of the composite cathode decreases with the addition of metal Ag. The optimum cathode SCC-Ag05 exhibits the lowest area specific resistance (ASR, 0.43 Ω cm 2) at 700 °C in air. Investigation shows that metal Ag accelerates the charge transfer process in the composite cathode, and the rate limiting step for electrochemical oxygen reduction reaction (ORR) changes to oxygen dissociation and diffusion process.
“…Many cobalt-containing perovskite oxides (like Sm0.5Sr0.5CoO3-δ [6][7][8], La1-xSrxCoO3-δ [9][10][11][12][13][14], La1-xSrxCo1-yFeyO3-δ [15,16], Ba1-xSrxCo1-yFeyO3-δ [17][18][19]) have been developed as cathode materials for intermediate temperature range (500-700 ℃), which demonstrate that excellent ionic and electronic conductivities extend the triple-phase boundary (TPB) region from the cathodeelectrolyte interface into the bulk of the cathode. The powders of these cathode materials are made typically by sol-gel [20][21][22], solid state [23][24][25], combustion [26][27][28], acetic-acrylic [5,29,30], citric acid-EDTA [4,9,10,16,31], solid-liquid [32][33][34][35] etc.…”
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