Studies of Ni-yttria-stabilized zirconia (YSZ) fuel electrode degradation mechanisms in solid oxide electrolysis cells (SOECs) are complicated by the different possible Ni-YSZ microstructures and compositions, and the variations in the H/HO ratio encountered in an electrolysis stack. Here we describe a life testing scheme aimed at providing survey results on degradation as a function of the HO-H composition, with life tests carried out at five different steam contents from 90% to 10%. A Ni-YSZ-supported symmetric cell geometry is employed both with and without infiltrated nanoscale gadolinia-doped ceria (GDC). Impedance spectroscopy is utilized to observe changes in electrochemical characteristics during the life test, and a transmission-line-based equivalent circuit is used to model the data. Post-test electrode microstructures were observed. The results suggest that the GDC infiltrant reduces the electrode polarization resistance and provides more stable electrode polarization over a range of conditions.
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http://dx.doi.org/10.1021/acs.nanolett.1c02937 | DOI Listing |
Membranes (Basel)
January 2025
Fort Hare Institute of Technology, University of Fort Hare, Private Bag X1314, Alice 5700, Eastern Cape, South Africa.
Recently, the recovery of metals extracted from the spent membrane electrode assemblies (MEAs) of fuel cells has attracted significant scientific attention due to its detrimental environmental impacts. Two major approaches, i.e.
View Article and Find Full Text PDFMembranes (Basel)
December 2024
Department of Chemical & Biological Engineering, Hanbat National University, Daejeon 34158, Republic of Korea.
This study addresses the critical challenge of carbon corrosion in proton exchange membrane fuel cells (PEMFCs) by developing hybrid supports that combine the high surface area of carbon black (CB) with the superior crystallinity and graphitic structure of carbon nanofibers (CNFs). Two commercially available CB samples were physically activated and composited with two types of CNFs synthesized via chemical vapor deposition using different carbon sources. The structure, morphology, and crystallinity of the resulting CNF-CB hybrid supports were characterized, and the performances of these hybrid supports in mitigating carbon corrosion and enhancing the PEMFC performance was evaluated through full-cell testing in collaboration with a membrane electrode assembly (MEA) manufacturer (VinaTech, Seoul, Republic, of Korea), adhering to industry-standard fabrication and evaluation procedures.
View Article and Find Full Text PDFSmall
January 2025
Center of Nanomaterials for Renewable Energy (CNRE), State Key Laboratory of Electrical Insulation and Power Equipment, School of Electrical Engineering, Xi'an Jiaotong University, Xi'an, Shaanxi, 710049, P. R. China.
The traditional perfluorosulfonic acid proton exchange membrane is crucial for proton exchange membrane fuel cells, but its high cost has impeded broader commercialization. In this study, a novel concept of a cost-effective and stable vertically aligned polydopamine-intercalated montmorillonite membrane (VAPMM) is introduced. 2D nanochannels formed within the lamellar structure of polydopamine-coated montmorillonite nanosheets provide a significant stable in-plane proton conductivity of 0.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
State Key Laboratory of Chemical Resource Engineering, College of Chemistry, Beijing University of Chemical Technology, Beijing 100029 China. Electronic address:
The design and screening of low cost and high efficiency oxygen reduction reaction (ORR) electrocatalysts is vital in the realms of fuel cells and metal-air batteries. Existing studies largely rely on the calculation of absorption free energy, a method established 20 years ago by Jens K. Nørskov.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Central South University, chemistry, CHINA.
The two-dimensional lamellar materials disperse platinum sites and minimize noble-metal usage for fuel cells, while mass transport resistance at the stacked layers spurs device failure with a significant performance decline in membrane electrode assembly (MEA). Herein, we implant porous and rigid sulfonated covalent organic frameworks (COF) into the graphene-based catalytic layer for the construction of steric mass-charge channels, which highly facilitates the activity of oxygen reduction reactions in both the rotating disk electrode (RDE) measurements and MEA device tests. Specifically, the normalized mass activity is remarkably boosted by 3.
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