Degradation mechanisms of SOFC anodes in coal gas containing phosphorus

• Published in: Solid state ionics 2010-03, Vol.181 (8), p.430-440
• Main Authors: Marina, O.A., Coyle, C.A., Thomsen, E.C., Edwards, D.J., Coffey, G.W., Pederson, L.R.
• Format: Article
• Language: English
• Subjects: 01 COAL, LIGNITE, AND PEAT; 30 DIRECT ENERGY CONVERSION; ADSORPTION; ANODES; COAL GAS; Contaminant; Degradation; DIFFUSION; Electrolytic cells; Environmental Molecular Sciences Laboratory; FRACTURES; FUEL CELLS; IMPEDANCE; Ni/YSZ anode; NICKEL; Nickel phosphide; NICKEL PHOSPHIDES; Nickel phosphorus interaction; Phosphides; PHOSPHORUS; SOFC; SOLID OXIDE FUEL CELLS; SPECTROSCOPY; Surface chemistry; THERMODYNAMICS
• ISSN: 0167-2738; 1872-7689
• DOI: 10.1016/j.ssi.2010.01.018

The interaction of phosphorus in synthetic coal gas with the nickel-based anode of solid oxide fuel cells has been investigated. Tests with both anode-supported and electrolyte-supported button cells were performed at 700 to 800 °C in synthetic coal gas containing 0.5 to 10 ppm phosphorus, which was introduced as phosphine. Two primary modes of degradation were observed. The most obvious was the formation of a series of bulk nickel phosphide phases, of which Ni 3P, Ni 5P 2, Ni 12P 5 and Ni 2P were identified. Phosphorus was essentially completely captured by the anode, forming a sharp boundary between converted and unconverted anode portions. These products partially coalesced into large grains, which eventually affected electronic percolation through the anode support. From thermodynamic calculations, formation of the first binary nickel phosphide phase is possible at phosphorus concentrations < 1 ppb in coal gas at typical fuel cell operating temperatures. A second mode of degradation is attributed to surface diffusion of phosphorus to the active anode/electrolyte interface to form an adsorption layer. Direct evidence for the presence of such an adsorption layer on nickel was obtained by surface spectroscopies on fracture surfaces. Further, cell performance losses were observed well before the entire anode was converted to bulk nickel phosphide. Impedance spectroscopy revealed that these losses were primarily due to growth in electrodic resistance, whereas large ohmic increases were visible when the entire anode was converted to nickel phosphide phases. The rate of resistance growth for anode-supported cells showed a low dependence on phosphorus concentration, attributed to phosphorus activity control within the anode by bulk nickel phosphide products.