• Marina, Olga A.
• Coyle, Christopher A.
• Pederson, Larry R.
• Edwards, Danny J.
• Thomsen, Edwin C.
• Coffey, Greg W.

Abstract

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 800oC in synthetic coal gas containing 0.5 to 10 ppm phosphorus, 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 Ni3P, Ni5P2, Ni12P5 and Ni2P 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. Thermodynamic calculations predict that formation of the first binary nickel phosphide phase is possible at sub-parts per billion concentrations in coal gas at temperatures relevant to fuel cell operation. 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 very low dependence on phosphorus concentration, attributed to phosphorus activity control within the anode by bulk nickel phosphide products.

Topics

• impedance spectroscopy
• surface
• grain
• nickel
• phase
• forming
• Phosphorus