Instability of Sulfate and Selenate Solid Acids in Fuel Cell Environments

Abstract

The chemical and thermal stability of several solid acid compounds under fuel cell operating conditions has been investigated, primarily by thermogravimetric methods. Thermal decomposition of CsHSO_4, a material which has shown promise as an alternative electrolyte for proton exchange membrane (PEM) fuel cells, initiates at ∼175°C under inert conditions. The overall decomposition process can be expressed as 2CsHSO_4 → Cs_2SO_4 + H_2O + SO_3 with Cs_2S_2O_7 appearing as an intermediate byproduct at slow heating rates. Under reducing conditions, chemical decomposition can occur via reaction with hydrogen according to 2CsHSO_4 + 4H_2 → Cs_2SO_4 + 4H_2O + H_2S. In the absence of fuel cell catalysts, this reduction reaction is slow; however, materials such as Pt, Pd, and WC are highly effective in catalyzing the reduction of sulfur and the generation of H_2S. In the case of M_3H(XO_4)_2 compounds, where M = Cs, NH_4, or Rb and X = S or Se, a similar reduction reaction occurs:  2M_3H(XO_4)_2 + 4H_2 → 3M_2XO_4 + 4H_2O + H_2X. In an operational fuel cell based on CsHSO_4, performance degraded with time, presumably as a result of H_2S poisoning of the anode catalyst. The performance loss was recoverable by exposure of the fuel cell to air at 160 °C.

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