Solid-oxide fuel cell operated on in situ catalytic decomposition products of liquid hydrazine

Abstract

Hydrazine was examined as a fuel for a solid-oxide fuel cell (SOFC) that employed a typical nickel-based anode. An in situ catalytic decomposition of hydrazine at liquid state under room temperature and ambient pressure before introducing to the fuel cell was developed by applying a Ba 0.5Sr 0.5Co 0.8Fe 0.2O 3− δ (BSCF) oxide catalyst. Catalytic testing demonstrated that liquid N 2H 4 can be decomposed to gaseous NH 3 and H 2 at a favorable rate and at a temperature as low as 20 °C and H 2 selectivity reaching values as high as 10% at 60 °C. Comparable fuel cell performance was observed using either the in situ decomposition products of hydrazine or pure hydrogen as fuel. A peak power density of ∼850 mW cm −2 at 900 °C was obtained with a typical fuel cell composed of scandia-stabilized zirconia and La 0.8Sr 0.2MnO 3 cathode. The high energy and power density, easy storage and simplicity in fuel delivery make it highly attractive for portable applications.