Protonic ceramic electrochemical cells for hydrogen production and electricity generation: exceptional reversibility, stability, and demonstrated faradaic efficiency

We demonstrate exceptional performance for steam electrolysis at intermediate temperatures (500-650 °C) using protonic ceramic electrolyte cells comprised of the proton-permeable, high-activity mixed conductor PrBa 0.5 Sr 0.5 Co 1.5 Fe 0.5 O 5+ δ (PBSCF) as the air electrode, the highly proton-conductive and chemically stable perovskite oxide BaZr 0.4 Ce 0.4 Y 0.1 Yb 0.1 O 3 (BZCYYb4411) as the electrolyte, and a composite of Ni-BZCYYb4411 as the fuel electrode. Cells constructed from this material set have been shown previously to function efficiently in fuel cell mode. We demonstrate here reversible operation, enabling hydrogen production when excess electricity is available and immediate electricity generation from stored hydrogen when power demand is high. The cells are stable under cyclic operation and also under prolonged continuous operation in electrolysis mode, undergoing minimal loss in electrochemical characteristics after 500 h at 550 °C. Microstructurally optimized cells yield a remarkable current density of −1.80 A cm −2 at 600 °C and an operating voltage of 1.3 V, of which, based on an electrochemically deduced faradaic efficiency of 76%, −1.37 A cm −2 contributes to useful hydrogen. We demonstrate excellent performance and durability at intermediate temperatures (500-650 °C) upon reversible operation of an electrochemical cell incorporating a proton-permeable, high-activity mixed conducting oxide as the air electrode, a highly proton-conductive and chemically stable perovskite oxide as the electrolyte, and a composite of Ni and the electrolyte as the fuel electrode.