Efficient Energy Storage via Methane Production Using Protonic Ceramic Electrochemical Cells

Abstract

Protonic ceramic electrochemical cells (PCECs) are promising energy storage technologies due to their high performance and ability to convert CO2 into value-added chemicals. However, there are many fundamental aspects of this technology that require investigation to better understand its interactions and opportunities. Thus, this paper focuses on the development of a steady-state PCEC model, encompassing intricate details of reactive porous-media transport, elementary catalytic chemistry, and electrochemistry within unit cells. The model is calibrated and validated using experimental data. The model presents the rate of methane production at different temperatures and revealed that efficient PCEC for co-electrolysis of CO2 and H2O is operated in the temperature range of 420–470 °C and the optimum being 450 °C at the rate of 0.0391 moldm−3 min−1. It provides insights into the effects of overpotentials on cell performance. At a current density of 3000 A/m2 the ohmic, concentration, and activation overpotentials amount to 0.65, 0.004, and 0.19 V, respectively. The results obtained from the model highlight the potential of PCECs as efficient CO2 sinks for decarbonization purposes and as a means of methane production. Furthermore, the model's findings offer valuable guidance for the design, selection of stacks, and choice of building materials in PCEC systems. The potential applications of PCECs as real-life fuel utilization technologies are justified with improved material development to reduce cell overpotentials, opening doors for scale-up and eventual commercialization. These findings contribute to the development of sustainable energy systems and advance the pursuit of decarbonization goals.