Self-Assembly Dual Active Site Nanocomposite Anode Ce 0.6 Mn 0.3 Fe 0.1 O 2-δ /NiFe/MnO x for Electrooxidative Dehydrogenation of Ethane to Ethylene.

As the demand for ethylene grows continuously in industry, conversion of ethane to ethylene has become more and more important; however, it still faces fundamental challenges of low ethane conversion, low ethylene selectivity, overoxidation, and instability of catalysts. Electrooxidative dehydrogenation of ethane (EODHE) in a solid oxide electrolysis cell (SOEC) is an alternative process. Here, a multiphase oxide Ce 0.6 Mn 0.3 Fe 0.1 O 2-δ -NiFe-MnO x has been fabricated by a self-assembly process and utilized as the SOEC anode material for EODHE. The highest ethane conversions reached 52.23% with 94.11% ethylene selectivity at the anode side and CO with 10.9 mL min -1 cm -2 at the cathode side, at 1.8 V at 700 °C. The remarkable electrooxidative performance of CMF-NiFe-MnO x is ascribed to the NiFe alloy and MnO x nanoparticles and improvement of the concentration of oxygen vacancies within the fluorite substrate, generating dual active sites for C 2 H 6 adsorption, dehydrogenation, and selective transformation of hydrogen without overoxidizing the ethylene generated. Such a tailored strategy achieves no significant degradation observed after 120 h of operation and constitutes a promising basis for EODHE.