Investigation of AFeO3 (A=Ba, Sr) Perovskites for the Oxidative Dehydrogenation of Light Alkanes under Chemical Looping Conditions

Abstract Oxidative dehydrogenation (ODH) of light alkanes to produce C 2 −C 3 olefins is a promising alternative to conventional steam cracking. Perovskite oxides are emerging as efficient catalysts for this process due to their unique properties such as high oxygen storage capacity (OSC), reversible redox behavior, and tunability. Here, we explore AFeO 3 (A=Ba, Sr) bulk perovskites for the ODH of ethane and propane under chemical looping conditions (CL‐ODH). The higher OSC and oxygen mobility of SrFeO 3 perovskite contributed to its higher activity but lower olefin selectivity than its Ba counterpart. However, SrFeO 3 perovskite is superior in terms of cyclic stability over multiple redox cycles. Transformations of the perovskite to reduced phases including brownmillerite A 2 Fe 2 O 5 were identified by X‐ray diffraction (XRD) as a cause of performance degradation, which was fully reversible upon air regeneration. A pre‐desorption step was utilized to selectively tune the amount of lattice oxygen as a function of temperature and dwell time to enhance olefin selectivity while suppressing CO 2 formation from the deep oxidation of propane. Overall, SrFeO 3 exhibits promising potential for the CL‐ODH of light alkanes, and optimization through surface and structural modifications may further engineer well‐regulated lattice oxygen for maximizing olefin yield.