Noble‐Metal‐Assisted Fast Interfacial Oxygen Migration with Topotactic Phase Transition in Perovskite Oxides

Transition-metal perovskite oxides constitute a series of functional material systems for electronics, catalysis and energy-conversion processes, in which oxygen migration and evolution play a key role. However, the stable metal-oxygen (M-O) bond forms large energy barrier inhibiting ion diffusion. Therefore, seeking efficient and facile approaches to accelerate oxygen kinetics has become a significant issue. Here, the interaction (interfacial charge transfer and cooperative bonding) between noble metal (Pt, Ag) and perovskites oxide (SrCoO3-delta) is employed to weaken (M-O) bond and decrease the energy barrier of oxygen migration. Noble metal layers serving as oxygen pumps can continuously extract oxygen from oxide films to atmosphere. The temperature of topotactic phase transition from perovskite (SrCoO3) to brownmillerite (SrCoO2.5) is remarkably lowered from 200 K to room temperature. Furthermore, this approach can also be applied to SrFeO3 for similar topotactic phase reduction by moderate thermal activation. Our finding paves a promising and general pathway to achieve fast oxygen migration in perovskite oxides, with important application prospect in low-temperature electrodes and high-activity catalysis interface.