Cubic perovskite SrCoO 3−δ was successfully prepared through simple anion F-doping and demonstrated great OER performance.
Driven by the increasing global energy demand, the development of innovative energy conversion and storage systems is becoming more and more urgent. As one of the attractive means, water splitting has attracted widespread attention because of its great potential in storing electricity in the form of chemical fuel which also makes it a promising solution to the utilization of non-grid electricity generated by solar or wind. The oxygen evolution reaction (OER) is generally deemed as the key rate-limiting step of water splitting, and thus studying efficient OER electrocatalysts with a low overpotential and good stability is of vital importance. Here, we successfully prepared an OER catalyst with excellent electrochemical performance through a simple anion doping. Firstly, a stable cubic perovskite SrCoO 3−δ was prepared by anion F-doping instead of traditional A and/or B site doping. Secondly, SrCoO 2.85−δF 0.15 demonstrates excellent OER activity superior to its parent hexagonal compound H-Sr 2Co 2O 5 and those perovskites prepared via complicated A- and/or B-site doping. DFT calculations and XPS investigations reveal that the cubic structure and the highly oxidative oxygen species (O 2 2−/O −) via F − doping jointly contribute to the better OER properties of SrCoO 2.85−δF 0.15. Our work brings forth a promising strategy to stabilize cubic structures from hexagonal ones via a simple anion doping strategy, which may open a new avenue for the development of even more effective OER catalysts and may be applied in many other fields related to structure transformation, in addition to energy and catalysis fields.