摘要
Graphical Order up : B-site cation-ordered double perovskites Ba 2 Bi x Sc 0.2 Co 1.8− x exhibited ultrahigh catalytic activity and favorable stability for the oxygen evolution reaction (OER) in alkaline solution. The critical role of the ordered [Co 2+ ] and [Sc 3+ , Bi 5+ , Co 3+ ] dual environments account for the high OER activity, representing a new class of promising electrocatalysts applied in energy storage and conversion systems. Simple disordered perovskite oxides have been intensively exploited as promising electrocatalysts for the oxygen evolution reaction (OER) towards their application in water splitting, reversible fuel cells, and rechargeable metal-air batteries. Here, the B-site cation-ordered double perovskites Ba 2 Bi x Sc 0.2 Co 1.8− x O 6−δ , with two types of cobalt local environments, are demonstrated to be superior electrocatalysts for OER in alkaline solution, demonstrating ultrahigh catalytic activity. In addition, no obvious performance degradation is observed for the Ba 2 Bi 0.1 Sc 0.2 Co 1.7 O 6−δ sample after a continuous chronopotentiometry test. The critical role of the ordered [Co 2+ ] and [Sc 3+ , Bi 5+ , Co 3+ ] dual environments in improving OER activity is exhibited. These results indicate that B-site cation-ordered double perovskite oxides may represent a new class of promising electrocatalysts for the OER in sustainable energy storage and conversion systems.
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