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Efficient oxygen evolution electrocatalysis in acid by a perovskite with face-sharing IrO6 octahedral dimers

机译:钙钛矿与面部共享的IrO6八面体二聚体在酸中的高效氧释放电催化

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摘要

The widespread use of proton exchange membrane water electrolysis requires the development of more efficient electrocatalysts containing reduced amounts of expensive iridium for the oxygen evolution reaction (OER). Here we present the identification of 6H-phase SrIrO3 perovskite (6H-SrIrO3) as a highly active electrocatalyst with good structural and catalytic stability for OER in acid. 6H-SrIrO3 contains 27.1 wt% less iridium than IrO2, but its iridium mass activity is about 7 times higher than IrO2, a benchmark electrocatalyst for the acidic OER. 6H-SrIrO3 is the most active catalytic material for OER among the iridium-based oxides reported recently, based on its highest iridium mass activity. Theoretical calculations indicate that the existence of face-sharing octahedral dimers is mainly responsible for the superior activity of 6H-SrIrO3 thanks to the weakened surface Ir-O binding that facilitates the potential-determining step involved in the OER (i.e., O* + H2O → HOO* + H+ + e¯).
机译:质子交换膜水电解的广泛应用要求开发更有效的电催化剂,其中包含用于氧气析出反应(OER)的数量减少的昂贵铱。在这里,我们提出鉴定6H相SrIrO3钙钛矿(6H-SrIrO3)作为高活性电催化剂,对酸中的OER具有良好的结构和催化稳定性。 6H-SrIrO3的铱比IrO2少27.1%(重量),但其铱的质量活性比酸性OER的基准电催化剂IrO2高约7倍。 6H-SrIrO3是最近报道的铱基氧化物中OER活性最高的催化材料,基于其最高的铱质量活性。理论计算表明,由于表面Ir-O结合力减弱,OER参与的电势确定步骤(即O * + H2O)的存在,面部共享的八面体二聚体的存在主要是6H-SrIrO3较高活性的原因。 →HOO * + H + +e¯)。

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