Massué Cyriac, Huang Xing, Tarasov Andrey, Ranjan Chinmoy, Cap Sébastien, Schlögl Robert
Department of Inorganic Chemistry, Fritz-Haber-Institute of the Max-Planck Society, 14195, Berlin, Germany.
Department of Heterogenous Reactions, Max-Planck Institute for Chemical Energy Conversion, 45470, Mülheim-an-der-Ruhr, Germany.
ChemSusChem. 2017 May 9;10(9):1958-1968. doi: 10.1002/cssc.201601864. Epub 2017 Apr 12.
Water splitting for hydrogen production in acidic media has been limited by the poor stability of the anodic electrocatalyst devoted to the oxygen evolution reaction (OER). To help circumvent this problem we have synthesized a class of novel Ir oxohydroxides by rapid microwave-asisted hydrothermal synthesis, which bridges the gap between electrodeposited amorphous IrO films and crystalline IrO electrocatalysts prepared by calcination routes. For electrode loadings two orders of magnitude below current standards, the synthesized compounds present an unrivalled combination of high activity and stability under commercially relevant OER conditions in comparison to reported benchmarks, without need for pretreatment. The best compound achieved a lifetime 33 times longer than the best commercial Ir benchmark. Thus, the reported efficient synthesis of an Ir oxohydroxide phase with superior intrinsic OER performance constitutes a major step towards the targeted design of cost-efficient Ir based OER electrocatalysts for acidic media.
在酸性介质中用于制氢的水分解反应,一直受到用于析氧反应(OER)的阳极电催化剂稳定性较差的限制。为了帮助解决这个问题,我们通过快速微波辅助水热合成法合成了一类新型的铱羟基氧化物,它填补了电沉积非晶态IrO薄膜与通过煅烧路线制备的晶态IrO电催化剂之间的空白。对于比当前标准低两个数量级的电极负载量,与已报道的基准相比,所合成的化合物在商业相关的OER条件下展现出高活性和稳定性的无与伦比的组合,且无需预处理。最佳化合物的寿命比最佳商业铱基准长33倍。因此,所报道的具有优异本征OER性能的铱羟基氧化物相的高效合成,是朝着设计用于酸性介质的具有成本效益的铱基OER电催化剂这一目标迈出的重要一步。