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在碱性介质中,钙钛矿基表面上的氧气电催化降解动力学。

Degradation Kinetics during Oxygen Electrocatalysis on Perovskite-Based Surfaces in Alkaline Media.

机构信息

Institute for Materials in Electrical Engineering and Information Technology (IWE2), RWTH Aachen University of Technology , D-52074 Aachen, Germany.

出版信息

Langmuir. 2018 Jan 30;34(4):1347-1352. doi: 10.1021/acs.langmuir.7b03733. Epub 2018 Jan 18.

Abstract

The oxygen evolution reaction (OER) during alkaline water electrolysis is the bottleneck of water splitting. Perovskite materials have been particularly proposed as good and economically reasonable electrocatalysts for the OER, showing promise and advantages with respect to classic metallic electrodes. However, the degradation of perovskites during catalysis limits their service lifetime. Recently, the material BaCoTiO:CoO was shown to be electrocatalytically and chemically stable during water electrolysis even under industrially relevant conditions. The lifetime of this perovskite-based system is prolonged by a factor of 10 in comparison to that of PrBaCoO and is comparable to that of industrially applied electrodes. Here we report on the degradation kinetics of several OER catalysts at room temperature, comparatively studied by monitoring the oxygen evolution at microelectrodes. A decrease in the reaction rate within a maximum of 60 s is observed, which is related to chemical and/or structural changes at the oxide surface.

摘要

在碱性水电解过程中,氧气的析出反应(OER)是其瓶颈。钙钛矿材料作为 OER 的电催化剂具有很好的经济性,相对于经典的金属电极具有优势和潜力。然而,在催化过程中钙钛矿的降解限制了其使用寿命。最近,研究表明,在工业相关条件下,即使在水分解过程中,BaCoTiO:CoO 材料在电化学和化学上都是稳定的。与 PrBaCoO 相比,这种基于钙钛矿的系统的使用寿命延长了 10 倍,与工业应用的电极相当。在这里,我们报告了在室温下对几种 OER 催化剂进行的降解动力学研究,通过监测微电极上的氧气析出来进行比较。在最多 60 秒内观察到反应速率的下降,这与氧化物表面的化学和/或结构变化有关。

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