Ieva A. Cechanaviciute, Rajini P. Antony, Lars Banko, Thomas Quast, Saika Pokharel, Alfred Ludwig, Olga A. Krysiak, Wolfgang Schuhmann
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引用次数: 0
摘要
高性能水电解电催化剂的发现具有十分重要的意义。我们使用基于薄膜材料库中广泛材料组成的高通量筛选的催化剂发现策略来识别在碱性电解质中对析氢反应具有高活性的贵金属-贫多金属组合物。我们使用一个包含Mo, Ag, Ti和Ru的季元材料库,通过组合磁控溅射在直径为10 cm的晶圆上制造,提供342个测量区域。令人惊讶的是,相对较低Ru含量的二元Mo - Ru催化剂组合物表现出最高的活性。采用基于聚合物/金属前驱体的喷雾技术,用Mo - Ru撞击组合物修饰了Ni泡沫电极,并在膜电极组件(MEA)配置的模型电解槽中进行了评估。在−2 a cm−2的较高电流密度下,电极的过电位极低,仅为132 mV;在−1 a cm−2的电流密度下,电极的电解稳定性为24 h,初始电极调节后没有明显的退化。
Discovery of Highly Active Noble-Metal-Lean Mo−Ru Electrocatalysts for Hydrogen Evolution
The discovery of high-performance electrocatalysts for water electrolysis is highly important. We use a strategy for catalyst discovery based on high-throughput screening of a broad range of materials compositions on a thin-film materials library to identify noble-metal-lean multi-metal compositions with high activity towards the hydrogen evolution reaction in alkaline electrolyte. We demonstrate this strategy using a quaternary materials library containing Mo, Ag, Ti, and Ru fabricated by combinatorial magnetron sputtering on a 10 cm diameter wafer providing 342 measurement areas. Surprisingly, binary Mo−Ru-containing catalyst compositions with comparatively low Ru content exhibited the highest activity. Using the polymer/metal precursor-based spray technique, Ni foam electrodes were modified with the Mo−Ru hit compositions and evaluated in a model electrolyzer in membrane electrode assembly (MEA) configuration. The electrodes showed a very low overpotential of only 132 mV at a comparatively high current density of −2 A cm−2 and a 24 h electrolysis stability at −1 A cm−2 with no observable degradation after the initial electrode conditioning.
期刊介绍:
ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.