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Chemical Recognition of Active Oxygen Species on the Surface of Oxygen Evolution Reaction Electrocatalysts

机译:析氧反应电催化剂表面活性氧的化学识别

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摘要

Owing to the transient nature of the intermediates formed during the oxygen evolution reaction (OER) on the surface of transition metal oxides, their nature remains largely elusive by the means of simple techniques. The use of chemical probes is proposed, which, owing to their specific affinities towards different oxygen species, unravel the role played by these species on the OER mechanism. For that, tetraalkylammonium (TAA) cations, previously known for their surfactant properties, are introduced, which interact with the active oxygen sites and modify the hydrogen bond network on the surface of OER catalysts. Combining chemical probes with isotopic and pH‐dependent measurements, it is further demonstrated that the introduction of iron into amorphous Ni oxyhydroxide films used as model catalysts deeply modifies the proton exchange properties, and therefore the OER mechanism and activity.
机译:由于在过渡金属氧化物表面上的氧逸出反应(OER)期间形成的中间体的瞬态性质,通过简单的技术手段,它们的性质仍然难以捉摸。提出了使用化学探针的方法,由于其对不同氧种类的特定亲和力,因此可以阐明这些物质在OER机制中的作用。为此,引入了先前因其表面活性剂特性而闻名的四烷基铵(TAA)阳离子,该阳离子与活性氧位相互作用并修饰OER催化剂表面的氢键网络。将化学探针与同位素和pH依赖的测量相结合,进一步证明了将铁引入用作模型催化剂的非晶态羟基氧化镍薄膜中会极大地改变质子交换性能,从而改变OER机理和活性。

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