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From the Precursor to the Active State: Monitoring Metamorphosis of Electrocatalysts During Water Oxidation by In Situ Spectroscopy

机译:从前体到活性状态:通过原位光谱法监测水氧化过程中电催化剂的变态

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摘要

In situ Raman and in situ EPR spectroscopy in combination with electrochemistry have been used to investigate the behavior of mixed cobalt nickel and cobalt copper oxides in the oxygen evolution reaction (OER). All experiments were carried out in homemade electrochemical cells using 0.1 M KOH as the electrolyte. The OER activities vary depending on the annealing conditions of the catalyst precursors, also reflected by different behaviours during the in situ spectroscopic experiments. The different activity of the Co/Ni oxides is most likely related to the formation of either gamma- or beta-NiO(OH), characterized by distinct features in the Raman spectra. Thus, a higher percentage of beta-NiO(OH) is present in the more active catalyst. A different behaviour of Co/Cu catalysts has been shown by in situ Raman spectroscopy too, but the active phase could not be identified because of missing spectral features. However, in situ EPR spectroscopy revealed the partial dissolution of Cu(II), suggesting the formation of a Co-enriched oxide/hydroxide surface.
机译:原位拉曼和原位EPR光谱与电化学结合使用,用于研究混合钴镍和钴铜氧化物在氧进化反应中的行为(OER)。所有实验均使用0.1M KOH作为电解质在自制电化学电池中进行。 OER活性根据催化剂前体的退火条件而变化,在原位光谱实验期间也反映了不同行为。 Co / Ni氧化物的不同活性最可能与γ-或β-NiO(OH)的形成有关,其特征在于拉曼光谱中的不同特征。因此,更高百分比的β-niO(OH)存在于更活性的催化剂中。已经通过原位拉曼光谱显示了CO / Cu催化剂的不同行为,但由于缺少光谱特征,不能识别活性相。然而,原位EPR光谱揭示了Cu(II)的部分溶解,表明形成共富氧化物/氢氧化物表面。

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