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Edge reactivity and water-assisted dissociation on cobalt oxide nanoislands

机译:氧化钴纳米岛上的边缘反应性和水辅助解离

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摘要

Transition metal oxides show great promise as Earth-abundant catalysts for the oxygen evolution reaction in electrochemical water splitting. However, progress in the development of highly active oxide nanostructures is hampered by a lack of knowledge of the location and nature of the active sites. Here we show, through atom-resolved scanning tunnelling microscopy, X-ray spectroscopy and computational modelling, how hydroxyls form from water dissociation at under coordinated cobalt edge sites of cobalt oxide nanoislands. Surprisingly, we find that an additional water molecule acts to promote all the elementary steps of the dissociation process and subsequent hydrogen migration, revealing the important assisting role of a water molecule in its own dissociation process on a metal oxide. Inspired by the experimental findings, we theoretically model the oxygen evolution reaction activity of cobalt oxide nanoislands and show that the nanoparticle metal edges also display favourable adsorption energetics for water oxidation under electrochemical conditions.
机译:过渡金属氧化物作为富氧催化剂在电化学水分解中的氧气释放反应中具有广阔的前景。然而,由于缺乏对活性位点的位置和性质的了解,阻碍了高活性氧化物纳米结构的发展。在这里,我们展示了通过原子分辨扫描隧道显微镜,X射线光谱学和计算建模,如何在钴氧化物纳米岛的钴边缘边缘配位下水解离形成羟基。令人惊讶地,我们发现另外的水分子起到促进离解过程和随后氢迁移的所有基本步骤的作用,揭示了水分子在其自身对金属氧化物的离解过程中的重要辅助作用。受实验结果的启发,我们从理论上模拟了氧化钴纳米岛的析氧反应活性,并表明纳米粒子的金属边缘在电化学条件下对水氧化也显示出良好的吸附能。

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