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Bifunctional non-noble metal oxide nanoparticle electrocatalysts through lithium-induced conversion for overall water splitting

机译:锂诱导转化双功能非贵金属氧化物纳米粒子电催化剂的总水分解

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摘要

Developing earth-abundant, active and stable electrocatalysts which operate in the same electrolyte for water splitting, including oxygen evolution reaction and hydrogen evolution reaction, is important for many renewable energy conversion processes. Here we demonstrate the improvement of catalytic activity when transition metal oxide (iron, cobalt, nickel oxides and their mixed oxides) nanoparticles (~20 nm) are electrochemically transformed into ultra-small diameter (2–5 nm) nanoparticles through lithium-induced conversion reactions. Different from most traditional chemical syntheses, this method maintains excellent electrical interconnection among nanoparticles and results in large surface areas and many catalytically active sites. We demonstrate that lithium-induced ultra-small NiFeOx nanoparticles are active bifunctional catalysts exhibiting high activity and stability for overall water splitting in base. We achieve 10 mA cm−2 water-splitting current at only 1.51 V for over 200 h without degradation in a two-electrode configuration and 1 M KOH, better than the combination of iridium and platinum as benchmark catalysts.
机译:在许多可再生能源转化过程中,开发出在同一电解质中用于分解水的富含地球,活性和稳定的电催化剂非常重要。在这里,我们证明了当过渡金属氧化物(铁,钴,氧化镍和它们的混合氧化物)纳米颗粒(〜20 nm)通过锂诱导的转化被电化学转化为超小直径(2-5 nm)的纳米颗粒时,催化活性的改善。反应。与大多数传统的化学合成方法不同,此方法可在纳米粒子之间保持出色的电互连,并导致较大的表面积和许多催化活性位点。我们证明锂诱导的超小NiFeOx纳米颗粒是活性双功能催化剂,对碱中的总水分解具有较高的活性和稳定性。在两电极配置和1 M KOH中,我们仅在1.51 V的条件下就可在10 mA cm-2的水分解电流中持续200 h以上,而不会降低性能,优于铱和铂作为基准催化剂的组合。

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