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Rapid Synthesis and Correlative Measurements of Electrocatalytic Nickel/Iron Oxide Nanoparticles

机译:电催化镍/氧化铁纳米粒子的快速合成和相关测量

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Electrocatalytic core-shell nanoparticles, such as nickel/iron oxides for the oxygen evolution reaction (OER) in alkaline electrolytes, require rapid synthesis and measurement for practical use. To meet this challenge, we investigated a novel process of adding Ni(II) species to Fe nanoparticles immediately after synthesis, which we expected to yield Ni-rich shells around Fe-rich cores. Cyclic voltammetry showed that the overpotential decreased as the molar ratio of Ni to Fe in the synthesis vessel increased from 0.2?mol Ni:1?mol Fe to 1.5?mol Ni:1?mol Fe, consistent with an increase of Ni composition. Unexpectedly, the overpotential increased abruptly at 2.0?mol Ni:1?mol Fe. X-ray photoelectron spectroscopy revealed that this synthesis ratio resulted in less Ni at the nanoparticle surfaces than lower synthesis ratios. These results demonstrate the sensitivity of rapid electrochemical measurements to surface composition, and the limits of Ni(II) adsorption and reduction to rapidly form Ni-rich shells around Fe-rich cores. Cyclic voltammetry also showed that the onset of the methanol oxidation reaction (MOR) correlates with the oxidation of Ni(OH)2 to NiOOH. Therefore, tuning materials to improve performance as OER catalysts also improves their performance as MOR catalysts.
机译:电催化核 - 壳纳米颗粒,例如碱性电解质中氧化反应(Oer)的镍/氧化铁,需要快速合成和测量以进行实际使用。为了满足这一挑战,我们研究了合成后立即将Ni(II)种类添加到Fe纳米颗粒的新方法,我们预计将在Fe-Rich核心周围产生富含Ni的壳。循环伏安显示,随着合成血管中Ni至Fe的摩尔比从0.2Ω·摩尔Ni:1?摩尔Fe增加到1.5摩尔Ni:1?摩尔Fe,与Ni组合物的增加一致。出乎意料的是,过电位突然增加2.0?Mol Ni:1?Mol Fe。 X射线光电子能谱显示,该合成比在纳米颗粒表面的少于较低的合成比率下导致较少的Ni。这些结果证明了快速电化学测量到表面组成的敏感性,以及Ni(II)的吸附和减少的限制,以快速形成Fe富含Fe的核心的富含Ni的壳。循环伏安还表明,甲醇氧化反应(MOR)的开始与Ni(OH)2至NiOOH的氧化相关。因此,调整材料以提高性能作为OER催化剂也改善了它们作为MOR催化剂的性能。

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