熔盐合成用于析氧反应的增加(100)面和多晶氧化镍纳米颗粒:面和结晶度对电催化的影响

Darius W. Hayes, Elliot Brim, Konstantin Rücker, Dereje Hailu Taffa, Omeshwari Bisen, Marcel Risch, Shaun M. Alia, Jullian Lorenz, Corinna Harms, Michael Wark and Ryan M. Richards
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引用次数: 0

摘要

采用熔盐合成法合成了表面形貌增加(100)的氧化镍纳米立方(NiO(100)),并对其析氧反应(OER)活性进行了研究,探讨了表面形貌与OER性能之间的关系。在改变合成参数以减小NiO(100)颗粒尺寸和团聚的同时,使用Li2O作为Lux-Flood碱(标记为Li2O-MSS NiO,其中MSS代表熔盐合成)形成了多晶NiO纳米颗粒体系。进一步阐述了该合成方法,并对所得材料进行了OER活性测试。在进行了全面的结构表征以确定结晶度、晶格间距和元素分布后,在三电极旋转圆盘电极(RDE)系统中比较了它们与高表面积NiO(111)纳米片的OER活性。观察了(111)> li20 - mss >(100)的活性变化趋势。纳米立方和多晶样品活性的下降可以解释为理论和实验条件的差异、油墨流变性和由此产生的催化剂层性质的差异,以及在样品成像中看到的显著团聚。最后讨论了提高这些样品OER活性的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molten salt synthesis of increased (100)-facet and polycrystalline nickel oxide nanoparticles for the oxygen evolution reaction: impact of facet and crystallinity on electrocatalysis†

Molten salt synthesis of increased (100)-facet and polycrystalline nickel oxide nanoparticles for the oxygen evolution reaction: impact of facet and crystallinity on electrocatalysis†

Nickel oxide nanocubes with increased (100) surface facet presence (NiO(100)) were synthesized through a molten salt synthesis procedure to probe their oxygen evolution reaction (OER) activity in order to investigate the relationship between the surface facet and OER performance. While altering the synthesis parameters to decrease NiO(100) particle sizes and agglomeration, a polycrystalline NiO nanoparticle system formed from using Li2O as a Lux–Flood base (labelled Li2O-MSS NiO, where MSS stands for molten salt synthesis). This novel synthesis was further elaborated and the obtained materials were also tested for OER activity. After thorough structural characterization to determine crystallinity, lattice spacings, and elemental distribution, their OER activity was compared versus high surface area NiO(111) nanosheets in a three-electrode rotating disk electrode (RDE) system. The activity trend of (111) > Li2O-MSS > (100) was observed. This decrease in activity of the nanocube and polycrystalline samples was explained by differences between theoretical and experimental conditions, differences in ink rheology and resulting catalyst layer properties, and significant agglomeration seen in the imaging of the sample. Methods for improving the OER activity of these samples are discussed in the conclusion of this study.

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