γ-NiOOH对碱性溶液中氧还原和析氧反应的双功能催化活性

Ridwan P. Putra, I. B. Rachman, H. Horino, I. Rzeznicka
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引用次数: 4

摘要

众所周知,氢氧化镍(NiOOHs)在碱性溶液中对析氧反应(OER)具有优异的活性。然而,它们对氧还原反应(ORR)的活性在很大程度上尚未被探索。存在三种NiOOH多晶型:α-、β-和γ-NiOOH,其特征在于不同的层间距。尽管仍存在争议,但具有大层间距的γ-NiOOH已被指示为OER的活性相。本文通过镍二硫代草酰胺Ni(dto)在1M KOH溶液中的原位电化学转化,在碳基体中制备了高度结晶的γ-NiOOH。以这种方式制备的催化剂不仅对OER,而且在碱性溶液中对ORR都显示出低的过电位。相对于RHE,ORR的起始电位约为0.81V,反应通过2e−转移途径进行。高OER催化活性和相对低的ORR过电位使该纳米复合催化剂成为双功能OER/ORR催化剂的良好候选者,在碱性溶液中稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bifunctional Catalytic Activity of γ-NiOOH toward Oxygen Reduction and Oxygen Evolution Reactions in Alkaline Solutions
Nickel oxyhydroxides (NiOOHs) are well-known for their superior activity toward oxygen evolution reaction (OER) in alkaline solutions. However, their activity toward oxygen reduction reaction (ORR) has been largely unexplored. There exist three NiOOH polymorphs: α-, β-, and γ-NiOOH, characterized by different interlayer spacing. Although still debated, γ-NiOOH with a large layer spacing has been indicated as the active phase for OER. Here, a highly crystalline γ-NiOOH was prepared in a carbon matrix by the in situ electrochemical transformation of nickel dithiooxamide Ni(dto) in 1 M KOH solution. The catalyst prepared in this way showed low overpotential not only for OER, but also for ORR in alkaline solutions. The onset potential for ORR is ~0.81 V vs. RHE, and the reaction proceeds via the 2e− transfer pathway. The high OER catalytic activity and relatively low ORR overpotential make this nanocomposite catalyst a good candidate for bifunctional OER/ORR catalyst, stable in alkaline solutions.
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