首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >The goldilocks electrolyte: examining the performance of ironickel oxide thin films as catalysts for electrochemical water splitting in various aqueous NaOH solutions
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The goldilocks electrolyte: examining the performance of ironickel oxide thin films as catalysts for electrochemical water splitting in various aqueous NaOH solutions

机译:金发姑娘的电解质:研究铁/氧化镍薄膜作为在各种NaOH水溶液中进行电化学水分解的催化剂的性能

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A rigorous study of electrodeposited pure and mixed Ni/Fe oxides was performed in three different sodium hydroxide electrolytes with various Fe impurity concentrations (<1 ppb, 5 ppb and 102 ppb). The presence and concentration of the Fe impurities in the three electrolytes is determined by Inductive Coupled Plasma spectroscopy. The rationale for investigating the OER performance of the pure and mixed Ni/Fe catalysts in various NaOH solutions, rather than the widely reported and more expensive KOH, with different Fe impurities was to conclude if the OER activity was comparable to the KOH and if the activity differed between NaOH solutions. A number of the mixed Ni/Fe catalysts in NaOH containing Fe impurities at a concentration of 5 ppb exhibited higher OER activities, with higher Turnover Frequency than the same catalyst in the NaOH solutions containing <1 ppb and 102 ppb and the state if the art RuO2. These Ni/Fe oxide materials are also cheaper to produce than the aforementioned platinum group materials therefore rendering these Ni/Fe catalysts more practical and economical. All of the material/electrolyte combinations are also evaluated with respect to their Tafel slopes and measured overpotential at a current density of 10 mA cm(-2). To determine the Ni and Fe species formed before and after OER ex-situ Raman spectroscopy and X-ray photoelectron spectroscopy are utilised. Interestingly, the oxidation state of the Ni species in the pure Ni material does not change during OER in any of the NaOH media. While for the pure Fe and mixed Ni/Fe 50/50 material, the oxidation states of the species vary with the concentration of Fe impurities in the NaOH solution.
机译:在三种具有不同铁杂质浓度(<1 ppb,5 ppb和102 ppb)的氢氧化钠电解液中,对电沉积的纯Ni / Fe和混合Ni / Fe混合氧化物进行了严格的研究。通过电感耦合等离子体光谱法确定三种电解质中铁杂质的存在和浓度。研究纯的和混合的Ni / Fe催化剂在各种NaOH溶液中的OER性能的原理(而不是广泛报道且价格昂贵的具有不同Fe杂质的KOH)的基本原理是得出结论,即OER活性是否与KOH相当,以及NaOH溶液的活性不同。与含<1 ppb和102 ppb的NaOH溶液中的相同催化剂相比,含Fe杂质浓度为5 ppb的NaOH中的许多混合Ni / Fe催化剂表现出更高的OER活性,具有更高的周转频率。 RuO2。这些Ni / Fe氧化物材料的生产也比上述铂族材料便宜,因此使这些Ni / Fe催化剂更加实用和经济。还评估了所有材料/电解质组合的Tafel斜率,并在10 mA cm(-2)的电流密度下测量了超电势。为了确定在OER异位拉曼光谱和X射线光电子能谱之前和之后形成的Ni和Fe物种。有趣的是,在任何NaOH介质中进行OER期间,纯Ni材料中Ni物种的氧化态都不会改变。而对于纯铁和混合的Ni / Fe 50/50材料,物质的氧化态随NaOH溶液中Fe杂质的浓度而变化。

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