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Enhancement of Nitrite and Nitrate Electrocatalytic Reduction through the Employment of Self-Assembled Layers of Nickel- and Copper-Substituted Crown-Type Heteropolyanions

机译:通过使用镍和铜取代的冠型杂多阴离子自组装层增强亚硝酸盐和硝酸盐的电催化还原

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摘要

Multilayer assemblies of two crown-type type heteropolyanions (HPA), [Cu20Cl(OH)(24)(H2O)(12)(P8W48O184)](25-) and Ni-4(P8W48O148)(WO2)](28-), have been immobilized onto glassy carbon electrode surfaces via the layer-by-layer (LBL) technique employing polycathion-stabilized silver nanoparticles (AgNP) as the cationic layer within the resulting thin films characterized by electrochemical and physical methods. The redox behaviors of both HPA monitored during LBL assembly with cyclic voltammetry and impedance spectroscopy revealed significant changes by immobilization. The presence of AgNPs led to the retention of film porosity and electronic conductivity, which has been shown with impedance and voltammeric studies of film permeabilities toward reversible redox probes. The resulting films have been characterized by physical methods. Finally, the electrocatalytic performance of obtained films with respect to nitrite and nitrate electrocatalytic reduction has been comparatively studied for both catalysts. Nickel atoms trapped inside HPA exhibited a higher specific activity for reduction.
机译:两个冠型杂杂阴离子(HPA)[[Cu20Cl(OH)(24)(H2O)(12)(P8W48O184)](25-)和Ni-4(P8W48O148)(WO2)](28-)的多层组件已通过层间固定(LBL)技术将聚四氟乙烯固定在玻璃碳电极表面上,该方法采用了聚阳离子稳定的银纳米颗粒(AgNP)作为所得薄膜内的阳离子层,其特征在于电化学和物理方法。用循环伏安法和阻抗谱法在LBL组装过程中监测的HPA的氧化还原行为显示出固定化的显着变化。 AgNPs的存在导致了薄膜孔隙率和电子传导性的保留,这已通过对可逆氧化还原探针的薄膜渗透性的阻抗和伏安研究得到了证明。所得膜已通过物理方法表征。最后,已对两种催化剂相对于亚硝酸盐和硝酸盐电催化还原的所得膜的电催化性能进行了比较研究。 HPA内捕获的镍原子具有更高的还原比活。

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