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Improving Oxygen Reduction Reaction Activities on Carbon-Supported Ag Nanoparticles in Alkaline Solutions

机译:改善碱性溶液中碳载银纳米粒子的氧还原反应活性

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Carbon-supported Ag (Ag/C) catalysts with four different metal loadings were prepared by a citrate-protecting method. Oxygen reduction reaction (ORR) activities on these carbon-supported Ag-nanocatalysts (Ag/C) in alkaline solutions were studied. Four major findings are reported in this paper: (1) Test results indicate that the Ag/C catalysts promote predominately a four-electron pathway for ORR on electrodes over the swept potentials from 0.2 to -0.8 V vs Hg/HgO in O2-saturated 0.1 M NaOH solutions. (2) A novel marker for predicting ORR activities on the Ag/C catalysts based on the cyclic voltammetry characteristic curves has been identified: the ORR activities have a strong correlation with the intensity of the anodic peak at the potential of 0.230 V vs Hg/HgO in Ar-saturated 0.1 M NaOH solutions. (3) As the metal loading on carbon particles increases from 10 to 60 wt %, the peak intensities increase linearly, and the ORR onset potentials shift positively with maximum shift of 62 mV for 60% Ag on carbon support. (4) A hitherto unnoticed poisoning effect has been discovered: silicate has a significant poisoning effect on the ORR activities of the Ag/C catalysts.
机译:通过柠檬酸盐保护法制备了具有四种不同金属负载量的碳载银(Ag / C)催化剂。研究了碱性溶液中这些碳载银纳米催化剂(Ag / C)的氧还原反应(ORR)活性。本文报道了四个主要发现:(1)测试结果表明,在从O2饱和的Hg / HgO到0.2到-0.8 V的扫描电势上,Ag / C催化剂主要促进电极上ORR的四电子途径0.1 M NaOH溶液。 (2)已发现一种基于循环伏安法特性曲线预测Ag / C催化剂上ORR活性的新标记:ORR活性与0.230 V vs.Hg /的电势下的阳极峰强度密切相关。 HgO在Ar饱和的0.1 M NaOH溶液中。 (3)当碳颗粒上的金属负载量从10 wt%增加到60 wt%时,峰强度线性增加,并且碳载体上60%Ag的ORR起始电位正向移动,最大位移为62 mV。 (4)迄今尚未发现的中毒作用:硅酸盐对Ag / C催化剂的ORR活性具有显着的中毒作用。

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