Jakub P. Masnica , Syed Sibt-e-Hassan , Sanja Potgieter-Vermaak , Yagya N. Regmi , Laurie A. King , Lubomira Tosheva
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引用次数: 0
摘要
使用旋转盘电极装置,在酸性(0.5 M H2SO4)和碱性(0.1 M KOH)电解质中考察了碳化 ZIF-8 (CZ) 及其掺杂铁的衍生物 CZ-A(掺杂硫酸铁(II)铵)和 CZ-B(掺杂醋酸铁(II))的氧还原反应(ORR)活性。这些数据表明,掺铁催化剂的 ORR 活性高于纯 CZ,在碱性电解质中的活性高于酸性电解质。广泛的材料表征突显了样品结晶度、形态、孔隙率和化学成分与所配置前驱体的重要差异。所制备催化剂的性能还受到铁前驱体选择的影响,这凸显了此类合成参数在控制 Fe-Nx 活性位点密度和识别方面的重要性。这些结果证明了掺铁碳化 ZIF-8 催化剂在碱性电解质中 ORR 的潜在应用,并为未来设计非贵金属燃料电池电催化剂提供了重要知识。
ZIF-8-derived Fe-C catalysts: Relationship between structure and catalytic activity toward the oxygen reduction reaction
The oxygen reduction reaction (ORR) activity of carbonized ZIF-8 (CZ) and its Fe-doped derivatives, CZ-A (doped with ammonium iron (II) sulphate) and CZ-B (doped with iron (II) acetate), were examined in both acidic (0.5 M H2SO4) and basic (0.1 M KOH) electrolytes using a rotating disk electrode setup. These data show that the ORR activity of the Fe-doped catalysts is higher than that of pure CZ, with a higher activity in basic than acidic electrolyte. Extensive materials characterization highlights important differences in the sample crystallinity, morphology, porosity, and chemical composition as a function of the deployed precursor. The performance of the prepared catalysts is also impacted by the Fe precursor selection, highlighting the importance of such synthetic parameters in controlling the density and identify of Fe-Nx active sites. These results demonstrate the potential application of Fe-doped carbonized ZIF-8 catalysts for the ORR in basic electrolyte and offer important knowledge for the future design of non-precious metal fuel cell electrocatalysts.