Department of Chemistry, University of Pretoria, Pretoria 0002, South Africa.
Phys Chem Chem Phys. 2013 Dec 28;15(48):20982-91. doi: 10.1039/c3cp52601a.
Palladium based nano-alloys are well known for their unique electrocatalytic properties. In this work, a palladium-decorated FeCo@Fe/C core-shell nanocatalyst has been prepared by a new method called microwave-induced top-down nanostructuring and decoration (MITNAD). This simple, yet efficient technique, resulted in the generation of sub-10 nm sized FeCo@Fe@Pd nanocatalysts (mainly 3-5 nm) from a micron-sized (0.21-1.5 μm) FeCo@Fe/C. The electrocatalytic activities of the core-shell nanocatalysts were explored for methanol oxidation reaction (MOR) and oxygen reduction reaction (ORR) in alkaline medium. A negative shift of 300 mV in the onset potential for MOR was observed, with a current thrice that of the Pd/C catalysts. A very low resistance to electron transfer (Rct) was observed while the ratio of forward-to-backward oxidation current (If/Ib) was doubled. The overpotential of ORR was significantly reduced with a positive shift of about 250 mV and twice the reduction current density was observed in comparison with Pd/C nanocatalysts with the same mass loading. The kinetic parameters (in terms of the Tafel slope (b) = -59.7 mV dec(-1) (Temkin isotherm) and high exchange current density (jo) = 1.26 × 10(-2) mA cm(-2)) provide insights into the favorable electrocatalytic performance of the catalysts in ORR in alkaline media. Importantly, the core-shell nanocatalyst exhibited excellent resistance to possible methanol cross-over during ORR, which shows excellent promise for application in direct alkaline alcohol fuel cells (DAAFCs).
钯基纳米合金以其独特的电催化性能而闻名。在这项工作中,通过一种称为微波诱导自上而下纳米结构化和装饰(MITNAD)的新方法制备了钯修饰的 FeCo@Fe/C 核壳纳米催化剂。这种简单而有效的技术导致从微米级(0.21-1.5 μm)的 FeCo@Fe/C 生成亚 10nm 大小的 FeCo@Fe@Pd 纳米催化剂(主要为 3-5nm)。在碱性介质中,对核壳纳米催化剂的电催化活性进行了甲醇氧化反应(MOR)和氧还原反应(ORR)的探索。观察到 MOR 的起始电位负移 300mV,电流是 Pd/C 催化剂的三倍。观察到电子转移电阻(Rct)非常低,而正向-反向氧化电流比(If/Ib)增加了一倍。与具有相同质量负载的 Pd/C 纳米催化剂相比,ORR 的过电位显著降低,正向移动约 250mV,还原电流密度增加了一倍。动力学参数(以 Tafel 斜率(b)=-59.7 mV dec(-1)(Temkin 等温线)和高交换电流密度(jo)=1.26×10(-2)mA cm(-2))表明催化剂在碱性介质中对 ORR 的有利电催化性能。重要的是,核壳纳米催化剂在 ORR 过程中对甲醇交叉的可能具有出色的抵抗力,这为其在直接碱性醇燃料电池(DAAFC)中的应用提供了广阔的前景。