School of Chemistry, University of Southampton, Southampton, Hampshire, SO16 7NS (United Kingdom).
ChemSusChem. 2013 Oct;6(10):1973-82. doi: 10.1002/cssc.201300208. Epub 2013 Sep 23.
Model carbon supported Pt and Pd electrocatalysts have been prepared using a high-throughput physical vapor deposition method. For Pt, metal particle sizes are controlled between 1.5-5.5 nm over 100 electrodes of an electrochemical screening chip, allowing the oxygen reduction reaction (ORR) activity of the catalysts to be determined simultaneously. The ORR-specific current density is observed to increase with increasing particle diameter up to approximately 4 nm, at which point the activity begins to level off. The reduction in ORR activity for particles below 4 nm is accompanied by a concomitant increase in the overpotential for surface reduction. The resulting mass activity exhibits a maximum for particles with diameters of approximately 3.5 nm. These results are consistent with results published recently for high area carbon-supported Pt catalysts. For Pd particles, both the specific current density and the mass-specific activity for the ORR are observed to increase with increasing particle diameter, with no distinct optimum observed. The implications for the optimization of Pt- or Pd-based ORR catalysts for proton exchange membrane fuel cell (PEMFC) applications are discussed.
采用高通量物理气相沉积方法制备了模型碳负载的 Pt 和 Pd 电催化剂。对于 Pt,在电化学筛选芯片的 100 多个电极上控制金属颗粒尺寸在 1.5-5.5nm 之间,从而可以同时确定催化剂的氧还原反应(ORR)活性。观察到 ORR 比电流密度随粒径的增加而增加,直至约 4nm,此时活性开始趋于平稳。对于粒径小于 4nm 的颗粒,ORR 活性的降低伴随着表面还原的过电势的相应增加。所得的质量活性对于直径约为 3.5nm 的颗粒表现出最大值。这些结果与最近发表的高面积碳负载 Pt 催化剂的结果一致。对于 Pd 颗粒,观察到 ORR 的比电流密度和质量比活性均随粒径的增加而增加,没有观察到明显的最佳值。讨论了对于质子交换膜燃料电池(PEMFC)应用的 Pt 或 Pd 基 ORR 催化剂的优化的影响。