Fujian Key Laboratory of Advanced Materials, Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (PR China).
ChemSusChem. 2015 Feb;8(3):486-94. doi: 10.1002/cssc.201403037. Epub 2014 Dec 11.
Pt-based bimetallic electrocatalysts hold great potential in the oxygen reduction reaction (ORR) in current fuel-cell prototypes. However, they also face challenges from drastic dealloying of less-noble metals and coalescence of small nanoparticles. Porous and structure-ordered nanotubes may hold the potential to improve the stability of bimetallic electrocatalysts. Herein, we report a method to prepare CuPt nanotubes and porous Cu3 Pt intermetallic nanorods through a controlled galvanic replacement reaction and heat treatment process. The effect of the geometric features and compositional segregation on the electrocatalysis of the ORR was clarified. The outstanding performance of the Cu3 Pt/C-700 catalyst in the ORR relative to that of CuPt/C-RT was mainly attributed to the nanoporosity of the catalyst, whereas the enhanced specific activity on CuPt/C-RT after potential cycling was attributed to the interaction between the CuPt alloyed core and the Pt shell in the tube wall.
基于 Pt 的双金属电催化剂在当前燃料电池原型中的氧还原反应 (ORR) 中具有巨大的潜力。然而,它们也面临着来自较不活泼金属的剧烈脱合金和小纳米颗粒的聚集的挑战。多孔和结构有序的纳米管有可能提高双金属电催化剂的稳定性。在此,我们报告了一种通过控制的电替换反应和热处理过程制备 CuPt 纳米管和多孔 Cu3Pt 金属间纳米棒的方法。阐明了几何特征和组成分凝对 ORR 电催化的影响。Cu3Pt/C-700 催化剂在 ORR 中的优异性能相对于 CuPt/C-RT,主要归因于催化剂的纳米多孔性,而在电位循环后 CuPt/C-RT 的增强比活性则归因于管壁中 CuPt 合金核与 Pt 壳之间的相互作用。