我们为生产单个水晶的 mesoporous 表明一个灵巧的热水的一个壶合成方法有空内部、多孔的表面结构的 PtPd 二金属的 nanoparticles 面对 Br - 并且我 - 离子。形成过程分析显示 Br - 的共存并且我 - 离子为新奇二金属的 nanoparticles 的形成负责。在离子与不同卤化物离子由协作完成了的磅和 Pd 金属的减小潜力的变化作为在 Pd 2+ 之间的流电的反应导致了空内部的形成,磅 4+ 离子发生了。另外, mesoporous PtPd nanoparticles 的尺寸能被稍微改变数量很好控制我 - 离子使用了。电气化学的测试显示水晶的 mesoporous PtPd 空 nanoparticles 展出了的 assynthesized 单身者作为与商业磅黑人和 Pt/C 材料相比向甲醇和乙醇氧化反应提高了催化性质。
We demonstrate a facile hydrothermal one-pot synthesis method for producing single crystalline mesoporous PtPd bimetallic nanoparticles with a hollow interior and porous surface structure in the presence of Br- and F ions. The formation process analysis indicated that the coexistence of Br- and I- ions is responsible for the formation of the novel bimetallic nanoparticles. The changes in the reduction potential of Pt and Pd metal ions achieved by the coordination with different halide ions resulted in the formation of hollow interiors as a galvanic reaction between Pd2~ and Pt4. ions occurred. In addition, the size of the mesoporous PtPd nanoparticles can be well controlled by slightly changing the amount of I- ions used. The electrochemical tests indicated that the as- synthesized single crystalline mesoporous PtPd hollow nanoparticles exhibited enhanced catalytic properties toward methanol and ethanol oxidation reactions as compared with the commercial Pt black and Pt/C materials.