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首页> 外文期刊>Electrochimica Acta >Synthesis and characterization of MoO{sub}x-Pt/C and TiO{sub}x-Pt/C nano-catalysts for oxygen reduction
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Synthesis and characterization of MoO{sub}x-Pt/C and TiO{sub}x-Pt/C nano-catalysts for oxygen reduction

机译:用于氧还原的MoO {sub} x-Pt / C和TiO {sub} x-Pt / C纳米催化剂的合成与表征

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The oxygen reduction reaction (ORR) was studied at carbon supported MoO{sub}x-Pt/C and TiO{sub}x-Pt nanocat-alysts in 0.5 moldm{sup}(-3) HClO{sub}4 solution, at 25℃. The MoO{sub}x-Pt/C and TiO{sub}x-Pt/C catalysts were prepared by the polyole method combined by MoO{sub}x or TiO{sub}x post-deposition. Home made catalysts were characterized by TEM and EDX techniques. It was found that catalyst nanoparticles were homogenously distributed over the carbon support with a mean particle size about 2.5 nm. Quite similar distribution and particle size was previously obtained for Pt/C catalyst. Results confirmed that MoO{sub}x and TiO{sub}x post-deposition did not lead to a significant growth of the Pt nanoparticles. The ORR kinetics was investigated by cyclic voltammetry and linear sweep voltammetry at the rotating disc electrode. These results showed the existence of two E - logj regions, usually observed with poly-crystalline Pt in acid solution. It was proposed that the main path in the ORR mechanism on MoO{sub}x-Pt/C and TiO{sub}x-Pt/C catalysts was the direct four-electron process with the transfer of the first electron as the rate-determining step. The increase in catalytic activity for ORR on MoO{sub}x-Pt/C and TiO{sub}x-Pt/C catalysts, in comparison with Pt/C catalyst, was explained by synergetic effects due to the formation of the interface between the platinum and oxide materials and by spillover due to the surface diffusion of oxygen reaction intermediates.
机译:在含碳的MoO {sub} x-Pt / C和TiO {sub} x-Pt纳米催化剂在0.5molm {sup}(-3)HClO {sub} 4溶液中于70℃下研究了氧还原反应(ORR)。 25℃。 MoO {sub} x-Pt / C和TiO {sub} x-Pt / C催化剂是采用MoO {sub} x或TiO {sub} x后沉积相结合的多元醇方法制备的。自制的催化剂通过TEM和EDX技术进行了表征。发现催化剂纳米颗粒均匀分布在碳载体上,平均粒径为约2.5nm。先前对于Pt / C催化剂获得了相当相似的分布和粒度。结果证实,MoO {sub} x和TiO {sub} x的后沉积不会导致Pt纳米粒子的显着生长。通过循环伏安法和线性扫描伏安法在旋转圆盘电极上研究了ORR动力学。这些结果表明存在两个E-logj区,通常在酸性溶液中用多晶Pt观察到。有人提出在MoO {sub} x-Pt / C和TiO {sub} x-Pt / C催化剂上进行ORR机理的主要途径是直接四电子过程,其中第一电子的转移速率为-确定步骤。与Pt / C催化剂相比,ORO在MoO {sub} x-Pt / C和TiO {sub} x-Pt / C催化剂上的催化活性增加是由协同效应引起的,这是由于铂和氧化物材料,以及由于氧气反应中间体的表面扩散而产生的溢出。

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