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Electrocatalytic Activity for Oxygen Reduction Reaction of Au Core/Pt Shell Catalysts

机译:Au核/ Pt壳催化剂对氧还原反应的电催化活性

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摘要

We succeeded in preparing Au nanoparticles-loaded carbon black (Au/CB) catalyst by using Au colloidal solutions, which were prepared by just bubbling CO gas in KAuCl_4 aqueous solutions including polyvinyl alcohol. After CO bubbling, the color of the solutions changed from light yellow to red-brown, and UV-VIS absorption spectra showed surface plasmon resonance (SPR) band due to the formation of Au colloid. The SPR peak shifted to lower wavelengths with decreasing KAuCl_4 concentration, indicating the formation of smaller Au particles. Transmission electron microscopy revealed that the Au nanoparticles loaded with CB have a mean size of 3.3 nm with a standard deviation of 0.7 nm; this mean particle size agrees with that estimated by X-ray diffraction. Pt monolayers were deposited on the Au/CB nanoparticles (Pt_x/Au/CB (x = number of monolayers)) by underpotential deposition. Cyclic voltammograms of the Pt_1/Au/CB nanoparticles indicate that 75% of the Au surface is covered with Pt. The activity per unit mass of Pt (mass activity) for the oxygen reduction reaction (ORR) for the Pt_1/Au/CB at 0.9 V was 5.1 times higher than that of commercial Pt/CB. In durability tests in which the potential was cycled between 0.6-1.0 V, Pt_1/Au/CB had a higher durability than commercial Pt/CB.
机译:我们通过使用Au胶体溶液成功制备了负载Au纳米颗粒的炭黑(Au / CB)催化剂,该胶体溶液是通过将CO气体鼓入包含聚乙烯醇的KAuCl_4水溶液制备的。 CO鼓泡后,溶液的颜色从浅黄色变为红棕色,并且由于形成Au胶体,UV-VIS吸收光谱显示出表面等离子体共振(SPR)带。随着KAuCl_4浓度的降低,SPR峰移至较低的波长,表明形成了较小的Au颗粒。透射电子显微镜显示,负载有CB的Au纳米颗粒的平均尺寸为3.3 nm,标准偏差为0.7 nm。该平均粒度与通过X射线衍射估计的粒度一致。通过欠电势沉积将Pt单层沉积在Au / CB纳米颗粒上(Pt_x / Au / CB(x =单层数))。 Pt_1 / Au / CB纳米颗粒的循环伏安图表明,Au表面的75%被Pt覆盖。在0.9 V下,Pt_1 / Au / CB的氧还原反应(ORR)的每单位质量Pt活性(质量活性)比市售Pt / CB高5.1倍。在电势在0.6-1.0 V之间循环的耐久性测试中,Pt_1 / Au / CB的耐久性高于商用Pt / CB。

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  • 来源
    《Polymer Electrolyte Fuel Cells 11》|2013年|2237-2243|共7页
  • 会议地点 Boston MA(US)
  • 作者单位

    Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Sakai, Osaka 599-8531, Japan;

    Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Sakai, Osaka 599-8531, Japan;

    Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Sakai, Osaka 599-8531, Japan;

    Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Sakai, Osaka 599-8531, Japan;

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  • 正文语种 eng
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