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Electrochemical promotion of gold nanoparticles supported on yttria-stabilized zirconia.

机译:氧化钇稳定的氧化锆上负载的金纳米粒子的电化学促进。

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摘要

The feasibility of highly dispersed gold nanocatalyst supported on yttria-stabilized zirconia (YSZ) for the model reactions of C2H4 and CO oxidation is demonstrated for the first time. Gold nanoparticles are synthesized on YSZ powder by chemical reduction of the precursor salt in the mixture of ethanol, water and polyvinylpyrrolidone (PVP). Resulting metal loading of the catalysts are 1 wt.% with average particle sizes ranging from 6 to 9 nm. Results of CO and C2H4 oxidation display catalytic activity at 65 °C and 25 °C for CO and C2H4 oxidation, respectively. The catalytic properties of the catalysts are different due to their average particle size. Electrochemical Promotion of Catalysis (EPOC) of C2H4 oxidation is demonstrated. Application of constant potential difference between two electrodes in the bipolar electrochemical cell led to increase in C2H4 conversion. A proposed mechanism explains the bipolar EPOC phenomenon through formation of O2- flux across the electrochemical cell, resulting in the change of Work Function of gold nanoparticles placed in between the electrodes and is electronically isolated.
机译:首次证明了在氧化钇稳定的氧化锆(YSZ)上负载的高分散金纳米催化剂对C2H4和CO氧化的模型反应的可行性。通过将乙醇,水和聚乙烯吡咯烷酮(PVP)的混合物中的前体盐进行化学还原,可以在YSZ粉末上合成金纳米颗粒。催化剂的金属负载量为1重量%,平均粒径为6至9nm。 CO和C2H4氧化的结果分别显示在65°C和25°C下对CO和C2H4氧化的催化活性。催化剂的催化性质由于它们的平均粒径而不同。证明了C2H4氧化的电化学催化促进(EPOC)。双极电化学电池中两个电极之间恒定电势差的施加导致C2H4转化率增加。拟议的机制通过在电化学电池中形成O2通量来解释双极性EPOC现象,从而导致置于电极之间的金纳米颗粒的功函数发生变化,并且被电子隔离。

著录项

  • 作者

    Kim, Jong Min.;

  • 作者单位

    University of Ottawa (Canada).;

  • 授予单位 University of Ottawa (Canada).;
  • 学科 Chemical engineering.;Inorganic chemistry.
  • 学位 M.A.Sc.
  • 年度 2011
  • 页码 149 p.
  • 总页数 149
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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