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Highly active and sintering-resistant heteroepitaxy of Au nanoparticles on ZnO nanowires for CO oxidation

机译:纳米氧化锌在氧化锌纳米线上的高活性和耐烧结性

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摘要

Gold was supported on commercial ZnO powders (P) and homemade ZnO nanowires (NWs) by a modified deposition-precipitation method.X-ray diffraction and transmission electron microscopy investigation indicated that the size of the Au nanoparticles (NPs) depended strongly on the calcination temperature.The Au NPs were highly dispersed (< 5nm) on both supports with calcination temperatures < 400℃.However,after calcination at 600 ℃ the Au NPs aggregated much more severely on ZnO P than on ZnO NWs.Gold NPs epitaxially grew into the {10-10} facets of the ZnO NWs after calcination at temperatures > 400 ℃.Such unique anchoring mechanism accounts for the much better experimentally observed sintering resistance.X-ray photoelectron spectra showed that Au existed as both metallic Au0 and Auδ+ species in all the synthesized catalysts with or without calcination treatment;the ratios of Auδ+/Au0,however,varied,depending on the treatment conditions.Catalytic tests showed that the activity for CO oxidation strongly depended on the size of the Au NPs.After calcination at 600 ℃,the specific rate for CO oxidation at room temperature decreased about 30 times on Au/ZnO P but only about 4 times on Au/ZnO NW.Stability tests demonstrated that the Au/ZnO NW catalysts had better stability for CO oxidation.
机译:通过改进的沉积-沉淀法将金负载在商品ZnO粉末(P)和自制ZnO纳米线上(XW).X射线衍射和透射电子显微镜研究表明,金纳米颗粒(NPs)的大小强烈依赖于煅烧煅烧温度<400℃时,Au NPs高度分散(<5nm)。但是,在600℃煅烧后,Au NPs在ZnO P上的聚集比在ZnO NWs上严重得多。在> 400℃的温度下煅烧后,ZnO NW的{10-10}面。这种独特的锚固机制是实验观察到的更好的烧结抗性。X射线光电子能谱表明,Au以金属Au0和Auδ+的形式存在。所有合成的催化剂都经过或不经过煅烧处理;Auδ+ / Au0的比例随处理条件的不同而变化。催化试验表明,CO氧化活性在600℃煅烧后,室温下CO氧化的比速率在Au / ZnO P上降低了约30倍,而在Au / ZnO NW上仅降低了约4倍。稳定性测试表明: Au / ZnO NW催化剂具有较好的CO氧化稳定性。

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  • 来源
    《天然气化学(英文版)》 |2016年第3期|361-370|共10页
  • 作者单位

    College of Chemical Engineering and Technology, Harbin Institute of Technology, Harbin 150001, Heilongjiang, China;

    Department of Physics, Arizona State University, Tempe, Arizona 85287, USA;

    Department of Physics, Arizona State University, Tempe, Arizona 85287, USA;

    State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;

    Department of Physics, Arizona State University, Tempe, Arizona 85287, USA;

    State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;

    College of Chemical Engineering and Technology, Harbin Institute of Technology, Harbin 150001, Heilongjiang, China;

    Department of Physics, Arizona State University, Tempe, Arizona 85287, USA;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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