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Rh-pt Bimetallic Catalysts: Synthesis, Characterization, Andcatalysis Of Core-shell, Alloy, And Monometallicrnnanoparticles

机译:Rh-pt双金属催化剂:核-壳,合金和单金属纳米粒子的合成,表征和催化

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摘要

Rh@Pt core-shell, RhPt (1:1) alloy, and Rh + Pt monometallic nanoparticles (NPs) were prepared using standard polyol reduction chemistry in ethylene glycol (EG) with standard inorganic salts and polyvinylpyrrolidine (PVP_(55000)) stabilizers. PVP-free colloids were also prepared but less stable than the PVP-protected NPs. Rh@Pt core-shell particles were prepared from 2.7, 3.3, and 3.9 nm Rh cores with varying shell thicknesses (~1 and ~2 ML). The particles were characterized by a combination of TEM, single-particle EDS, EDS line scans, XRD analysis, Debye Function simulations, FT-IR, and micro-Raman CO-probe experiments. The three different architectures were evaluated for preferential oxidation of CO in hydrogen (PROX) using 1.0 wt % Pt loadings in Al_2O_3 supports. For hydrogen feeds with 0.2% CO and 0.5% O_2 the Rh@Pt NP catalyst has the best activity with complete CO oxidation at 70 ℃ and very high PROX selectivity at 40 ℃ with 50% CO conversion.
机译:Rh @ Pt核壳,RhPt(1:1)合金和Rh + Pt单金属纳米颗粒(NPs)是在乙二醇(EG)中与标准无机盐和聚乙烯吡咯烷酮(PVP_(55000))稳定剂一起使用标准多元醇还原化学方法制备的。还制备了不含PVP的胶体,但稳定性不如PVP保护的NP。 Rh @ Pt核-壳颗粒由2.7、3.3和3.9 nm的Rh核制备而成,壳厚度不同(〜1和〜2 ML)。通过结合TEM,单颗粒EDS,EDS线扫描,XRD分析,德拜功能模拟,FT-IR和微拉曼CO探针实验对颗粒进行了表征。使用Al_2O_3载体中1.0 wt%的Pt负载,评估了三种不同的体系在氢气中优先氧化CO(PROX)。对于含0.2%CO和0.5%O_2的氢气进料,Rh @ Pt NP催化剂具有最佳的活性,在70℃时会发生完全CO氧化,在40℃时有50%的CO转化率时,PROX选择性很高。

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  • 来源
    《Journal of the American Chemical Society》 |2008年第51期|17479-17486|共8页
  • 作者

    Selim Alayoglu; Bryan Eichhorn;

  • 作者单位
  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:20:17

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