首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >Structure, surface chemistry and electrochemical de-alloying of bimetallic PtxAg100-x nanoparticles: Quantifying the changes in the surface properties for adsorption and electrocatalytic transformation upon selective Ag removal
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Structure, surface chemistry and electrochemical de-alloying of bimetallic PtxAg100-x nanoparticles: Quantifying the changes in the surface properties for adsorption and electrocatalytic transformation upon selective Ag removal

机译:Bimetallic PTXAG100-X纳米粒子的结构,表面化学和电化学除合金化:在选择性Ag去除时量化吸附和电催化转化的表面性能变化

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摘要

We investigated the structure and surface chemistry of bimetallic PtAg nanoparticles, which were prepared by a water-in-oil microemulsion synthesis procedure, as well as the changes therein induced by electrochemical (surface) de-alloying, by a combination of electrochemical and in situ FTIR and online differential electrochemical mass spectrometry (DEMS) measurements. Based on transmission electron microscopy the resulting nanoparticles have a narrow size distribution with a mean diameter of around 6 nm, and increasing Ag contents lead to a broadening of the particle size distribution and a loss of the preferential formation of {100} facets observed for Pt nanoparticles. Evaluation of the hydrogen adsorption and CO oxidation characteristics and of the CO adsorption properties (IR) reveals detailed information on the surface composition of the bimetallic nanoparticles before and after electrochemical de-alloying, including also the distribution of Pt and Ag atoms in the surface. Furthermore, relevant information about the modifications in the chemical properties of Pt atoms/sites induced by the presence of Ag is extracted. For the as-prepared nanoparticles we find Ag surface enrichment, while de-alloying results in a core-shell structure with a PtAg core and a Pt shell, whose chemical properties are close to, but not identical, with those of polycrystalline Pt. More general, the study demonstrates that H-upd measurements are not suitable to identify the Pt surface content in such kind of bimetallic nanoparticles. (C) 2016 Elsevier B.V. All rights reserved.
机译:我们研究了双金属PTAG纳米颗粒的结构和表面化学性质,这是由一个水包油微乳液的合成方法制备,以及所述变化通过电化学(表面)在其中诱导脱合金化,通过组合的电化学和原位FTIR和网上差分电化学质谱(DEMS)测量。根据透射电子显微镜得到的纳米颗粒具有与纳米大约6的平均直径的窄粒度分布,以及增加的Ag含量导致粒度分布变宽和优先形成{100}的损失方面观察到铂纳米粒子。和氢吸附的评价CO氧化特性和CO吸附性能的(IR)显示前和后的双金属纳米颗粒的表面组成的详细资料电化学脱合金,还含有Pt和Ag的原子在表面上的分布。此外,在左右的Pt原子的化学性质的修改相关信息/通过Ag的存在诱导的位点被提取。对于所制备的纳米颗粒,我们发现银表面富集,而在芯 - 壳结构的脱合金的结果与芯PTAG和Pt壳,其化学性质接近,但不相同,与这些多晶Pt构成。更一般地,研究表明,H-UPD测量不适合于识别在此类双金属纳米粒子的表面的Pt含量。 (c)2016 Elsevier B.v.保留所有权利。

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