PtxIry alloy nanoparticles with fully tunable bulk and surface compositions

被引:12
作者
El Sawy, Ehab N. [1 ,2 ]
Handal, Hala T. [1 ,2 ]
Thangadurai, V. [1 ]
Birss, Viola I. [1 ]
机构
[1] Univ Calgary, Dept Chem, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada
[2] Natl Res Ctr, Phys Chem & Corros Lab, Cairo, Egypt
基金
加拿大自然科学与工程研究理事会;
关键词
CORE-SHELL NANOPARTICLES; CARBON-MONOXIDE; HYDROGEN ADSORPTION; PLATINUM-ELECTRODES; IRIDIUM ELECTRODES; PTIR NANOPARTICLES; IR NANOPARTICLES; OXIDATION; CATALYSTS; RU;
D O I
10.1039/c6ta06161c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
PtxIry nanoparticles (NPs) are of great interest, largely due to their wide range of applications in gas phase catalysis, electrocatalysis, sensors, and more. Most of the prior work on PtxIry NPs, formed using a variety of approaches, has shown that the surface becomes uncontrollably enriched with Pt relative to the NP bulk. In this work, PtxIry alloy NPs (with x and y (35-85%) being the atomic percent of Pt and Ir, respectively) were synthesized using the simple polyol method, using Pt and Ir solution precursors and employing two sequential heating steps. It is shown that this method prevents the enrichment of the surface with either Pt or Ir, resulting in the same surface and bulk compositions, fully controllable by modifying the ratio of metal precursors in solution. This was confirmed by electrochemical studies, wavelength dispersive X-ray spectroscopy (XRD), and energy dispersive X-ray spectroscopy (EDS) coupled with high resolution transmission electron microscopy (HRTEM), while XRD analysis confirmed PtxIry alloy formation. The predictable and tunable composition of these materials, both in the NP bulk and at their surfaces, is a novel and important advantage for their future use as catalysts and reagents for a broad range of reactions, including methanol oxidation, as demonstrated here.
引用
收藏
页码:15400 / 15410
页数:11
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