Murawska Magdalena, Cox James A, Miecznikowski Krzysztof
Department of Chemistry, University of Warsaw, Pasteura 1, PL-02-093 Warsaw, Poland.
Department of Chemistry and Biochemistry, Miami University, Oxford, OH 45056 USA.
J Solid State Electrochem. 2014;18(11):3003-3010. doi: 10.1007/s10008-014-2493-0. Epub 2014 May 10.
In this article, we characterized tungsten oxide-decorated carbon-supported PtIr nanoparticles and tested it for the electrooxidation reactions of ethylene glycol and ethanol. Phase and morphological evaluation of the proposed electrocatalytic materials are investigated employing various characterization techniques including X-ray diffraction (XRD) and transmission electron microscopy (TEM). Electrochemical diagnostic measurements such as cyclic voltammetry, chronoamperometry, and linear sweep voltammetry revealed that the tungsten oxide-modified PtIr/Vulcan nanoparticles have higher catalytic activity for ethylene glycol and ethanol electrooxidation than that of PtIr/Vulcan. A significant enhancement for electrooxidation of CO-adsorbate monolayers occurred in the presence of a transition metal oxide relative to that of pure PtIr/Vulcan electrocatalyst. The likely reasons for this are modification on the Pt center electronic structure and/or increasing the population of reactive oxo groups at the PtIr/Vulcan electrocatalytic interface in different potential regions.
在本文中,我们对氧化钨修饰的碳载PtIr纳米颗粒进行了表征,并测试了其对乙二醇和乙醇的电氧化反应性能。采用包括X射线衍射(XRD)和透射电子显微镜(TEM)在内的各种表征技术,对所提出的电催化材料进行了相和形态评估。循环伏安法、计时电流法和线性扫描伏安法等电化学诊断测量结果表明,氧化钨修饰的PtIr/炭黑纳米颗粒对乙二醇和乙醇电氧化的催化活性高于PtIr/炭黑。相对于纯PtIr/炭黑电催化剂,在过渡金属氧化物存在下,CO吸附单层的电氧化有显著增强。其可能的原因是在不同电位区域对Pt中心电子结构的修饰和/或增加了PtIr/炭黑电催化界面处活性氧基团的数量。