Fabrication of hollow platinum-ruthenium core-shell catalysts with nanochannels and enhanced performance for methanol oxidation

被引:26
作者
Hu, Yuming [1 ]
Zhu, Aimei [1 ]
Zhang, Qiugen [1 ]
Liu, Qinglin [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem & Biochem Engn, Natl Engn Lab Green Chem Prod Alcohols Ethers & E, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
Methanol oxidation; Core-shell structure; Hollow; Nanochannel; Electrocatalyst; FACILE SYNTHESIS; ADVANCED NANOELECTROCATALYST; GALVANIC REPLACEMENT; CARBON-MONOXIDE; PT-CU; ELECTROOXIDATION; TIO2; ELECTROCHEMISTRY; NANOMATERIALS; SPHERES;
D O I
10.1016/j.jpowsour.2015.09.021
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
This work reports the preparation of hollow PtRu core shell catalysts with TiO2 as template, in which the Pt nanoparticles (NPs) grow on the exterior surface of Ru layer. The quantity of Pt NPs is easily tailored to control the integrity of Pt shell through varying the concentration of H2PtCl(6) solution. Scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and selected-area electron diffraction (SAED) are used to characterize the structure and morphology of H-PtRu. The core shell structure is confirmed by the high-angle annular dark-field scanning TEM (HAADF-STEM) with energy-disperse X-ray spectroscopy (EDX). The electrochemical performance of H-PtRu is investigated by cyclic voltammetry and chronoamperometry. Results show that the catalytic activity of H-PtRu toward methanol oxidation reaction (MOR) is similar to 2.5 times higher than that of Pt/C (JM), and the electrocatalytic stability improves with the increase of Ru content. Furthermore, H-PtRu exhibits better stability for methanol oxidation compared to Pt/C (JM) and PtRu/C (JM). (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:443 / 450
页数:8
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