Highly active carbon nanotube-supported Ru@Pd core-shell nanostructure as an efficient electrocatalyst toward ethanol and formic acid oxidation

被引:31
作者
Zhang, Xiao-Jie [1 ]
Zhang, Jun-Ming [1 ]
Zhang, Pan-Yu [1 ]
Li, Yang [1 ]
Xiang, Sheng [1 ]
Tang, Hua-Guo [1 ]
Fan, You-Jun [1 ]
机构
[1] Guangxi Normal Univ, Coll Chem & Pharmaceut Sci, Guangxi Key Lab Low Carbon Energy Mat, Guilin 541004, Peoples R China
基金
中国国家自然科学基金;
关键词
Ru@Pd core-shell structure; Carbon nanotubes; Ethanol oxidation; Formic acid oxidation; ONE-POT SYNTHESIS; ALKALINE MEDIA; FUEL-CELL; BIMETALLIC CATALYSTS; ALCOHOL OXIDATION; POLYOL METHOD; TIN OXIDE; ELECTROOXIDATION; NANOPARTICLES; METHANOL;
D O I
10.1016/j.mcat.2017.04.015
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
Herein, we report the facile synthesis of core-shell structured Ru@Pd/multi-walled carbon nanotube (MWCNT) catalyst via a two-step chemical reduction process without any surfactant and its electrocatalytic performance for ethanol and formic acid oxidation. X-ray diffraction (XRD) and transmission electron microscopy (TEM) results revealed that the Ru@Pd nanoparticles are quite uniformly distributed on the surface of MWCNT with an average particle size of 2.3 nm. X-ray photoelectron spectroscopy (XPS) analysis showed the strong charge transfer interaction between Pd and Ru atoms on catalytic surface. The electrochemical studies demonstrated that the Ru@Pd/MWCNT catalyst exhibits higher peak current density and significantly enhanced long-term stability toward the anodic oxidation of ethanol in alkaline medium. Its electro-catalytic activity for ethanol oxidation is 1.8 and 2.7 times higher than that of Pd/MWCNT and commercial Pd/C catalysts, respectively, indicating the high utilization of Pd in as-prepared Ru@Pd/MWCNT catalyst. Moreover, the Ru@Pd/MWCNT also presents the enhanced electrocatalytic activity for formic acid oxidation (FAO) in acidic medium. This study opens up a new way for the fabrication of Pd-based electrocatalysts with high performance and low cost. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:138 / 144
页数:7
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