Pd nanoparticles anchored on carbon-doped TiO2 nanocoating support for ethanol electrooxidation in alkaline media

被引:31
|
作者
Qin, Yuan-Hang [1 ]
Zhuang, Yan [2 ]
Lv, Ren-Liang [1 ]
Wang, Tie-Lin [1 ]
Wang, Wei-Guo [1 ]
Wang, Cun-Wen [1 ,3 ]
机构
[1] Wuhan Inst Technol, Minist Educ, Key Lab Green Chem Proc, Wuhan 430074, Peoples R China
[2] Jiangsu Univ Technol, Sch Chem & Environm Engn, Changzhou 213000, Peoples R China
[3] Wuhan Inst Technol, Hubei Key Lab Novel Chem Reactor & Green Chem Tec, Wuhan 430074, Peoples R China
基金
湖北省教育厅重点项目;
关键词
TiO2; nanocoating; Pd catalyst; ethanol oxidation; OXYGEN REDUCTION REACTION; ANATASE-TYPE TIO2; ELECTROCATALYTIC ACTIVITY; FUEL-CELLS; ALCOHOL OXIDATION; CATALYST SUPPORT; HYBRID MATERIALS; OXIDE; NANOTUBES; PALLADIUM;
D O I
10.1016/j.electacta.2014.12.050
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Carbon-doped TiO2 nanocoating (TiO2-C) on carbon black ( CB) was prepared and employed as the support of Pd catalyst for ethanol oxidation reaction (EOR) in alkaline media. The obtained catalyst was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and electrochemical measurements. TEM characterization shows that TiO2 nanocoating is formed uniformly on CB and still preserves its structure with no apparent sintering after carbon doping, and Pd particles are well dispersed on the conductive TiO2-C support. XRD characterization shows that TiO2- C presents an anatase structure. XPS characterization shows that oxygen vacancy defects resulting from carbon doping present in TiO2- C. Cyclic voltammetry (CV) and chronoamperometry (CA) results demonstrate that the as-prepared Pd/TiO2-C catalyst exhibits much enhanced catalytic activity and stability for EOR in alkaline media than Pd/C catalyst. The enhanced activity presented by the Pd/TiO2-C catalyst may result from the strong interactions between TiO2 and Pd, the facilitated oxidation removal of CH3COads intermediate, and the facilitated transportation of ethanol to Pd active sites. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:77 / 82
页数:6
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