Oxidation of ethanol on carbon-supported oxide-rich Pd-W bimetallic nanoparticles in alkaline media

被引:2
作者
Liu, Tengfei [1 ]
Guo, Zengfeng [1 ]
Li, Wenpeng [1 ]
Pang, Zongjie [1 ]
Tong, Qingzhe [1 ]
机构
[1] Qilu Univ Technol, Inst Adv Energy Mat & Chem, Sch Chem & Pharmaceut Engn, Key Lab Fine Chem Univ Shandong, Jinan 250353, Shandong, Peoples R China
关键词
electrocatalysts; oxide-rich Pd-W alloy; alkaline media; ethanol oxidation reaction; OXYGEN REDUCTION REACTION; FORMIC-ACID ELECTROOXIDATION; DEMONSTRATE HIGH-ACTIVITY; FUEL-CELLS; CATALYTIC-ACTIVITY; TUNGSTEN CARBIDE; HIGH-PERFORMANCE; ELECTROCATALYSTS; METHANOL; NI;
D O I
10.1134/S0036024417100363
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
Carbon-supported oxide-rich Pd-W bimetallic nanoparticles were prepared by chemical reduction methods. The existence of oxides in the electrocatalysts is confirmed by X-ray photoelectron spectrum (XPS) and high resolution transmission electron microscopy. XPS analysis indicates that the oxygen atoms account for about 50% of all the atoms in Pd-W bimetallic nanoparticles. Compared to Pd/C catalyst, the carbon-supported oxide-rich Pd-W bimetallic nanoparticles exhibit a better catalytic activity for the anode oxidation of ethanol in alkaline media. The onset potential of the as prepared oxide-rich Pd0.8W0.2/C catalyst (Pd: W = 8: 2, metal atom ratio) for ethanol oxidation is negative shifted about 90 mV comparing to Pd/C catalyst. The oxide-rich Pd-W/C electrocatalysts provide a new model of noble-metal/promoter system as an extreme case of making the promoter (WO3) closely adjacent to the noble metal (Pd) by fabricating nanoparticles containing both atom-clusters of oxides and the noble metal atoms.
引用
收藏
页码:1994 / 2001
页数:8
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