Synthesis of Carbon Supported Pd-Sn Catalysts by Ethylene Glycol Method for Ethanol Electrooxidation

被引:7
|
作者
Li, Yunhua [1 ]
Wang, Yajun [1 ]
Mao, Hongmin [2 ]
Li, Qiaoxia [1 ]
机构
[1] Shanghai Univ Elect Power, Coll Environm & Chem Engn, Shanghai Key Lab Mat Protect & Adv Mat Elect Powe, 2103 Pingliang Rd, Shanghai 200090, Peoples R China
[2] Wuhan Prod Qual Supervis & Testing Inst, 5 Donger Rd, Wuhan 430048, Hubei, Peoples R China
来源
关键词
ethanol electrooxidation; ethylene glycol method; Pd-based; Sn doping; FORMIC-ACID OXIDATION; ONE-STEP SYNTHESIS; ONE-POT SYNTHESIS; ALKALINE MEDIA; ELECTROCATALYTIC ACTIVITY; ROOM-TEMPERATURE; NANOPARTICLES; PERFORMANCE; REDUCTION;
D O I
10.201964/2016.08.18
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Carbon supported Pd-Sn catalysts (Pd-Sn/C-EG) were synthesized by an ethylene glycol method. The resulting catalysts exhibited high electrical catalytic activity for ethanol oxidation in alkaline solution. Transmission electron microscopyanalys was showed that the prepared Pd-Sn catalysts were uniformly dispersed on the carbon support with a mean particle size of 1.63 nm. X-ray diffraction patterns for all samples indicated a fcc crystalline structure. The negative shift observed for Pd (111) suggested that Sn could shrink the Pd crystalline lattice. The electrocatalytic activity and long-term stability towards ethanol electrooxidation of the Pd-Sn/C-EG catalyst were superior to that of a commercially available 20 wt.% Pd/C. More importantly, the oxidation peak current of the Pd-Sn/C-EG was found to be twice as large compared with that of Pd/C. This difference may be attributed to the uniform distribution of the prepared nanoparticles and the third body effect induced by addition of Sn onto the Pd surface. Furthermore, Sn doping can significantly provide the adsorption of OH species and speed up the ethanol oxidation reaction.
引用
收藏
页码:7011 / 7019
页数:9
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