Effect of Co-catalyst on the Selective Electrooxidation of Glycerol over Ruthenium-based Nanomaterials

被引:33
|
作者
Palma, Livia M. [1 ]
Almeida, Thiago S. [1 ]
Morais, Claudia [2 ]
Napporn, Teko W. [2 ]
Kokoh, K. Boniface [2 ]
de Andrade, Adalgisa R. [1 ]
机构
[1] Univ Sao Paulo, Dept Quim, Fac Filosofia Ciencias & Letras Ribeirao Preto, Ave Bandeirantes 3900, BR-14040901 Ribeirao Preto, SP, Brazil
[2] Univ 8 Poitiers, UMR CNRS 7285, IC2MP, 4 Rue Michel Brunet B27,TSA 51106, F-86073 Poitiers 9, France
来源
CHEMELECTROCHEM | 2017年 / 4卷 / 01期
基金
巴西圣保罗研究基金会;
关键词
analytical methods; electrocatalysis; nanostructures; oxidation; ruthenium; ETHANOL FUEL-CELL; PT-RU; CARBON NANOTUBES; ELECTROCATALYTIC OXIDATION; METHANOL ELECTROOXIDATION; PLATINUM NANOPARTICLES; CO ELECTROOXIDATION; PTRU/C CATALYSTS; PD; ALLOYS;
D O I
10.1002/celc.201600406
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Ruthenium-based Pd and Pt nanoparticles were prepared by mild microwave-assisted heating and were characterized by X-ray diffraction and transmission electron microscopy. The activities of these catalysts during the oxidation of glycerol in alkaline media were studied by electrochemical, analytical, and insitu spectroscopy techniques. Changing the noble metal (Pd or Pt) allowed the selectivity of the catalysts to be tailored during the electrooxidation of glycerol. This introduces the possibility of utilizing the catalysts in cogeneration processes for renewable energy sources and also of employing the catalysts to produce value-added molecules selectively. High-performance liquid chromatography evidenced that the PtRu material had excellent catalytic activity in the selective oxidation of glycerol to dihydroxyacetone, whereas the PdRu anode favored the production of glycerate.
引用
收藏
页码:39 / 45
页数:7
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