Improved Glycerol Electrooxidation at Carbon-Supported PdFe Bimetallic Catalysts

被引:1
作者
Bresciani, Guilherme Bueno [1 ]
Franco, Jefferson Honorio [1 ,2 ]
Kokoh, K. Boniface [3 ]
Napporn, Teko W. [3 ]
De Andrade, Adalgisa R. [1 ,2 ]
机构
[1] Univ Sao Paulo, Fac Philosophy Sci & Letters Ribeirao Preto, Dept Chem, BR-14040901 Ribeirao Preto, SP, Brazil
[2] UNESP, Natl Inst Alternat Technol Detect Toxicol Evaluat, Inst Chem, BR-14800900 Araraquara, SP, Brazil
[3] Univ Poitiers, IC2MP, UMR 7285,CNRS, TSA 51106,B27, F-86073 Poitiers 09, France
基金
巴西圣保罗研究基金会; 瑞典研究理事会;
关键词
ALCOHOL FUEL-CELLS; ETHANOL OXIDATION; STABILITY; ELECTROCATALYSTS; CHALLENGES;
D O I
10.1149/1945-7111/ad1066
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We have investigated glycerol electrooxidation at Pd/C and PdFe/C catalysts, synthesized by the microwave polyol decomposition method. Five different heating ramps were tested to provide active catalyst nanoparticles and desired metal loadings at 20 wt%. Introducing iron in the Pd/C catalyst composition improved the catalytic activity and stability of the anode. The PdFe/C catalysts presented greater oxidative capacity and contributed efficiently to the keeping of glycerol skeleton reaction products. The analytical techniques composed of liquid chromatography coupled with mass spectrometry (LC-MS) confirmed glycerate, glycolate, formate, tartronate, and oxalate as the main glycerol oxidation products. The bi-metallic catalysts (PdFe/C) harvested electrons from glycerol and produced energy more effectively than the catalyst without iron (Pd/C). Glycerol proved a potential platform for generating high value-added products and can be employed as a renewable clean energy source for electrosynthesis purposes and fuel cell applications.
引用
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页数:7
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