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Ethanol Electro-Oxidation on PtSn/C-ATO Electrocatalysts

机译:PtSn / C-ATO电催化剂上的乙醇电氧化

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PtSn/C-ATO electrocatalysts with different Pt:Sn atomic ratios (90:10, 70:30 and 50:50) were preparedin a single step by an alcohol-reduction process using H2PtCl6.6H2O and SnCl2.2H2O as metal sourcesand ethylene glycol as solvent and reducing agent and a physical mixture of carbon Vulcan XC72 (85wt%) and Sb2O5.SnO2 (15 wt%) as support (C-ATO). The obtained materials were characterized by X- ray diffraction (XRD) and transmission electron microscopy (TEM). The catalytic activity for ethanolelectro-oxidation in acid medium was investigated by cyclic voltammetry and chroamperometry and insingle direct ethanol fuel cell (DEFC). XRD analyses showed that Pt(fcc), SnO2, carbon and ATOphases coexist in the obtained materials. The electrochemical studies showed that PtSn/C-ATOelectrocatalysts were more active for ethanol electro-oxidation than PtSn/C electrocatalyst. Theo experiments at 100 C on a single DEFC showed that the power density of the cell using PtSn/C-ATO(90:10) was nearly 100% higher than the one obtained using PtSn/C (50:50). FTIR measurementsshowed that the addition of ATO to PtSn/C favors the formation of acetic acid as a product while forPtSn/C acetaldehyde was the principal product formed.
机译:通过使用H2PtCl6.6H2O和SnCl2.2H2O作为金属源和乙二醇的醇还原工艺一步一步制备具有不同Pt:Sn原子比(90:10、70:30和50:50)的PtSn / C-ATO电催化剂作为溶剂和还原剂,以及碳Vulcan XC72(85 wt%)和Sb2O5.SnO2(15 wt%)作为载体(C-ATO)的物理混合物。通过X射线衍射(XRD)和透射电子显微镜(TEM)表征获得的材料。通过循环伏安法和电流安培法以及单直接乙醇燃料电池(DEFC)研究了在酸性介质中乙醇电氧化的催化活性。 XRD分析表明,所得材料中共存有Pt(fcc),SnO2,碳和ATO相。电化学研究表明,PtSn / C-ATO电催化剂比PtSn / C电催化剂对乙醇的电氧化活性更高。在单个DEFC上于100 C进行的实验结果表明,使用PtSn / C-ATO(90:10)的电池的功率密度比使用PtSn / C(50:50)的电池的功率密度高近100%。 FTIR测量表明,在PtSn / C中加入ATO有利于乙酸的生成,而PtSn / C乙醛是生成的主要产物。

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