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Performance and In-Situ FTIR Evaluation of Pt-Sn/C Electrocatalysts with Several Pt : Sn Atomic Ratios for the Ethanol Oxidation Reaction in Acidic Media

机译:PT-SN / C电催化剂的性能和原位FTIR评价几种Pt:Sn原子比在酸性培养基中的乙醇氧化反应

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Pt-Sn/C electrocatalysts with nominal Pt : Sn atomic ratios of 1 : 1, 2 : 1 and 3 : 1 were synthesized via the polyol method. The effects of the atomic ratios on their catalytic activity for the ethanol oxidation reaction (EOR) in acidic media was evaluated and compared to a Pt/C electrocatalyst obtained by the same procedure. The differences in reaction mechanism between the alloys and Pt/C were elucidated by in-situ FTIR measurements. XRD characterization of the Pt-Sn/C electrocatalysts showed a degree of alloying ranging between 27 and 54 % (from Vegard's law), while crystallite sizes close to 2.2 nm were determined with the Scherrer equation. Pt : Sn atomic ratios of 1 : 1, 1.6 : 1 and 2.4 : 1 were found experimentally via EDS analysis, fairly close to the nominally expected values. Electrochemical evaluation indicated that the alloy having a 1 : 1 ratio has the highest electrocatalytic activity for EOR. In-situ FTIR characterization showed that the Pt-Sn/C alloys promote the oxidation of ethanol via a triple parallel pathway: one path involving the directly conversion of COL (linearly-bonded CO) to CO2, while the second proceeds via the reaction of AAL (acetaldehyde) into COL and later to CO2, and the third involves the formation of AA (acetic acid) from adsorbed acetate that may be produced from AAL. Such mechanism promoted the EOR at more negative potentials at the alloys, also delivering higher current densities, relative to Pt/C. Thus, the inclusion of Sn in the Pt structure enhanced the catalytic activity for the EOR in acidic media.
机译:Pt-Sn / C电催化剂具有标称Pt:Sn原子比为1:1,2:1和3:1通过多元醇方法合成。评价原子比对酸性介质中乙醇氧化反应(EOR)催化活性的影响,并与通过相同程序获得的PT / C电催化剂进行比较。通过原位FTIR测量阐明了合金与PT / C之间的反应机制之间的差异。 PT-SN / C电催化剂的XRD表征在27%至54%(来自VEGARD的定律)之间的合金化程度,而Scherrer方程测定了近2.2nm的微晶尺寸。 PT:SN原子比例为1:1,1.6:1和2.4:1通过EDS分析发现,相当接近名义上预期的值。电化学评价表明,具有1:1的合金的合金具有最高的EOR电催化活性。原位FTIR表征显示Pt-Sn / C合金通过三个平行通路促进乙醇的氧化:一条涉及直接转化COL(线性键合CO)至CO2的路径,而第二步骤通过反应AAL(乙醛)进入COL和后面的CO 2,第三次涉及从吸附的乙酸盐中形成AA(乙酸),其可以由AA1制备。这种机制在合金的更负面电位下促进EOR,也相对于PT / C提供更高的电流密度。因此,在Pt结构中包含Sn的Sn增强了酸性介质中EOR的催化活性。

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