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The Mechanism for Ethanol Oxidation Reaction on SnO_2@Pt/C Core Shell Electrocatalyst

机译:SnO_2 @ Pt / C核壳电催化剂上乙醇氧化反应的机理

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In the present work we investigated the products distributions from ethanol oxidation reaction (EOR) in acid solutions using SnO_2@Pt/C core-shell, PtSn/C E-TEK and Pt/C E-TEK as electrocatalysts assisted by "in situ" ATR-FTIR technique to obtain information about EOR mechanism on these materials. All materials used were 20% (w/w) metal on carbon XC 72-R. From "in situ" ATR-FTIR experiments with ethanol 1.0 mol L~(-1) it can be seen that the SnO_2@Pt/C material led to CO_2 formation in great proportion, while that, in Pt/C E-TEK acetic acid and acetaldehyde were the main products. In the chronoamperometry experiments at 0.5 V (vs RHE), the mass current density for ethanol oxidation was higher using SnO_2@Pt/C when compared to Pt/C and PtSn/C E-tek.
机译:在当前的工作中,我们研究了使用SnO_2 @ Pt / C核壳,PtSn / C E-TEK和Pt / C E-TEK作为“原位”辅助电催化剂的酸性溶液中乙醇氧化反应(EOR)的产物分布。 ATR-FTIR技术可获取有关这些材料的EOR机制的信息。使用的所有材料都是碳XC 72-R上20%(w / w)的金属。从1.0 mol L〜(-1)乙醇的“原位” ATR-FTIR实验可以看出,SnO_2 @ Pt / C材料导致CO_2的形成比例很高,而在Pt / C E-TEK乙酸中酸和乙醛是主要产品。在0.5 V(vs RHE)的计时电流法实验中,与Pt / C和PtSn / C E-tek相比,使用SnO_2 @ Pt / C进行乙醇氧化的质量电流密度更高。

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  • 来源
    《Polymer Electrolyte Fuel Cells 11》|2013年|2231-2236|共6页
  • 会议地点 Boston MA(US)
  • 作者单位

    LEMN - Centro de Ciencias Naturais e Humanas, UFABC - Universidade Federal do ABC, CEP 09.210-170, Rua Santa Adelia 166, Bairro Bangu, Santo Andre, SP, Brazil;

    LEMN - Centro de Ciencias Naturais e Humanas, UFABC - Universidade Federal do ABC, CEP 09.210-170, Rua Santa Adelia 166, Bairro Bangu, Santo Andre, SP, Brazil;

    Institute de Quimica de Sao Carlos, Universidade de Sao Paulo, Caixa Postal 780, 13566-590 Sao Carlos, SP, Brazil;

    LEMN - Centro de Ciencias Naturais e Humanas, UFABC - Universidade Federal do ABC, CEP 09.210-170, Rua Santa Adelia 166, Bairro Bangu, Santo Andre, SP, Brazil;

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  • 正文语种 eng
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