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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Comprehensive Analysis on the Highly Active and Stable PdAu/C Electrocatalyst for Ethanol Oxidation Reaction in Alkaline Media
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Comprehensive Analysis on the Highly Active and Stable PdAu/C Electrocatalyst for Ethanol Oxidation Reaction in Alkaline Media

机译:碱性介质中乙醇氧化反应高活性稳定的PDAU / C电催化综合分析

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摘要

Both the catalytic activity and stability of palladium toward the ethanol oxidation reaction (EOR) in alkaline media are urgently required to be enhanced for the practical application of anion exchange membrane direct ethanol fuel cells (AEM DEFCs). The considerable improvement in the stability induced by the Au element has been well demonstrated; however, the catalytic activity from combining Pd with Au remains unsatisfied. Here, we successfully synthesize a series of PdxAuy/C electrocatalysts with different Pd/Au atomic ratios by a coreduction method, and in contrast to normal acknowledgments, the optimal PdAu/C sample not only possesses good stability but also has strikingly improved activity toward the EOR in alkaline media. Results show that the peak current density and degradation percentage for PdAu/C are, respectively, 84.16 mA/cm(2) and 12% and 59.73 mA/cm(2) and 67% for the pure Pd/C sample. It is anticipated that the striking activity toward the EOR can be attributed to an antipoisoning effect electronically induced by the Au addition, while the good stability can be ascribed to the formation of the stable Pd1Au1 alloy phase. It is also surprisingly revealed by physiochemical and electrochemical characterizations that there exists an unexpected monotone increasing trend for the promoting effect of Au content on Pd, and the compromise between the surface area specific activity and the number of active sites leads to the fact that the PdAu/C sample with Pd/Au atomic ratio of 1:1 has the highest mass activity toward the EOR in alkaline media.
机译:迫切需要提高阴离子交换膜直接乙醇燃料电池(AEM Defcs)的实际应用,迫切需要增强肺氧化反应(EOR)的催化活性和稳定性。 Au元素诱导的稳定性的相当大的改善得到了很好的证明;然而,与Au组合PD的催化活性仍然不满足。在这里,我们通过计算机方法成功地用不同的PD / AU原子比合成了一系列的PDxauy / C电催化剂,与正常致密相比,最佳PDAU / C样品不仅具有良好的稳定性,而且对其的活动引起了显着改善的活动碱性介质中的EOR。结果表明,PDAU / C的峰值电流密度和降解百分比,分别为84.16mA / cm(2)和12%和59.73mA / cm(2)和67%的纯Pd / C样品。预计朝向EOR的撞击活动可以归因于通过AU添加的电子诱导的抗磷酸效果,而良好的稳定性可以归因于稳定的PD1au1合金相的形成。它也令人惊讶的是通过物理化学和电化学表征揭示了一种意外的单调越来越多的趋势,即Au含量对Pd的促进作用,以及表面积特异性活动与活性场所数量之间的折衷会导致PDAU的事实/ C具有Pd / Au原子比为1:1的样品对碱性介质的EOR具有最高的质量活性。

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    Shanghai Jiao Tong Univ Inst Fuel Cells Sch Mech Engn 800 Dongchuan Rd Shanghai 200240 Peoples R China;

    Shanghai Jiao Tong Univ Inst Fuel Cells Sch Mech Engn 800 Dongchuan Rd Shanghai 200240 Peoples R China;

    Shanghai Jiao Tong Univ Inst Fuel Cells Sch Mech Engn 800 Dongchuan Rd Shanghai 200240 Peoples R China;

    Shanghai Jiao Tong Univ Inst Fuel Cells Sch Mech Engn 800 Dongchuan Rd Shanghai 200240 Peoples R China;

    Shanghai Jiao Tong Univ Inst Fuel Cells Sch Mech Engn 800 Dongchuan Rd Shanghai 200240 Peoples R China;

    Shanghai Jiao Tong Univ SJTU ParisTech Elite Inst Technol 800 Dongchuan Rd Shanghai 200240 Peoples R China;

    Shanghai Jiao Tong Univ Inst Fuel Cells Sch Mech Engn 800 Dongchuan Rd Shanghai 200240 Peoples R China;

    Shanghai Jiao Tong Univ Inst Fuel Cells Sch Mech Engn 800 Dongchuan Rd Shanghai 200240 Peoples R China;

    Shanghai Jiao Tong Univ Inst Fuel Cells Sch Mech Engn 800 Dongchuan Rd Shanghai 200240 Peoples R China;

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  • 正文语种 eng
  • 中图分类 物理化学(理论化学)、化学物理学;
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