首页> 外文会议>Polymer Electrolyte Fuel Cells 12 >Pt-Sn(oxidized shell)/C and Pt-Sn(reduced)/C as Cathode Catalysts For The Oxygen Reduction Reaction in Polymer Electrolyte Fuel Cells: Catalyst Performances and Characterization
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Pt-Sn(oxidized shell)/C and Pt-Sn(reduced)/C as Cathode Catalysts For The Oxygen Reduction Reaction in Polymer Electrolyte Fuel Cells: Catalyst Performances and Characterization

机译:Pt-Sn(氧化壳)/ C和Pt-Sn(还原)/ C作为聚合物电解质燃料电池中氧还原反应的阴极催化剂:催化剂性能和表征

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摘要

To address the problems (high price, insufficient total activity and deactivation) related to usage of pure Pt as cathode catalysts for oxygen reduction reactions (ORR) in polymer electrolyte fuel cells (PEFC), carbon-supported Pt-Sn(oxidized shell)/C and Pt-Sn(reduced)/C were used as membrane electrode assembly (MEA) cathode catalysts in PEFC. I-V-load curves in the initial load-cycles showed an increase of the performance for Pt-Sn(oxidized shell)/C, but no increase in the performance was observed with Pt-Sn(reduced)/C and standard Pt/C catalysts. The observed increase in the performance for the Pt-Sn(oxidized shell)/C catalyst may be due to an synergy effect of Pt-nanoparticle core and SnO_x-cluster shell formed on the Pt nanoparticle surface. In-situ XAFS at Pt Lm-edge and Sn K-edge under the PEFC operating conditions showed the absence of electron transfer from Sn to Pt and also no changes in the Sn state, indicating its stability. The in situ XAFS for the Pt-Sn(oxidized shell)/C also revealed that Pt nanoparticles made Pt-O bondings at higher voltages than 1.0 V vs. RHE, but the coordination number of Pt-0 bonds was much smaller than that for Pt/C. Thus, the Pt-Sn(oxidized shell)/C is a promising candidate as a MEA cathode catalyst in a PEFC system.
机译:为了解决与将纯Pt用作聚合物电解质燃料电池(PEFC)中的氧还原反应(ORR)的阴极催化剂,碳载Pt-Sn(氧化壳)/相关的问题(价格高,总活性不足和失活)/ C和Pt-Sn(还原)/ C用作PEFC中的膜电极组件(MEA)阴极催化剂。初始负载循环中的IV负载曲线表明Pt-Sn(氧化壳)/ C的性能有所提高,但Pt-Sn(还原)/ C和标准Pt / C催化剂的性能未见提高。观察到的Pt-Sn(氧化壳)/ C催化剂性能的提高可能归因于Pt纳米颗粒核和在Pt纳米颗粒表面形成的SnO_x簇壳的协同作用。在PEFC操作条件下,Pt Lm-edge和Sn K-edge处的原位XAFS显示不存在从Sn到Pt的电子转移,Sn状态也没有变化,表明其稳定性。 Pt-Sn(氧化壳)/ C的原位XAFS还显示,Pt纳米粒子在高于RHE的1.0 V电压下形成Pt-O键,但Pt-0键的配位数比RHE小得多。铂/碳。因此,Pt-Sn(氧化壳)/ C是有前途的候选物,可作为PEFC系统中的MEA阴极催化剂。

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  • 来源
    《Polymer Electrolyte Fuel Cells 12》|2012年|1651-1657|共7页
  • 会议地点 Honolulu HI(US)
  • 作者单位

    Innovation Research Center for Fuel Cells, The University of Electro-Communications, Chofu, Tokyo 182-8585, Japan;

    Innovation Research Center for Fuel Cells, The University of Electro-Communications, Chofu, Tokyo 182-8585, Japan;

    Innovation Research Center for Fuel Cells, The University of Electro-Communications, Chofu, Tokyo 182-8585, Japan;

    Innovation Research Center for Fuel Cells, The University of Electro-Communications, Chofu, Tokyo 182-8585, Japan;

    Innovation Research Center for Fuel Cells, The University of Electro-Communications, Chofu, Tokyo 182-8585, Japan;

    Innovation Research Center for Fuel Cells, The University of Electro-Communications, Chofu, Tokyo 182-8585, Japan;

    Faculty for Integrated Arts and Sciences, The University of Tokushima, Minamijosanjima, Tokushima 770-8506, Japan;

    Innovation Research Center for Fuel Cells, The University of Electro-Communications, Chofu, Tokyo 182-8585, Japan,JASRI/SPring-8, Sayo-cho, Sayo-gun, Hyogo 679-5198, Japan;

    Innovation Research Center for Fuel Cells, The University of Electro-Communications, Chofu, Tokyo 182-8585, Japan,Department of Engineering Science, Graduate School of Information Engineering Science, The University of Electro-Communications, Chofu, Tokyo 182-8585, Japan;

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