首页> 外文会议>Polymer Electrolyte Fuel Cells >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(减少)/ c作为聚合物电解质燃料电池中的氧还原反应的阴极催化剂:催化剂性能和表征

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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:以解决与纯铂的使用作为用于聚合物电解质燃料电池的氧还原反应(ORR)阴极催化剂(PEFC)的问题(价格高,总活性不足和失活),碳负载的Pt-Sn系(氧化壳)/ C和铂 - 锡(还原)/ C被用作膜电极组件在PEFC(MEA)阴极催化剂。在初始负载周期IV-负载曲线显示为铂 - 锡(氧化壳)/ C的性能的增加,但有Pt-Sn系(还原)/ C和标准Pt / C催化剂中观察到的性能不会增加。由于铂纳米颗粒芯和SnO_x簇壳形成的铂纳米颗粒表面上的协同效应所观察到的增加的铂 - 锡(氧化壳)/ C催化剂可以是性能。原位在PEFC运行条件下的Pt LM-边缘和Sn K边缘XAFS显示不存在选自Sn的电子转移到Pt中的,并且还没有改变Sn的状态,表明其稳定性。原位XAFS为铂 - 锡(氧化壳)/ C还透露,Pt纳米粒子在较高电压下由Pt-O的键所大于1.0 V,相对于RHE,但铂O键的配位数比为小得多的Pt / C。因此,在Pt-Sn系(氧化壳)/ C是有希望的候选如在PEFC系统中的MEA的阴极催化剂。

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