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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Synthesis and Comparative Study of Nanoporous Palladium-Based Bimetallic Catalysts for Formic Acid Oxidation
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Synthesis and Comparative Study of Nanoporous Palladium-Based Bimetallic Catalysts for Formic Acid Oxidation

机译:纳米多孔钯基双金属甲酸氧化催化剂的合成与比较研究

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In view of the inherent limitations of current portable technology energy sources, the implementation of micro fuel cells is becoming increasingly appealing. This has generated great interest in the development of direct formic acid micro fuel cells. In this study, nanoporous Pd and four nanoporous bimetallic Pd-M catalysts with an atomic ratio of 90:10, where M = Cd, Pb, Ir, and Pt, were synthesized via a facile hydrothermal method and examined for the electrochemical oxidation of formic acid. The electrocatalytic activity of these nanoporous electrode materials was studied with the use of linear sweep voltammetry and chronoamperometry. Our chronoamperometric measurements have shown that the initial electrochemical performance of the nanoporous Pd-M electrodes toward formic acid oxidation was almost independent of the alloying materials; however, the second incorporated metal strongly affected the stability of the Pd-based electrocatalysts. The mechanisms of the oxidation of formic acid were further examined with the aid of in situ electrochemical ATR-FTIR spectroscopy. For the nanoporous Pd, PdCd, and PdPb catalysts, oxidation proceeds through the direct mechanism, whereas the indirect mechanism, along with major CO poisoning, was observed in the case of the PdIr and PdPt catalysts. The incorporation of even small amounts of Pt and Ir to Pd was found to inhibit the oxidation of formic acid. On the other hand, the addition of Pb to Pd served to promote the direct mechanism, which in turn makes these Pd-based catalysts both cost and electrocatalytically more effective.
机译:鉴于当前便携式技术能源的固有局限性,微型燃料电池的实施变得越来越有吸引力。这对直接甲酸微型燃料电池的开发引起了极大的兴趣。在本研究中,通过简便的水热法合成了纳米孔Pd和四种原子比为90:10的纳米孔双金属Pd-M催化剂,其中M = Cd,Pb,Ir和Pt,并用于甲酸的电化学氧化酸。使用线性扫描伏安法和计时电流法研究了这些纳米多孔电极材料的电催化活性。我们的计时电流法测量表明,纳米多孔Pd-M电极对甲酸氧化的初始电化学性能几乎与合金材料无关;然而,第二种掺入的金属强烈影响了Pd基电催化剂的稳定性。借助原位电化学ATR-FTIR光谱进一步检查了甲酸的氧化机理。对于纳米多孔Pd,PdCd和PdPb催化剂,氧化是通过直接机理进行的,而在PdIr和PdPt催化剂的情况下,则观察到间接机理以及主要的CO中毒现象。发现即使将少量的Pt和Ir掺入Pd也会抑制甲酸的氧化。另一方面,将Pb添加到Pd中有助于促进直接机理,这又使这些基于Pd的催化剂在成本和电催化方面都更加有效。

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