首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Effect of Rh content on carbon-supported PtRh catalysts for dehydrogenative electrooxidation of cyclohexane to benzene over polymer electrolyte membrane fuel cell
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Effect of Rh content on carbon-supported PtRh catalysts for dehydrogenative electrooxidation of cyclohexane to benzene over polymer electrolyte membrane fuel cell

机译:Rh含量对高分子电解质膜燃料电池上环己烷脱氢电氧化为苯的碳载PtRh催化剂的影响

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摘要

Electrochemical dehydrogenative oxidation of cyclohexane to benzene was studied over carbon-supported PtRh(PtRh/C)electrocatalysts,which were prepared with different Pt:Rh atomic ratios from 4:1 to 1:4 using a borohydride reduction method combined with freeze-drying procedure at room temperature.The bimetallic PtRh/C catalysts were characterized by various physicochemical analyses such as X-ray diffraction(XRD),transmission electron microscopy(TEM),and X-ray absorption-near-edge spectroscopy(XANES).The variation of Rh content over the PtRh alloy formation caused significant structural and electronic modifications on the catalyst phase,which could be associated with consistent changes in electrocatalytic activities over a polymer electrolyte membrane(PEM)fuel cell.The Pt4Rh1/C catalyst as the anode electrocatalyst showed a maximum power density of ca.8.5 mW cm~(-2).Here,both the structural modification via lattice parameter change and the electronic modification through charge transfer from Rh to Pt could kinetically facilitate the sluggish electrode reaction with an increased exchange current density on the dehydrogenative electrooxidation of cyclohexane to benzene over the PtRh/C anodes of cyclohexane fuel cell.
机译:研究了碳载PtRh(PtRh / C)电催化剂上环己烷的电化学脱氢氧化为苯的过程,该催化剂采用硼氢化物还原法结合冷冻干燥法,以4:1至1:4的不同Pt:Rh原子比制备通过多种物理化学分析方法对双金属PtRh / C催化剂进行了表征,例如X射线衍射(XRD),透射电子显微镜(TEM)和X射线吸收近边光谱(XANES)。 PtRh合金形成过程中的Rh含量引起了催化剂相的显着结构和电子改性,这可能与聚合物电解质膜(PEM)燃料电池的电催化活性的恒定变化有关.Pt4Rh1 / C催化剂作为阳极电催化剂显示出最大功率密度约为8.5 mW cm〜(-2)。在这里,既可以通过晶格参数改变进行结构修改,也可以通过电荷转移进行电子修改在环己烷燃料电池的PtRh / C阳极上,从Rh到Pt的Rh到Pt可以动力学地促进缓慢的电极反应,交换电流密度增加,环己烷脱氢电氧化为苯。

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