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首页> 外文期刊>Journal of combinatorial chemistry >Combinatorial Electrochemical Screening of Fuel Cell Electrocatalysts
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Combinatorial Electrochemical Screening of Fuel Cell Electrocatalysts

机译:燃料电池电催化剂的组合电化学筛选

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Combinatorial methods have been applied to the preparation and screening of fuel cell electrocatalysts.Hardware and software have been developed for fast sequential measurements of cyclic voltammetric and steady-state currents in 64-element half-cell arrays.The arrays were designed for the screening of high-surface-area supported electrocatalysts.Analysis software developed allowed the semiautomated processing of the large quantities of data,applying filters that defined figures of merit relevant to fuel cell catalyst activity and tolerance.Results are presented on the screening of carbon-supported platinum catalysts of varying platinum metal loading on carbon (and thus,particle size) in order to demonstrate the speed and sensitivity of the screening methodology.CO electro-oxidation,oxygen reduction,and methanol oxidation on a series of such catalysts reveal clear trends in characteristics and activities.Catalysts with smaller particle sizes reveal structure in the CO stripping voltammetry that can be associated with edge sites in addition to the closely packed planes,and this is concomitantly reduced as particle size is increased.Specific activity for steady-state methanol oxidation and oxygen reduction at room temperature in H_2SO_4 electrolyte is found to be a maximum for the largest particle sizes,in agreement with the literature.These trends in activity are significantly smaller than the differences in activities of promoted platinum-based alloy catalysts for the same reaction.
机译:组合方法已应用于燃料电池电催化剂的制备和筛选,并开发了硬件和软件以快速顺序测量64元素半电池阵列中的循环伏安和稳态电流。开发的分析软件允许半自动处理大量数据,应用定义了与燃料电池催化剂活性和耐受性有关的品质因数的过滤器。结果在筛选碳载铂催化剂时给出了结果。改变铂金属在碳上的负载量(进而改变粒径),以证明筛选方法的速度和灵敏度。在一系列此类催化剂上进行的CO电氧化,氧还原和甲醇氧化反应显示出明显的特性和粒径较小的催化剂显示出CO汽提伏安中的结构除紧密堆积的平面外,还可能与边缘位点相关的实验,并且随着粒径的增加而降低。在室温下,H_2SO_4电解质中稳态甲醇氧化和氧还原的比活最大对于最大粒径,与文献一致。这些活性的趋势明显小于相同反应中促进型铂基合金催化剂活性的差异。

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