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首页> 外文期刊>Electrochimica Acta >Glucose electro-oxidation on Pt(100) in phosphate buffer solution (pH 7): A mechanistic study
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Glucose electro-oxidation on Pt(100) in phosphate buffer solution (pH 7): A mechanistic study

机译:磷酸盐缓冲溶液中Pt(100)的葡萄糖电氧化(pH7):机械研究

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Glucose is an important biomolecule that participates as a main source of energy in living organism reactions. Considering its biological importance, the electrochemical investigation about glucose electrooxidation has attracted attention with the aim to develop non-enzymatic catalysts able to achieve the complete oxidation of glucose to be used as fuel in Direct Glucose Fuel Cells (DGFC). However, there are some challenges related to the oxidation of this relatively large, complex molecule, such as product distributions, adsorbed species, surface poisoning and structure sensitivity that must be understood. The use of well-defined surfaces, as single crystals, is a helpful tool to progress in this knowledge. In this context, the goal of this manuscript is the elucidation of the glucose electro-oxidation reaction in phosphate buffered solution (pH 7) on Pt(100) using cyclic voltammetry and in situ FTIR techniques at room temperature. It was observed that the reaction product distribution depends on glucose concentration. The maximum current density was reached with 2 x 10(-2) mol dm(-3) glucose (similar to 2.04 mA cm(-2)) and then decreases with the increase of glucose concentration, because the reaction becomes dominated by the formation of strongly adsorbed species. In situ FITR experiments on Pt(100) show that the reaction proceeds through a complex mechanism, involving CO2, COL, COB, cyclic carbonate, gamma-lactone, delta-lactone and carboxylic acids as intermediates and/or oxidation products. CO2 is generated mainly from COB and cyclic carbonate. Adsorbed CO seems to be the poisoning species responsible of the decrease of the catalytic activity on Pt(100), especially in the linear configuration, at higher glucose concentration. (C) 2020 Elsevier Ltd. All rights reserved.
机译:葡萄糖是重要的生物分子参与在生物体反应的能量的主要来源。考虑到其生物学重要性,关于葡萄糖电氧化的电化学行为已引起重视,目的是开发能够达到葡萄糖完全氧化非酶催化剂被用作直接葡萄糖燃料电池(DGFC)燃料。但是,也有诸如产品分布,吸附的物质,表面中毒和结构灵敏度与此相关的相对大的,复杂的分子的氧化一些挑战,必须理解。使用定义良好的表面,如单晶,在这方面的知识进步的有用工具。在此背景下,本手稿的目标是葡萄糖电氧化在磷酸盐缓冲溶液(pH 7)在Pt(100),使用循环伏安法和原位FTIR技术在室温下反应的阐明。据观察,所述反应产物的分布取决于葡萄糖浓度。的最大电流密度,用2×10(-2)摩尔分米(-3)葡萄糖(类似于2.04毫安厘米(-2))达到了,然后与葡萄糖浓度的增加而减小,这是因为反应变成被形成为主强烈吸附的物质。在在Pt(100)原位FITR实验表明,通过复杂的机构进行反应,涉及CO 2,COL,COB,环状碳酸酯,γ-内酯,δ-内酯和羧酸作为中间体和/或氧化产物。 CO2主要产生从COB和环状碳酸酯。吸附的CO似乎是负责在Pt(100)的催化活性的降低的中毒物质,特别是在直链构型,在较高葡萄糖浓度。 (c)2020 elestvier有限公司保留所有权利。

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