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Improved carbonate formation from ethanol oxidation on nickel supported Pt-Rh electrode in alkaline medium at room temperature

机译:室温下碱性介质中镍负载的Pt-Rh电极上乙醇氧化可改善碳酸盐形成

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In search for catalysts capable to oxidize small alcohols completely to CO32- in alkali, a few nickel supported platinum-rhodium (Pt-Rh) binary electrodes of varying mutual composition have been constructed by galvanostatic co-deposition of Pt-Rh on Ni support from suitable precursors' solutions. The co-deposited particles are found to lie in the nano-size domain by electron microscopy. Catalyst with approximately 35 atom% of Rh shows the highest electrocatalytic activity among the various compositions of the binary Ni/PtRh catalyst system studied for anodic oxidation of ethanol. Ex-situ FTIR studies show that molar ratio of the two products CO32- and CH3COO- in sequence, is increased on increasing the content of Rh in the binary deposit. Extended studies of ethanol, acetaldehyde and acetate at low concentrations reveal that electrochemically produced M-OH is responsible for chemical oxidations of organic fuels and related intermediates. The results lead to develop a proposed mechanism for the reaction. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
机译:为了寻找能够将小分子醇完全氧化为碱中的CO32-的催化剂,通过将Pt-Rh恒流共沉积在Ni载体上,构造了一些互不相同的镍负载铂铑(Pt-Rh)二元电极。合适的前体溶液。通过电子显微镜发现共沉积的颗粒位于纳米尺寸域中。在对乙醇进行阳极氧化研究的二元Ni / PtRh二元催化剂体系的各种组成中,具有约35原子%Rh的催化剂显示出最高的电催化活性。异位FTIR研究表明,随着二元矿床中Rh含量的增加,两种产物CO32-和CH3COO-的摩尔比依次增加。对低浓度乙醇,乙醛和乙酸盐的扩展研究表明,电化学生产的M-OH负责有机燃料和相关中间体的化学氧化。结果导致开发出提出的反应机理。 Hydrogen Energy Publications,LLC版权所有(C)2015。由Elsevier Ltd.出版。保留所有权利。

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