Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/87279
Title: Ethylene glycol and ethanol oxidation on spinel ni-co oxides in alkaline
Authors: Xu, Zhichuan J.
Sun, Shengnan
Zhou, Ye
Hu, Benlin
Zhang, Qichun
Keywords: Ethanol
Oxides
DRNTU::Engineering::Materials
Issue Date: 2015
Source: Sun, S., Zhou, Y., Hu, B., Zhang, Q., & Xu, Z. J. (2016). Ethylene glycol and ethanol oxidation on spinel ni-co oxides in alkaline. Journal of The Electrochemical Society, 163(2), H99-H104. doi:10.1149/2.0761602jes
Series/Report no.: Journal of The Electrochemical Society
Abstract: This article presents a systematic study on the composition dependence of Ni-Co oxides (NCOs) on their electrocatalytic activities toward ethylene glycol (EG) and ethanol (EtOH) oxidation. NCO electrodes were prepared by co-electrodeposition method followed by annealing in air. The atomic ratios of Ni / (Ni + Co) (Ni content) in NCOs were controlled by adjusting the concentration ratio of Ni and Co precursors. As the Ni content increased, the phase of materials changed from the spinel to the mixture of spinel and rock salt. The electrocatalytic activities of these NCOs toward EG and EtOH oxidation were investigated by cyclic voltammetry, differential pulse voltammetry, multi-step chronoamperometry, and electrochemical impedance spectroscopy techniques. It was found that the performance of NCOs for EG and EtOH oxidation exhibited a firstly-increase-then-decrease trend with the increase of Ni content and the best performance was found at 46% Ni. The presence of Ni probably can facilitate EG and EtOH oxidation. Increasing the concentration of reactants or pH can improve the reaction rates. The products from EG and EtOH oxidation were analyzed by nuclear magnetic resonance, which indicated that the oxidation reaction was a process from hydroxyl group to carboxyl group.
URI: https://hdl.handle.net/10356/87279
http://hdl.handle.net/10220/48208
ISSN: 0013-4651
DOI: 10.1149/2.0761602jes
Rights: © 2015 The Electrochemical Society. All rights reserved. This paper was published in Journal of the Electrochemical Society and is made available with permission of The Electrochemical Society.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles

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