4.7 Article

Unexpected facilitation of the pyrolysis products of potassium ferrocyanide to the electrocatalytic activity of a PdO based palladium iron composite catalyst towards ethanol oxidation reaction (EOR)

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 46, 期 1, 页码 633-644

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2020.10.009

关键词

Potassium ferrocyanide; Pyrolysis product; PdO-Based palladium iron catalyst; Ethanol oxidation reaction

资金

  1. Ministry of Science and Technology of China [2019YFE0100200, 2019YFA0705703]
  2. National Natural Science Foundation of China [U1564205]
  3. Technical Innovation Advanced Research Foundation of Hebei Normal University [L2018K03]

向作者/读者索取更多资源

The pyrolysis products of potassium ferrocyanide were found to significantly enhance the electrocatalytic activity of a PdO based palladium iron composite catalyst for ethanol oxidation reaction. Samples prepared with different amounts of K-4[Fe(CN)(6)] exhibited varied morphologies and electrocatalytic performance, with the addition of K-4[Fe(CN)(6)] resulting in improved catalytic activity.
It was found, for the first time, that the pyrolysis products of potassium ferrocyanide (K-4[Fe(CN)(6)]) could significantly promote the electrocatalytic activity of the PdO based palladium iron composite catalyst towards ethanol oxidation reaction (EOR). In this work, huge carbon spheres (abbreviated as HCSs) were prepared firstly via a pyrolysis method using glucose and 1-butyl-3-methylimidazolium tetrafluoroborate as the starting materials. Secondly, PdO based palladium iron composites supported on HCSs (noted as PdO-Pd -Fe/HCSs) were successfully fabricated through a pyrolysis procedure employing PdO center dot H2O, HCSs and K-4[Fe(CN)(6)] as the initial materials. When preparing PdOePdeFe/HCSs, four different amounts of K-4[Fe(CN)(6)] were respectively added in the preparation system producing four kinds of samples. The sample prepared in the absence of K-4[Fe(CN)(6)] was nominated as sample b-0. And the samples prepared in the presence of 5, 10 and 20 mg K-4[Fe(CN)(6)] were, respectively, labeled as sample b-5, b-10 and b-20. It was indicated by the XRD and XPS patterns that the metallic Pd particles were the main crystalline materials of above four samples. SEM images of all synthesized samples substantially demonstrated that the added amount of K-4[Fe(CN)(6)] was a pivotal factor which could significantly affect the morphologies of the prepared samples. For sample b-0, besides some nanoparticles with a size close to 30 nm, a larger number of pores were created on the surface of the HCSs producing a honeycomb-shaped surface. Interestingly, aniseed shaped particles, cauliflower-like particles and irregular particles with a diameter more than 150 nm were, respectively, anchored on the HCSs surface of sample b-5, b-10 and b-20. Most of all, as indicated by CV and CA measurements, all the samples prepared in the presence of K-4[Fe(CN)(6)] delivered much better electrocatalytic activities towards EOR when compared to the sample prepared with no addition of K-4[Fe(CN)(6)]. For example, in the CV curves, the peak current density of the peak appearing in the positive potential scanning (peak f) for EOR on sample b-10 was nearly 6.4 times greater than that on sample b-0 (16.6 mA cm(-2) vs. 2.6 mA cm(-2)). The significantly decreased charge transfer resistance and the remarkably enlarged electrochemical surface area were analyzed to be the main reasons for sample b10 to exhibit the best electrocatalytic performance among all prepared samples. In general, a novel electrocatalyst consisting of PdO, Pd and the pyrolysis products of K-4[Fe(CN)(6)] for EOR was developed in this work, which, due to its very lower preparation cost and its satisfied electrocatalytic activity towards EOR, was very helpful to the development of Pdbased EOR electrocatalyst. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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