4.7 Article

Surface fluorinated nickel-graphene nanocomposites for high-efficiency methanol electrooxidation

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 46, Issue 53, Pages 27138-27148

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2021.05.178

Keywords

Nickel; Silicon; Methanol oxidation; Fluorine; Graphene

Funding

  1. National Key Research and Development Program of China [2017YFA0204800]
  2. National MCF Energy RD Program [2018YFE0306105]
  3. National Natural Science Foundation of China [51902217, 91961120]
  4. Collaborative Innovation Center of Suzhou Nano Science and Technology
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions
  6. 111 Project
  7. Devices and Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX19_1924]

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The surface fluorinated nickel-graphene nano-composites synthesized via reduction of Si-H bonds in hydrothermal condition exhibit higher activity and kinetics for methanol oxidation reaction (MOR). The introduction of fluorine leads to the formation of nickelic, decreasing the reaction energy barrier for MOR. The strong electronegativity of fluorine atoms facilitates the attraction of OH- groups and repulsion of protons, contributing to the enhanced performance of F-Ni-G nanocomposites as MOR catalysts.
Transition metal electrocatalysts with high activity and long durability are desired for methanol oxidation reaction (MOR). Here, the surface fluorinated nickel-graphene nano-composites (F-Ni-G) are synthesized via the reduction of Si-H bonds produced by silicon and ammonium fluoride in hydrothermal condition. During this process, ionic nickel-F bonds and semi-ionic C-F bonds are introduced to the catalysts as confirmed by X-ray photoelectron spectroscopy. When F-Ni-G nanocomposites are employed as MOR catalysts, the surface fluorination is contributed to the formation of nickelic, which can increase the activity and kinetics for MOR. The onset oxidation potential of F-Ni-G-2 for methanol oxidation is 53 mV lower than that of the Ni/G catalyst without fluorine. The mass activity of F-Ni-G-2 (2493.3 A g(-1)) is 3.90 folds than that of Ni/G (638.5 A g(-1)). In addition, the density functional theory calculation indicates that the modified fluorine in graphene results in the decreased reaction energy barrier from *CO to *COOH step in MOR. The strong electronegativity of F atom makes intermediates easier to attract OH- groups and repel protons, which is conductive to decrease the reaction energy barrier for MOR. Such a facile method for the fabrication of the surface fluorinated catalytic system may be extended to the preparation of other transition metal electrocatalysts. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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