4.7 Article

Design of nanocatalyst for electrode structure: Electrophoretic deposition of iron phosphide nanoparticles to produce a highly active hydrogen evolution reaction catalyst

期刊

CHEMICAL ENGINEERING JOURNAL
卷 431, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.133217

关键词

Proton exchange membrane water electrolyzer; Hydrogen evolution reaction; Gas diffusion electrode; Electrophoretic deposition; Transition metal phosphide nanoparticle

资金

  1. Hydrogen Energy Innovation Technology Development Program through the National Research Foundation of Korea (NRF) - Ministry of Science and ICT (MSIT) [NRF-2019M3E6A1063676]
  2. Basic Science Research Program through the NRF - Ministry of Education [NRF-2019R1C1C1010137]
  3. NRF - Korea government (MSIT) [2020R1A5A1018052]

向作者/读者索取更多资源

In this study, we report a powerful manufacturing technique for fabricating an electrode with high hydrogen evolution reaction activity. By altering the deposition kinetics, the surface morphology and porosity of the electrode were tuned, leading to excellent performance.
The inherent properties of nanoparticles (NPs) can be engineered into macroscopic structures by capturing the collective characteristics of the nanomaterials via a fabrication process to realize macroscopic functionality. Herein, we report a powerful manufacturing technique for fabricating an electrode composed of highly porous iron phosphide (FeP) NP catalyst layers conformally deposited on macroporous Carbon paper (CP) that shows excellent hydrogen evolution reaction activity. The surface morphology and porosity of the FeP NP catalyst layers on the FeP/CP electrode were tuned by altering the deposition kinetics of the colloidal FeP NPs by controlling the solvent system in the electrophoretic deposition process. The FeP/CP electrode achieved a low overpotential of 38 mV at 10 mA cm(-2) in 0.5 M H2SO4 due to the highly exposed catalytic surface with a high catalyst loading amount and fast charge transfer. When the FeP/CP electrode was applied as a cathode gas diffusion electrode in a proton exchange membrane water electrolyzer, the single-cell exhibited excellent operating performance (1.48 A cm(-2) @ 2.0 V-cell, 90 degrees C). Our results illustrate a facile route for fabricating nanostructured macroscale devices by maximizing the collective properties of the nanoscale materials.

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